U.S. patent application number 17/089570 was filed with the patent office on 2021-02-25 for scanning apparatus and methods useful for detection of chemical and biological analytes.
The applicant listed for this patent is Omniome, Inc.. Invention is credited to Dale Buermann, Michael John Erickstad, Rebecca McGinley, Alex Nemiroski, Arnold Oliphant, Harry Scott Rapoport.
Application Number | 20210054453 17/089570 |
Document ID | / |
Family ID | 1000005197182 |
Filed Date | 2021-02-25 |
View All Diagrams
United States Patent
Application |
20210054453 |
Kind Code |
A1 |
Buermann; Dale ; et
al. |
February 25, 2021 |
SCANNING APPARATUS AND METHODS USEFUL FOR DETECTION OF CHEMICAL AND
BIOLOGICAL ANALYTES
Abstract
An apparatus can include a vessel, a reference surface, a
preload, a scan actuator, and a transmitter. The reference surface
can form a structural loop with a detector. The preload can be
configured to urge the vessel to contact an area on the reference
surface. The scan actuator can be configured to slide the vessel
along the reference surface in a scan dimension. The transmitter
can be configured to direct signal from the vessel to a detector
and/or direct energy from an energy source to the vessel, when the
vessel is urged by the preload to contact the reference
surface.
Inventors: |
Buermann; Dale; (San Diego,
CA) ; Erickstad; Michael John; (San Diego, CA)
; McGinley; Rebecca; (San Diego, CA) ; Nemiroski;
Alex; (San Diego, CA) ; Rapoport; Harry Scott;
(San Diego, CA) ; Oliphant; Arnold; (Morgan Hill,
CA) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
Omniome, Inc. |
San Diego |
CA |
US |
|
|
Family ID: |
1000005197182 |
Appl. No.: |
17/089570 |
Filed: |
November 4, 2020 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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15998727 |
Aug 15, 2018 |
10858701 |
|
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17089570 |
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62545606 |
Aug 15, 2017 |
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Current U.S.
Class: |
1/1 |
Current CPC
Class: |
G01N 2021/0346 20130101;
B01L 2300/0877 20130101; B01L 3/502715 20130101; G01N 21/645
20130101; G01N 21/03 20130101; G01N 2021/0375 20130101; B01L
2400/0487 20130101; B01L 2300/1822 20130101; G01N 21/6428 20130101;
B01L 3/527 20130101; G01N 21/13 20130101; B01L 7/52 20130101; B01L
9/52 20130101; C12Q 1/6874 20130101; G01N 21/05 20130101; G01N
2021/6439 20130101 |
International
Class: |
C12Q 1/6874 20060101
C12Q001/6874; G01N 21/13 20060101 G01N021/13; B01L 3/00 20060101
B01L003/00; B01L 7/00 20060101 B01L007/00; G01N 21/64 20060101
G01N021/64; B01L 9/00 20060101 B01L009/00; G01N 21/03 20060101
G01N021/03 |
Claims
1-20. (canceled)
21. A method of scanning a vessel, comprising (a) translating a
vessel along a reference surface of a detection apparatus, wherein
the vessel comprises a lumen and a wall, wherein the lumen
comprises analytes, wherein the reference surface contacts at least
a portion of the vessel during the translating, and wherein the
reference surface forms a structural loop with a detector; and (b)
detecting the analytes at different locations along the vessel
using the detector, wherein the vessel is urged to the reference
surface by a preload during the detecting, thereby scanning the
vessel.
22. A method of scanning a vessel, comprising (a) examining a first
subset of analytes in a vessel while applying a preload to a first
portion of the vessel, wherein the preload positions the first
subset of analytes to occupy an xy plane in a detection zone,
wherein the preload is not applied to a second portion of the
vessel; (b) translating the vessel to position a second subset of
the analytes in the xy plane of the detection zone; and (c)
examining the second subset of the analytes in the vessel while
applying the preload to a second portion of the vessel, wherein the
preload positions the second subset of the analytes to occupy the
xy plane of the detection zone, wherein the preload is not applied
to the first portion of the vessel, thereby scanning the
vessel.
23. A reactor apparatus, comprising (a) a vessel comprising a lumen
and a wall, wherein the wall comprises an internal surface and an
external surface, wherein the internal surface contacts the lumen;
(b) a reference surface that forms a structural loop with an energy
source; (c) a preload configured to urge the external surface of
the vessel to contact an area on the reference surface; (d) a scan
actuator configured to slide the vessel along the reference surface
in a scan dimension; and (e) a transmitter configured to direct
energy from the energy source to the internal surface or the lumen
when the external surface of the vessel is urged by the preload to
contact the reference surface.
24. A method of performing reactions in a vessel, comprising (a)
translating a vessel along a reference surface of a reactor
apparatus, wherein the vessel comprises a lumen and a wall, wherein
the lumen comprises reactants, wherein the reference surface
contacts at least a portion of the vessel during the translating,
and wherein the reference surface forms a structural loop with an
energy source; and (b) directing energy from the energy source to
the reactants at different locations along the vessel, wherein the
vessel is urged to the reference surface by a preload during the
directing of the energy to the reactants, thereby performing
reactions in the vessel.
25. A method of performing reactions in a vessel, comprising (a)
delivering energy from a reactor apparatus to a first subset of
reactants in a vessel while applying a preload to a first portion
of the vessel, wherein the preload positions the first subset of
reactants to occupy an xy plane of a reaction zone, wherein the
preload is not applied to a second portion of the vessel; (b)
translating the vessel to position a second subset of the reactants
in the xy plane of the reaction zone; and (c) delivering energy
from the reactor apparatus to the second subset of the analytes in
the vessel while applying the preload to a second portion of the
vessel, wherein the preload positions the second subset of the
analytes to occupy the xy plane, wherein the preload is not applied
to the first portion of the vessel, thereby performing reactions in
the vessel.
Description
CROSS REFERENCE TO RELATED APPLICATION
[0001] This application is a divisional application of Ser. No.
15/998,727 filed Aug. 15, 2018, entitled "SCANNING APPARATUS AND
METHODS USEFUL FOR DETECTION OF CHEMICAL AND BIOLOGICAL ANALYTES,"
which claims priority to U.S. Provisional Application No.
62/545,606 filed on Aug. 15, 2017 and entitled "SCANNING APPARATUS
AND METHODS USEFUL FOR DETECTION OF CHEMICAL AND BIOLOGICAL
ANALYTES," the disclosures of which are incorporated herein by
reference in their entirety.
BACKGROUND
[0002] The present disclosure relates generally to detection of
chemical and biological analytes and has specific applicability to
nucleic acid sequencing.
[0003] The determination of nucleic acid sequence information is
important in biological and medical research. Sequence information
is used for identifying gene associations with diseases and
phenotypes, identifying potential drug targets, and understanding
the mechanisms of disease development and progress. Sequence
information is an important part of personalized medicine, where it
can be used to optimize the diagnosis, treatment, or prevention of
disease for a specific individual.
[0004] Many scientists and medical practitioners struggle to tap
into modern sequencing technology due to prohibitive costs to run
and maintain complex instrumentation in current commercial
offerings. These platforms favor centralized laboratories in which
expensive "factory scale" instruments are run by highly trained
specialists, and samples are batched to achieve economies of scale.
This centralized system offers very little flexibility in terms of
performance specifications users are forced into ecosystems that
are unnecessarily limited in scope and variety of use. When it
comes to clinical applications, the centralized model is costly for
doctors and their patients in terms of both the time and money
required to ship patient samples from local clinics to distant
sequencing labs. Further delays can be incurred as a centralized
sequencing lab waits to receive sufficient number of samples to
batch together into an economical run. Other applied markets such
as forensics, veterinary diagnostics, food safety, agricultural
analysis and environmental analysis suffer similar limitations.
[0005] Thus, there is a need for a sequencing platform that is
better suited for use in local laboratories in support of a
decentralized system of research and clinical care. The present
invention satisfies this need and provides related advantages as
well.
BRIEF SUMMARY
[0006] The present disclosure provides a detection apparatus that
can include (a) a vessel having a lumen and a wall, wherein the
wall has an internal surface and an external surface, wherein the
internal surface contacts the lumen; (b) a reference surface that
forms a structural loop with a detector; (c) a preload configured
to urge the external surface of the vessel to contact an area on
the reference surface; (d) a scan actuator configured to slide the
vessel along the reference surface in a scan dimension; and (e) a
transmitter configured to direct, to the detector, a signal from
the internal surface or the lumen, when the external surface of the
vessel is urged by the preload to contact the reference
surface.
[0007] Also provided is a method of scanning a vessel. The method
can include (a) translating a vessel along a reference surface of a
detection apparatus, wherein the vessel comprises a lumen and a
wall, wherein the lumen comprises analytes, wherein the reference
surface contacts at least a portion of the vessel during the
translating, and wherein the reference surface forms a structural
loop with a detector; and (b) detecting the analytes at different
locations along the vessel using the detector, wherein the vessel
is urged to the reference surface by a preload during the
detecting, thereby scanning the vessel.
[0008] In some embodiments, a method of scanning a vessel can
include (a) examining a first subset of analytes in a vessel while
applying a preload to a first portion of the vessel, wherein the
preload positions the first subset of analytes to occupy an xy
plane in a detection zone, wherein the preload is not applied to a
second portion of the vessel; (b) translating the vessel to
position a second subset of the analytes in the xy plane of the
detection zone; and (c) examining the second subset of the analytes
in the vessel while applying the preload to a second portion of the
vessel, wherein the preload positions the second subset of the
analytes to occupy the xy plane of the detection zone, wherein the
preload is not applied to the first portion of the vessel, thereby
scanning the vessel.
[0009] The present disclosure provides reactor apparatus. A reactor
apparatus can include (a) a vessel having a lumen and a wall,
wherein the wall has an internal surface and an external surface,
wherein the internal surface contacts the lumen; (b) a reference
surface that forms a structural loop with an energy source; (c) a
preload configured to urge the external surface of the vessel to
contact an area on the reference surface; (d) a scan actuator
configured to slide the vessel along the reference surface in a
scan dimension; and (e) a transmitter configured to direct energy
from the energy source to the internal surface or the lumen when
the external surface of the vessel is urged by the preload to
contact the reference surface.
[0010] Also provided is a method of performing reactions in a
vessel. The method can include (a) translating a vessel along a
reference surface of a reactor apparatus, wherein the vessel
comprises a lumen and a wall, wherein the lumen comprises
reactants, wherein the reference surface contacts at least a
portion of the vessel during the translating, and wherein the
reference surface forms a structural loop with an energy source;
and (b) directing energy from the energy source to the reactants at
different locations along the vessel, wherein the vessel is urged
to the reference surface by a preload during the directing of the
energy to the reactants, thereby performing reactions in the
vessel.
[0011] A method of performing reactions in a vessel can include (a)
delivering energy from a reactor apparatus to a first subset of
reactants in a vessel while applying a preload to a first portion
of the vessel, wherein the preload positions the first subset of
reactants to occupy an xy plane of a reaction zone, wherein the
preload is not applied to a second portion of the vessel; (b)
translating the vessel to position a second subset of the reactants
in the xy plane of the reaction zone; and (c) delivering energy
from the reactor apparatus to the second subset of the analytes in
the vessel while applying the preload to a second portion of the
vessel, wherein the preload positions the second subset of the
analytes to occupy the xy plane, wherein the preload is not applied
to the first portion of the vessel, thereby performing reactions in
the vessel.
[0012] In particular embodiments, the present disclosure provides a
detection apparatus that includes (a) a vessel having a lumen and a
wall, wherein the wall has an internal surface and an external
surface, wherein the internal surface contacts the lumen, and
wherein the external surface has length in a scan dimension x; (b)
a reference surface; (c) a preload configured to urge the external
surface of the vessel to contact an area on the reference surface,
optionally the area of contact can have a maximum length in the
scan dimension x that is shorter than length ; (d) a scan actuator
configured to slide the vessel along the reference surface in the
scan dimension x; (e) a detector; and (f) an objective configured
to direct radiation from the vessel to the detector when the
external surface of the vessel is urged by the preload to contact
the reference surface.
[0013] Also provided is a method of optically scanning a vessel.
The method can include (a) providing a vessel having a lumen and a
wall, wherein the lumen contains optically detectable analytes and
wherein the wall is transparent to the optically detectable
analytes; (b) translating a length of the vessel along a reference
surface and detecting the optically detectable analytes at
different locations along the length, wherein the reference surface
contacts only a portion of the length of the vessel at any time
during the translation, wherein the vessel is urged to the
reference surface by a preload during the detection, wherein the
detection includes transmitting radiation through the wall, then
through an objective and then to a detector, thereby optically
scanning the vessel.
[0014] The present disclosure further provides a detection
apparatus that includes (a) a vessel having a lumen and a wall,
wherein the wall has an internal surface and an external surface,
wherein the wall has a plurality of discrete contacts between the
internal surface and the external surface, wherein the internal
surface contacts the lumen, and wherein the plurality of discrete
contacts occupies a length in a scan dimension x; (b) a
transmissive surface; (c) a preload configured to urge discrete
contacts on the external surface of the vessel to contact the
transmissive surface, optionally the area of the transmissive
surface can have a maximum length in the scan dimension x that is
shorter than length ; (d) a scan actuator configured to slide the
vessel along the transmissive surface in the scan dimension x; and
(e) a detector configured to acquire signals from the discrete
contacts via the transmissive surface.
BRIEF DESCRIPTION OF THE DRAWINGS
[0015] FIG. 1 shows dimensions and axes of rotation used to
describe relative orientation of components in optical systems and
other apparatus set forth herein.
[0016] FIG. 2A shows an exploded, profile view of a flow cell and
detection apparatus; FIG. 2B shows a profile view of the flow cell
in contact with a detection apparatus; FIG. 2C shows a perspective
view of the flow cell in contact with the detection apparatus; and
FIG. 2D shows an exploded, perspective view of the flow cell in
contact with the detection apparatus.
[0017] FIG. 3A and FIG. 3B show front and rear perspective views of
a film sprocket mechanism for translating a flow cell relative to a
detection apparatus.
[0018] FIG. 4A shows a flow cell cartridge; FIG. 4B shows a film
sprocket and guide interacting with the flow cell cartridge; FIG.
4C shows a flow cell; and FIG. 4D shows a perspective view of the
film sprocket, guide, flow cell cartridge, flow cell and a motor
for the film sprocket.
[0019] FIG. 5A and FIG. 5B show front and rear perspective views of
a spur gear mechanism for translating a flow cell relative to a
detection apparatus.
[0020] FIG. 6A and FIG. 6B show front and rear perspective views of
a ball screw mechanism for translating a flow cell relative to a
detection apparatus.
[0021] FIG. 7A shows a perspective view of a heating plate and film
sprocket scanning mechanism and FIG. 7B shows a perspective view of
an objective and the heating plate and film sprocket scanning
mechanism.
[0022] FIG. 8A shows a perspective view of a fluidic caddy with an
attached flow cell; FIG. 8B shows an expanded view of the
attachment points for the flow cell to the caddy; FIG. 8C shows a
front view of the fluidic caddy with attached flow cell; FIG. 8D
shows a side view of the fluidic caddy with attached flow cell;
FIG. 8E shows a top view of the fluidic caddy with attached flow
cell; and FIG. 8F shows a perspective view of the fluidic caddy
emptied of several fluidic components.
[0023] FIG. 9A shows a perspective view of a fluidic caddy and flow
cell interacting with a detection apparatus; FIG. 9B shows a top
view of the fluidic caddy and flow cell interacting with the
detection apparatus; and FIG. 9C shows a perspective view of the
fluidic caddy disengaged from the detection apparatus.
[0024] FIG. 10A shows a side view, and expanded view of section c,
for a fluidic caddy with attached flow cell; FIG. 10B shows the
expanded view of the flow cell after being released from the
fluidic caddy; FIG. 10C shows a top view of a fluidic caddy engaged
with components of a detection apparatus; FIG. 10D shows a cutaway
view of the fluidic caddy (along line m) engaged with components of
a detection apparatus; and FIG. 10E shows an expanded view of the
fluidic caddy engaged with components of a detection apparatus.
[0025] FIG. 11 shows a cutaway profile view of a rigid support
aligned to a flow cell and an immersion objective.
DETAILED DESCRIPTION
[0026] The present disclosure provides apparatus and methods for
detecting analytes, such as chemical or biological analytes. The
detection can occur for analytes that are consumed, modified or
produced as part of a reaction of interest. Several embodiments of
the apparatus and methods are well suited to detection of
repetitive reactions such as those used to characterize or
synthesize polymers. A wide variety of polymers exist in nature and
an infinite variety of polymers can be made by natural processes,
or synthetic processes that nevertheless utilize a relatively small
number of monomeric building blocks. For example, DNA is
synthesized in nature from four different nucleotides, as is RNA.
Protein, another ubiquitous polymer, is made from 20 different
genetically encoded amino acids. Apparatus and methods of the
present disclosure can be configured to sequentially detect
monomeric building blocks, thereby providing a capability to
identify any sequence. In particular embodiments, the apparatus and
methods can be configured to detect analytes that are consumed,
produced or modified during a multi-cycle, repetitive reaction
process. For example, intermediate products can be detected at each
individual cycle. By way of more specific example, nucleic acids
can be sequenced by serially delivering reagents that specifically
react with, or bind to, the four different types of nucleotide
monomers, and components of each reaction (e.g. labeled nucleotides
or labeled polymerases) can be detected during or after each cycle.
Alternatively, nucleic acids can be synthesized by serially
delivering one of four different nucleotide monomers, or precursors
thereof, in a predefined order to a growing polymer and then
products (e.g. blocking moieties released during deprotection) can
be detected for each cycle. Sequencing or synthesis of proteins can
also be detected cyclically using apparatus and methods set forth
herein.
[0027] Various aspects of the present invention are exemplified
with regard to scanning detection. It will be understood that
apparatus and methods set forth herein can be used for precise
spatially resolved manipulation of reagents or substrates in a
vessel whether or not the reagents or substrates are detected. For
example, light energy can be delivered to a vessel to perform
photoreactions at spatially resolved locations in a vessel or to
fabricate light responsive materials in a spatially resolved
manner.
[0028] This disclosure provides apparatus and methods that can be
used to observe a vessel by translational movement of the vessel
relative to a detector. Also provided are apparatus and methods to
address a vessel, for example, by delivery of localized energy, by
translational movement of the vessel relative to an energy source.
When detecting analytes, this scanning motion allows the detector
to collect signals from sequential subsections of the vessel. The
collective combination of signals sums to a total field of
detection that is larger than the static detection field of the
detector. Taking, for example, a vessel having an interior surface
to which an array of optically labeled analytes is attached,
translation of the vessel relative to an optical detector can
provide an image of the array that is larger than the field of view
of the detector. Similarly, scanning-based delivery of energy can
allow sequential reactions to be carried out in a vessel.
[0029] A difficulty that plagues many scanning detectors is that
mechanisms for translating the vessel relative to the detector are
coupled with mechanisms for adjusting rotational registration of
the vessel with respect to the detector. As such, the scanning
detector is burdened with a tolerance stack that includes not only
translational tolerances but also rotational tolerances. Relatively
small amounts of rolling rotation or pitching rotation (i.e.
rotation around the x axis and rotation around they axis,
respectively, as diagrammed in FIG. 1) can have significant adverse
impacts on high resolution imaging of an analyte array. This
adverse impact is exacerbated in optical scanning applications
since a small pitch deviation (i.e. rotation around they axis) will
manifest as an increasing drift out of focus as the optical
detector scans a vessel along the x dimension. The longer the scan,
the further the deviation from focus.
[0030] A common solution to the problem of high tolerance stacks in
optical scanners has been to employ moving stages having high
precision actuators that are adjustable in a variety of
translational and rotational directions. High precision actuators
add cost and complexity to a scanner, and such rigs typically
require highly trained technicians for routine maintenance.
Particular embodiments of the apparatus and methods set forth
herein avoid these problems by decoupling the mechanism that is
used to translate a vessel with respect to a detector from the
mechanism that is used to rotationally register the vessel with
respect to the detector. Decoupling translation from rotational
registration reduces the tolerance stack for the translation
mechanism in detection apparatus and other apparatus of the present
disclosure.
[0031] A further advantage of replacing a typical stage with a
vessel translation apparatus of the present disclosure is that the
vessel can be scanned more quickly. The increase in scanning speed
is, in large part, a function of the vessel translation apparatus
being configured to move a mass that is smaller than a typical
stage. A small mass takes less time to settle compared to a larger
mass that is moved the same distance. For example, the time spent
waiting for a vessel to settle prior to acquiring an image becomes
increasingly significant as the desired resolution for detection
increases because the motion of the vessel must dampen to a point
that the average displacement experienced by features of the object
under observation is small enough to preclude substantial
distortions in the image. Taking as an example a typical nucleic
acid sequencing apparatus, DNA is present in sites of an array that
are only a few microns apart and that are observed at low micron
resolution. A typical stage used to move the array for sequencing
requires settle times of several hundred milliseconds to dampen to
the point that displacements are less than a few microns. Avoiding
a typical stage by using an apparatus of the present disclosure
allows settle times on the order of a few tens of milliseconds. The
milliseconds can add up to hours for a nucleic sequencing protocol
or other repetitive scanning operation. For example, saving 500
hundred milliseconds per image adds up to a savings of about 4
hours in settling time alone for a sequencing protocol that
acquires 200 images per cycle and performs 150 cycles per run.
Similar improvements in processing speed can be achieved for other
scanning applications such as photochemistry, photolithography,
microfabrication or nanofabrication (e.g. via laser etching), laser
ablation or the like.
[0032] Although apparatus and methods set forth herein provide
advantages in reducing settle time, it will be understood that the
uses need not be limited to processes that include a settling step.
Accordingly, apparatus and methods set forth herein in the context
of so called "step and shoot" scanning procedures can be applied to
continuous scanning operations such as time delayed integration
(TDI) scanning. For example, apparatus and methods set forth herein
can be modified for use in TDI line scanning operations such as
those set forth in U.S. Pat. No. 7,329,860, which is incorporated
herein by reference.
[0033] As set forth in further detail herein, rotational
registration of a vessel with respect to a detector can be achieved
by physically contacting the vessel with a reference surface, the
reference surface being rotationally fixed with respect to the
detector. In particular embodiments, as exemplified below, a vessel
can be compressed to the reference surface by a preload.
Separately, translation can be achieved by a scan actuator (e.g. a
gear) that interacts directly with another surface of the vessel
(e.g. a rail that complements the gear). The preload and scan
actuator need not interact to achieve motion and registration of
the vessel. For example, the preload need not be applied to the
vessel while the vessel is being translated. However, interaction
between the preload and scan actuator can occur for certain
applications of the apparatus and methods set forth herein.
Accordingly, the preload can be applied to the vessel while the
vessel is being translated.
[0034] In some embodiments, a vessel that is to be detected can be
a component of a cartridge. The cartridge can provide a convenient
mechanism to deliver the vessel to a detector. For example, a
detector can be maintained inside of an analytical instrument to
protect the detector from environmental factors such as moisture,
dust or light. A cartridge can be introduced to the analytical
instrument via a door or opening such that the vessel is contacted
with the detector. In some embodiments, the analytical instrument
will remove the vessel from the cartridge and translate the vessel
past the detector in a way that does not necessarily involve
movement of the cartridge. Alternatively, the vessel can maintain
contact with the cartridge such that both the cartridge and vessel
are moved to achieve translation or scanning. In a further
alternative, the cartridge can be a component of the analytical
instrument and the vessel can be introduced to the instrument by
placing the vessel into the cartridge.
[0035] Alternatively and/or additionally, the vessel can be a
component of a caddy that also includes reservoirs and fluidic
components that deliver reagents to the vessel during the course of
a reaction that is detected, such as a nucleic acid sequencing
reaction. In some embodiments, the caddy includes sufficient
fluidic components that it functions as a "wet" component and the
analytical instrument housing the detector functions as a "dry"
component. An advantage of having separate wet and dry components
is that the caddy and vessel can be dedicated to a particular
sample or reaction, and when the reaction is complete, the caddy
and vessel can be removed from the analytical instrument and
replaced with a new caddy and vessel dedicated to a second sample
or reaction. Because the samples, reagents and reaction products
for each of these two reactions are physically separated from the
analytical instrument, cross contamination between the reactions,
that would otherwise cause detection artifacts, are avoided.
[0036] The physical separation of the components provides a further
advantage of avoiding unnecessary downtime for the analytical
instrument if the fluidic component experiences mechanical
difficulties. Specifically, unlike many commercially available
analytical instruments which have permanently integrated fluidics,
a fluidic system failure can be conveniently overcome by merely
removing a faulty fluidic caddy and replacing it with another so
that the analytical instrument experiences little to no downtime.
In some embodiments, the caddy is disposable, for example, being
made from relatively inexpensive components. The caddy can be
configured in a way that reagents are sealed in the caddy thereby
avoiding unwanted contamination of the environment and unwanted
exposure of laboratory personnel and equipment to the reagents.
Alternatively, the fluidics caddy can be emptied, refilled and
re-used if desired for a particular application.
[0037] In some embodiments, a fluidic caddy of the present
disclosure includes not only reagent reservoirs, but also includes
one or more waste reservoirs. Reagent that is not consumed in a
reaction and/or unwanted products of a reaction can be collected in
the waste reservoir. Advantages of retaining pre- and post-reaction
fluids in a caddy include convenience of the user in handling a
single fluidic component before and after a reaction is performed,
minimizing user contact with chemical reagents, providing a compact
footprint for the apparatus and avoiding unnecessary proliferation
of fluid containers.
[0038] Exemplary fluidic caddies, reaction vessels and fluidic
components that can be modified, in accordance with teachings
herein, for use in combination with detection components of the
present disclosure are described in commonly owned U.S. patent
application Ser. No. 15/922,661, which claims the benefit of U.S.
Provisional App. No. 62/481,289, each of which is incorporated
herein by reference. Other fluidic components that are useful,
particularly for cyclic reactions such as nucleic acid sequencing
reactions, are set forth in US Pat. App. Pub. Nos. 2009/0026082 A1;
2009/0127589 A1; 2010/0111768 A1; 2010/0137143 A1; or 2010/0282617
A1; or U.S. Pat. Nos. 7,329,860; 8,951,781 or 9,193,996, each of
which is incorporated herein by reference.
[0039] The details of one or more embodiments are set forth in the
accompanying drawings and the description below. The drawings and
description are provided as examples for purposes of explanation
and are not necessarily intended to limit the scope of the
invention. The invention is susceptible to modifications in the
methods and materials, as well as alterations in the fabrication
methods and equipment. Such modifications will become apparent to
those skilled in the art from a consideration of the drawings and
the description below.
[0040] The present disclosure provides a detection apparatus. The
apparatus can include (a) a vessel having a lumen and a wall,
wherein the wall has an internal surface and an external surface,
wherein the internal surface contacts the lumen; (b) a reference
surface that forms a structural loop with a detector; (c) a preload
configured to urge the external surface of the vessel to contact an
area on the reference surface; (d) a scan actuator configured to
slide the vessel along the reference surface in a scan dimension;
and (e) a transmitter configured to direct, to the detector, a
signal from the internal surface or the lumen, when the external
surface of the vessel is urged by the preload to contact the
reference surface.
[0041] In particular embodiments, a detection apparatus can include
(a) a vessel having a lumen and a wall, wherein the wall has an
internal surface and an external surface, wherein the internal
surface contacts the lumen, and wherein the external surface has
length in a scan dimension x; (b) a reference surface; (c) a
preload configured to urge the external surface of the vessel to
contact an area on the reference surface, optionally the area of
contact can have a maximum length in the scan dimension x that is
shorter than length ; (d) a scan actuator configured to slide the
vessel along the reference surface in the scan dimension x; (e) a
detector; and (f) an objective configured to direct radiation from
the vessel to the detector when the external surface of the vessel
is urged by the preload to contact the reference surface.
[0042] The present disclosure also provides is a method of scanning
a vessel. The method can include (a) translating a vessel along a
reference surface of a detection apparatus, wherein the vessel
comprises a lumen and a wall, wherein the lumen comprises analytes,
wherein the reference surface contacts at least a portion of the
vessel during the translating, and wherein the reference surface
forms a structural loop with a detector; and (b) detecting the
analytes at different locations along the vessel using the
detector, wherein the vessel is urged to the reference surface by a
preload during the detecting, thereby scanning the vessel.
[0043] In some embodiments, a method of scanning a vessel can
include (a) examining a first subset of analytes in a vessel while
applying a preload to a first portion of the vessel, wherein the
preload positions the first subset of analytes to occupy an xy
plane in a detection zone, wherein the preload is not applied to a
second portion of the vessel; (b) translating the vessel to
position a second subset of the analytes in the xy plane of the
detection zone; and (c) examining the second subset of the analytes
in the vessel while applying the preload to a second portion of the
vessel, wherein the preload positions the second subset of the
analytes to occupy the xy plane of the detection zone, wherein the
preload is not applied to the first portion of the vessel, thereby
scanning the vessel.
[0044] Also provided is a method of optically scanning a vessel.
The method can include (a) providing a vessel having a lumen and a
wall, wherein the lumen contains optically detectable analytes and
wherein the wall is transparent to the optically detectable
analytes; (b) translating a length of the vessel along a reference
surface and detecting the optically detectable analytes at
different locations along the length, wherein the reference surface
contacts only a portion of the length of the vessel at any time
during the translation, wherein the vessel is urged to the
reference surface by a preload during the detection, wherein the
detection includes transmitting radiation through the wall, then
through an objective and then to a detector, thereby optically
scanning the vessel.
[0045] FIG. 2 shows an exemplary arrangement for scanning a vessel
relative to a detector. As shown in the profile views of FIG. 2A
and FIG. 2B, the vessel is a flow cell 101 that is aligned with
objective 110 via a rigid body 100. The back side of rigid body 100
has a conical depression 116 that complements the shape of
objective 110. Accordingly, objective 110 can be moved close to the
flow cell for a desired focus or resolution. Any of a variety of
depression shapes can be used as desired to accommodate the shapes
for various objectives or other optical components. The front side
of rigid body 100 has a reference surface 117 that will contact a
planar face of flow cell 101. The flow cell 101 is maintained in
contact with the reference surface 117 by a preload that applies
positive pressure to the side of flow cell 101 that is opposite the
reference surface 117. The preload is formed by compression foot
102 which contacts flow cell 101 under force of spring 103.
[0046] Generally, reference surface 117 and compression foot 102
create low friction contacts with flow cell 101. This allows the
flow cell to slide past the reference surface 117 and to slide past
compression foot 102 while under compression force of the preload.
This compression provides alignment of the flow cell 101 with the
objective 110 via the rigid body throughout the course of flow cell
101 scanning by the objective 110. The reference surface and
objective are components of a structural loop. The structural loop
contains structural elements that locate the vessel (e.g. flow
cell) with respect to the detector (e.g. via the objective).
Because the reference surface is pre-aligned with the objective,
compressing the flow cell to the reference surface prevents
unwanted pitch and roll of the flow cell with respect to the
objective. Components of FIG. 2 that are in the structural loop
include reference surface 117, which is connected to rigid body
100, which is connected to base 114. Base 114 can be connected to a
plate or other structural element that is physically connected to
components of an optical system such as those exemplified in FIG.
9.
[0047] In the example shown in FIG. 2, reference surface 117 is
polished aluminum, which provides rigidity for aligning the flow
cell 101 to the objective 110 and a low friction surface for
sliding the glass surface of the flow cell 101. Any of a variety of
materials can be used that provide rigidity and low friction for
the reference surface including, for example, acetal resins (e.g.
Delrin.RTM. available from DuPont, Wilmington, Del.), diamond like
carbon or polished metals. The compression foot 102 provides a low
friction surface for the sliding translation of the flow cell 101
glass surface and also provides compressibility to form a compliant
contact with the flow cell 101 under the force of spring 103. Any
of a variety of materials can be used that provide low friction to
the compression foot including, for example, those set forth above
for reference surface 117. Optionally, a low friction material used
in an apparatus herein can also be compressible, examples of which
include, but are not limited to, polytetrafluoroethylene (PTFE,
Teflon.RTM.), perfluoroalkoxy alkane (PFA), fluorinated ethylene
propylene (FEP), silicone foam, nitrile rubber, Buna-N, Perbunan,
acrylonitrile butadiene rubber or nitrile butadiene rubber (NBR).
Alternatively or additionally, low friction can be achieved using
ball bearings, rollers and/or lubricating fluids. Typically, the
lubricating fluid is used on the side of the flow cell that is not
between the analytes and detector or a fluid is used that does not
interfere with detection. In some embodiments, lubricating fluids
are not present at the interface between the reference surface and
the exterior surface of the vessel wall. For example, lubricating
fluids can be avoided to prevent interference caused when the fluid
enters the area between the detector and vessel.
[0048] In particular embodiments, a vessel (or cartridge containing
a vessel) is positioned in an xy plane without contacting a
reference surface. For example, a vessel (or cartridge) can be
urged, by a preload, toward a fluid bearing or magnetic bearing
such that the combination of forces provided by the preload and
bearing results in a desired positioning. A fluid bearing can be a
gas bearing, whereby gas pressure provides a force for positioning
the vessel (or cartridge). Another useful type of fluid bearing is
a liquid bearing, whereby liquid pressure provides a force for
positioning the vessel (or cartridge). The liquid can be selected
for the ability to index match with optical components of the
system, such as the wall of the vessel, so as to minimize
aberrations when detecting optical signals or delivering
radiation.
[0049] As shown in FIG. 2C and FIG. 2D, reference surface 117 has a
planar surface that forms a flat ring on the front face of rigid
body 100. The ring is raised compared to the front face of rigid
body 100. Raising the reference surface helps to prevent unwanted
contact between the flow cell 101 and rigid body 100 that may
otherwise create friction that hinders translation. Raising the
reference surface 117 also isolates the area of the flow cell that
is to be detected and prevents unwanted warping that could
otherwise occur if the flow cell contacted other regions of rigid
body 101. In the example of FIG. 2, the reference surface has an
area that is smaller than the surface of the flow cell and thus
only contacts a portion of the flow cell surface. However, in
alternative embodiments, the reference surface can be substantially
the same size or larger than the flow cell surface and thus can
contact substantially all of the flow cell surface (optionally,
excepting the area of the flow cell surface that is juxtaposed with
a detection window, objective or other transmitter).
[0050] In the example shown, reference surface 117 surrounds
circular window 118, this window being a hole through rigid body
100. Alternatively, circular window 118 can include a material that
is capable of transmitting a signal that is to be detected. For
example, the window can be made of quartz, glass, or plastic that
facilitates transmission of signals that are to be detected. In
some configurations, the window can contain an index matched
immersion fluid that contacts the flow cell surface to facilitate
detection, as set forth in further detail below with regard to FIG.
11. The circular window 118 is aligned with the front lens 115 of
the objective 110 such that the objective 110 can observe flow cell
101 through the window 118. Compression foot 102 has a flat ring
shape providing a footprint on flow cell 101 that is complementary
to the footprint of flat ring 117 on the opposite side of the flow
cell. In this example, the preload (via foot 102) has a contact
area with the vessel (flow cell 101) that is the same as the area
of contact between reference surface 117 and the vessel.
Alternatively, the preload can have a contact area with the vessel
that is smaller than the area of contact between the reference
surface and the vessel. Indeed, the preload can have a contact area
with the vessel that is no larger than the area of contact between
the reference surface and the vessel.
[0051] Generally, complementarity between the footprints of the
preload and reference surface can be configured to result in the
compression foot 102 having a contact area on the flow cell 101
that excludes surface area of the flow cell opposite the circular
window 118 and that further excludes surface area of the flow cell
opposite the region of the rigid body that surrounds reference
surface 117. Complementarity between the footprints of compression
foot 102 and reference surface 117 helps to maintain flatness for
the portion of the flow cell surface that is observed through
window 118. This complementarity can be beneficial for detecting
analytes on the inner surface of the flow cell, especially at high
magnification and high resolution. The complementarity can also
facilitate trans-illumination, whereby radiation can pass back or
forth through a path defined by the hollow space in the spring 103,
compression foot 102 and window 118. The circular shape of the
reference surface and preload is exemplary. Other shapes can be
used including, but not limited to, square, rectangular,
polyhedral, elliptical, triangular or the like. Moreover, the shape
need not be continuous. Instead the reference surface and/or
contact surface for the preload can be a discontinuous area such as
that formed by two parallel tracks or by interruptions to the above
shapes. Particularly useful applications are nucleic acid
microarray detection and nucleic acid sequencing. The shapes and
orientations for preload and reference surface can be used for
apparatus that deliver energy to a vessel or that detect
non-optical signals.
[0052] As exemplified by FIG. 2, a particularly useful vessel for
use in a detection apparatus or other apparatus of the present
disclosure is a flow cell. Any of a variety of flow cells can be
used including, for example, those that include at least one
channel and openings at either end of the channel. The openings can
be connected to fluidic components to allow reagents to flow
through the channel. The flow cell is generally configured to allow
detection of analytes within the channel, for example, in the lumen
of the channel or on the inner surface of a wall that forms the
channel. In some embodiments, the flow cell can include a plurality
of channels each having openings at their ends. For example, the
flow cell shown in FIG. 2 has three channels 120, 121 and 122 each
having openings at both ends. Multiple channels can interact with a
fluidic system via a manifold.
[0053] In particular embodiments, a flow cell will include a solid
support to which one or more target analytes or reagents are
attached. A particularly useful solid support is one having an
array of sites. Arrays provide the advantage of facilitating
multiplex detection. For example, different reagents or analytes
(e.g. cells, nucleic acids, proteins, candidate small molecule
therapeutics etc.) can be attached to an array via linkage of each
different analyte to a particular site of the array. Exemplary
array substrates that can be useful include, without limitation, a
BeadChip.TM. Array available from Illumina, Inc. (San Diego,
Calif.) or arrays such as those described in U.S. Pat. Nos.
6,266,459; 6,355,431; 6,770,441; 6,859,570; or 7,622,294; or PCT
Publication No. WO 00/63437, each of which is incorporated herein
by reference. Further examples of commercially available array
substrates that can be used include, for example, an Affymetrix
GeneChip.TM. array. A spotted array substrate can also be used
according to some embodiments. An exemplary spotted array is a
CodeLink.TM. Array available from Amersham Biosciences. Another
array that is useful is one that is manufactured using inkjet
printing methods such as SurePrint.TM. Technology available from
Agilent Technologies.
[0054] Other useful array substrates include those that are used in
nucleic acid sequencing applications. For example, arrays that are
used to create attached amplicons of genomic fragments (often
referred to as clusters) can be particularly useful. Examples of
substrates that can be modified for use herein include those
described in Bentley et al., Nature 456:53-59 (2008), PCT Pub. Nos.
WO 91/06678; WO 04/018497 or WO 07/123744; U.S. Pat. Nos.
7,057,026; 7,211,414; 7,315,019; 7,329,492 or 7,405,281; or U.S.
Pat. App. Pub. No. 2008/0108082, each of which is incorporated
herein by reference.
[0055] An array can have sites that are separated by less than 100
.mu.m, 50 .mu.m, 10 .mu.m, 5 .mu.m, 1 .mu.m, or 0.5 .mu.m. In
particular embodiments, sites of an array can each have an area
that is larger than about 100 nm.sup.2, 250 nm.sup.2, 500 nm.sup.2,
1 .mu.m.sup.2, 2.5 .mu.m.sup.2, 5 .mu.m.sup.2, 10 .mu.m.sup.2, 100
.mu.m.sup.2, or 500 .mu.m.sup.2. Alternatively or additionally,
sites of an array can each have an area that is smaller than about
1 mm.sup.2, 500 .mu.m.sup.2, 100 .mu.m.sup.2, 25 .mu.m.sup.2, 10
.mu.m.sup.2, 5 .mu.m.sup.2, 1 .mu.m.sup.2, 500 nm.sup.2, or 100
nm.sup.2. Indeed, a site can have a size that is in a range between
an upper and lower limit selected from those exemplified above. An
array can have sites at any of a variety of densities including,
for example, at least about 10 sites/cm.sup.2, 100 sites/cm.sup.2,
500 sites/cm.sup.2, 1,000 sites/cm.sup.2, 5,000 sites/cm.sup.2,
10,000 sites/cm.sup.2, 50,000 sites/cm.sup.2, 100,000
sites/cm.sup.2, 1,000,000 sites/cm.sup.2, 5,000,000 sites/cm.sup.2,
or higher. An embodiment of the apparatus or methods set forth
herein can be used to image an array at a resolution sufficient to
distinguish sites at the above densities or site separations.
[0056] Several embodiments utilize optical detection of analytes in
a flow cell. Accordingly, a flow cell can include one or more
channels each having at least one transparent window. In particular
embodiments, the window can be transparent to radiation in a
particular spectral range including, but not limited to x-ray,
ultraviolet (UV), visible (VIS), infrared (IR), microwave and/or
radio wave radiation. In some cases, analytes are attached to an
inner surface of the window(s). Alternatively or additionally, one
or more windows can provide a view to an internal substrate to
which analytes are attached. Exemplary flow cells and physical
features of flow cells that can be useful in a method or apparatus
set forth herein are described, for example, in US Pat. App. Pub.
No. 2010/0111768 A1, WO 05/065814 or US Pat. App. Pub. No.
2012/0270305 A1, each of which is incorporated herein by reference
in its entirety.
[0057] Several examples herein are demonstrated for a rectangular
flow cell 101 having elongated channels. In these examples, the
area of contact between the flow cell 101 and reference surface 117
has a maximum length in the scan dimension x that is shorter than
the length of the flow cell lane in scan dimension x. More
specifically, the diameter of ring 117 is shorter than the length
of lanes 120, 121 or 122. Alternatively or additionally, the area
of contact between the flow cell 101 and reference surface 117 can
have a maximum width w in dimension y that is shorter than the
width of the flow cell lane in dimension y. Specifically, the
diameter of ring 117 can be shorter than the width of any one of
lanes 120, 121 or 122.
[0058] Similarly, the maximum diameter or length of window 118 in
the scan dimension x can be shorter than the length of the flow
cell lane in the scan dimension x. Alternatively or additionally,
the maximum diameter or width of window 118 in the y dimension can
be shorter than the width of any one of lanes 120, 121 or 122. In
this configuration, the complete width of the lane can be observed
by translation in they direction. In some embodiments, the area of
window 118 and width of the lane can be configured so that
translation in they dimension is not necessary to observe the
entire width of the lane. For example, the area of window 118 can
have a maximum diameter or width w in dimension y that is
equivalent to or longer than the width of the flow cell lane in
dimension y.
[0059] In particular embodiments a vessel, such as a flow cell, can
be moved in an arcuate path during all or part of a scanning
operation. Looking to the flow cell orientation in FIG. 1, the
arcuate path can result from rotation around the yaw axis. The
arcuate path can be a circle, spiral or other path that is
desirable for scanning a vessel. Optionally, the area of contact
between a vessel and reference surface can have a length or area
that is smaller than the length or area, respectively, of the
arcuate path. By way of more specific example, a ring-shaped
reference surface can have a diameter that is shorter than the
length of the arcuate path or shorter than the length of a lane in
a flow cell that is moved along the arcuate path. Similarly, the
maximum diameter or area of a window in the reference surface,
through which detection occurs, can be smaller than the length or
area, respectively, of the arcuate path; or the window can be
smaller than a flow cell lane that is scanned along an arcuate
path.
[0060] A flow cell need not be rectangular in shape. Alternative
shapes that can be used include, but are not limited to, a disc,
square, polygon or irregular shape. The lanes of a flow cell can
follow a linear path, arcuate path, winding path or the like. Other
types of vessels can also be used. For example, a well of a
multi-well strip or multi-well plate can be detected using an
apparatus or method of the present disclosure. The bottom surface
of a well can be urged toward a reference surface by a preload
applied to the top of the vessel (e.g. by contacting a compression
foot to the upper side of a multi-well plate or multi-well strip).
Optionally, the well can have a flat bottom that contacts the
reference surface. As a further option, the well will be larger
than the field of view of the detector. For example, the well may
be circular in shape and may have a diameter in scan dimension x
that is longer than the length of the reference surface in the scan
dimension x.
[0061] Another exemplary vessel type is a cylindrical- or
tube-shaped vessel such as a capillary tube. The body of a tube can
be held to a reference surface under the force of a preload as
exemplified herein for flat shaped vessels. In an exemplary
configuration the length of the tube can be parallel to the scan
axis such that scanning the tube along x will result in relative
motion of the reference surface along the length of the tube. For a
tube that is configured in this orientation, it may also be useful
to rotate the tube in the roll axis. This rotation will result in
relative motion of the reference surface around the circumference
of a section of the tube. Combining translation along x and
rotation along the roll axis can allow a substantial surface area
of the tube to come into contact with the reference surface. For
example, the tube and reference surface can move in a helical or
spiral path relative to each other. The reference surface can be
flat, as exemplified herein for flow cells having a flat exterior
wall. Alternatively, the reference surface can have a curved shape
(e.g. u-shaped or saddle-shaped cross section) that accommodates
and orients a cylindrical- or tube-shaped vessel that it
contacts.
[0062] Typically, the vessel wall is made from a rigid material
that is not readily flexible under the conditions used. In
alternative embodiments, a vessel is made from a flexible material,
for example, forming a sheet, tape, belt or ribbon that can be
passed along a reference surface and detected while the vessel is
under the urging of a preload. For example, a plurality of
analytes, such as an array of nucleic acids, can be attached to the
surface of the flexible material and detected when in contact with
the reference surface. Exemplary, flexible materials having
attached analytes are described, for example, in U.S. Pat. No.
9,073,033 and US Pat. App. Pub. No. 2016/0076025 A1, each of which
is incorporated herein by reference.
[0063] When using a vessel having a flexible wall, it may be
advantageous to pull the wall material over a reference surface,
for example, to stretch or straighten the portion of the wall
material that is observed by a detector. For example, the reference
surface can be a raised rim that surrounds a detection window and
the flexible material can be pulled over the rim to apply a pulling
force across the window. Pulling can be achieved for example by
applying suction to the flexible material via a vacuum chuck that
surrounds the raised rim. Suction can be applied as an alternative
or supplement to other preload mechanisms set forth herein.
[0064] As will be evident from the examples set forth herein, a
vessel can be open (e.g. a well of a multi-well plate, surface of a
chip, or surface of a sheet) or the vessel can be enclosed (e.g. a
lane of a flow cell). It will be understood that, wells of a
multi-well plate can optionally be covered to create an enclosed
vessel and similarly a sheet, belt, tape or ribbon can have
multiple layers such that an internal lumen occurs between layers.
Alternatively, a vessel can have one or more open structures such
as a trough, well or other concave structure that contains a fluid.
A vessel can also have a convex or protruding structure such as a
post or ridge, and optionally individual protrusions can each be
attached to one or more analyte that is to be detected or
manipulated.
[0065] The preload exemplified in FIG. 2 creates a pushing force on
the side of the vessel (e.g. flow cell) that is opposite the side
of the vessel that contacts the reference surface. Pushing force
can derive from a spring, clamp, positive air pressure, positive
fluid pressure, charge repulsion, charge attraction, magnetic
attraction or magnetic repulsion. Alternatively, a preload can be
configured to create a pulling force on the vessel. For example, a
magnetic or ferromagnetic material that is in or on the vessel can
be attracted to the reference surface, or charges in or on the
vessel can be attracted to the reference surface. In this example,
the reference surface or area surrounding the reference surface can
contain magnetic or ferromagnetic material that acts as a preload.
In another embodiment, pulling force can result from a vacuum chuck
that is configured to apply suction to an area of the vessel that
contacts the reference surface. In a further embodiment, a magnetic
clamping force can be used, whereby the vessel is sandwiched
between a magnetic or ferromagnetic material on or around the
reference surface that attracts a magnetic or ferromagnetic body
that is external to the opposite side of the vessel.
[0066] A detection apparatus or other apparatus of the present
disclosure can include a scan actuator that is configured to slide
a vessel along a reference surface. The vessel can slide along the
reference surface and along the surface of the preload. Generally,
the scan actuator is configured to move the vessel while the vessel
is in contact with the reference surface under the urging of a
preload. However, it is also possible to translate the vessel
without simultaneously applying a preload to the vessel. It is also
possible to translate the vessel through a space defined by a
bearing that does not physically contact the vessel, such as a
fluid bearing or magnetic bearing. For example, a vessel can be
positioned via opposing forces of a preload against a bearing.
Particularly useful actuators employ one or more gears that
interact with perforations or threads on a flow cell or on a
cartridge that contains the flow cell. Several examples are set
forth below.
[0067] In some embodiments, the scan actuator can use a film
sprocket mechanism. The vessel that is to be translated, or a
cartridge that holds the vessel, can contain a track of
perforations that engages a sprocket in a detection apparatus to
achieve translation. As shown in the exemplary configuration of
FIG. 3, flow cell 101 is housed in cartridge 125, which contains
two perforation tracks 130 and 140. Perforation track 130 is
located near the top edge of the cartridge 125 and runs parallel to
the longest dimension of the flow cell. Perforation track 140 is
located near the opposite edge of the cartridge 125 and also runs
parallel to . Sprockets 150 and 160 are configured to engage
perforation tracks 130 and 140, respectively, when urged toward
reference surface 117 by the force of preload spring 103. The flow
cell 101 can be translated in scan dimension x, which is parallel
to , by rotating the engaged sprockets 150 and 160.
[0068] FIG. 4A shows a cartridge 400 having an inset 403 for flow
cell 430. The inset includes notches 404 and 405 that are placed to
facilitate adjustment or removal of the flow cell 430. Cartridge
400 has a single perforation track 401 near the top edge 402. As
shown in FIG. 4B, the perforations are complementary to teeth on
sprocket 420 and perforation track 401 is inset into the face of
cartridge 400 thereby providing a track that engages guide 410.
Guide 410 slots into perforation track 401 to prevent rotation of
cartridge 400 in the yaw axis during translation under the action
of sprocket 420, thereby preventing unwanted yaw rotation of the
flow cell 430 relative to a detector. As shown in FIG. 4C, flow
cell 430 includes a bottom plate 431 that is sized for pressure fit
with inset 403 and also includes a top plate 440. A channel 443 is
formed between plates 431 and 440 due to presence of a spacer or
gasket. The top plate 440 also includes holes 441 and 442 which act
as inlet and outlet for channel 443. A perspective view of the
cartridge 400 with assembled flow cell 430, sprocket 420 with motor
425, and guide 410 is shown in FIG. 4D.
[0069] Another useful mechanism for scan actuation is a spur gear
that engages teeth on an edge of a flow cell, or on an edge of a
cartridge holding the flow cell. FIG. 5A shows cartridge 200 which
is pressure fitted to flow cell 101, and which has a serrated
bottom edge 240 and smooth top edge 241. Serrated bottom edge 240
engages spur gear 230 when cartridge 200 is urged by preload spring
103 to contact a reference surface on rigid body 100. The cartridge
200 and flow cell 101 are translated by rotating spur gear 230.
Wheel guides 210 and 220 engage the smooth edge 241 of the
cartridge 200, when the cartridge 200 is positioned to contact the
flow cell 101 with a reference surface on rigid body 100. The wheel
guides function to prevent rotation of the cartridge 200 and flow
cell 101 about the yaw axis.
[0070] Scan actuation can also employ a ball screw that engages a
threaded catch on a flow cell, or on a cartridge holding the flow
cell. FIG. 6A shows cartridge 300 which is pressure fitted to flow
cell 101, and which has a threaded catch 311 on the top and two
guide catches 312 and 313 on the bottom. Threaded catch 311 engages
screw 310 when cartridge 300 is urged by preload spring 103 to
contact a reference surface on rigid body 100. The cartridge 300
and flow cell 101 are translated by rotating screw 310 against
threads of catch 311. Guide catches 312 and 313 engage rail 320,
when the cartridge 300 is positioned to contact the flow cell 101
with reference surface 117. The guide catches 312 and 313 function
to prevent rotation of the cartridge 300 and flow cell 101 about
the yaw axis.
[0071] Scan actuation can use mechanical contact between the motor
and vessel (or vessel cartridge) as exemplified above.
Alternatively or additionally, interaction between motor and vessel
(or vessel cartridge) can be mediated by magnetic attraction. For
example, the vessel or cartridge can have a magnetic or
ferromagnetic material that interacts with a magnetic or
ferromagnetic component of the actuator.
[0072] Whether using mechanical contact or other interactions to
mediate actuation, a linear motor can be used to drive the scanning
motion. Exemplary linear motors that can be used include
synchronous linear motors, induction linear motors, homopolar
linear motors and piezo electric linear motors.
[0073] An apparatus of the present disclosure can further include a
y actuator configured to change the relative translational position
of the detector and the vessel along they dimension. Taking as an
example the apparatus shown in FIG. 2, a y actuator can operate,
for example, by changing the relative translational position of the
objective 110 and the reference surface 117. Alternatively or
additionally, a y actuator can operate by changing the relative
translational position of the flow cell 101 and the reference
surface 117. Translation along they dimension can allow different
lanes of a flow cell to be addressed. When a lane is wider than the
field of view for the objective, y translation can be used to
detect multiple swaths of the lane (i.e. a first swath can be
detected by a scan along x and a second swath can be addressed by a
step along the y dimension followed by a second scan along x). A y
actuator can be configured similarly to the x actuators exemplified
herein. For example, a y actuator can be configured to translate
the flow cell while it is urged to a reference surface by a
preload. Other stepper motors or translation actuators can be used
as well for x or y translation.
[0074] In particular embodiments, an apparatus of the present
disclosure can include a rotational actuator configured to change
the relative translational position of the detector and the vessel
along an arcuate path. Taking the exemplary flow cell oriented as
shown in FIG. 1 a rotational actuator can rotate the flow cell in
the yaw axis. Rotation in the yaw axis can be particularly useful
for scanning lanes or features that follow an arcuate path. An
additional or alternative rotational actuator can rotate a vessel
along the roll axis. Rotation in the yaw axis can be particularly
useful when the vessel is a tube or cylinder that is oriented to
have its length along the x axis.
[0075] Several embodiments of the present disclosure are
exemplified with regard to an objective having several lenses for
gathering and focusing radiation from an object (e.g. a vessel such
as a flow cell). It will be understood that any of a variety of
optical elements can serve as an objective in an apparatus or
method of the present disclosure including, for example, a lens,
mirror, fiber optic, fiber bundle, lens array or other optical
element that gathers radiation from an object being observed,
whether or not the optical element is also capable of focusing the
radiation. Objectives or other optical components used in an
apparatus or method set forth herein can be configured to transmit
radiation in any of a variety of spectral ranges including, but not
limited to X-ray, ultraviolet (UV), visible (VIS), infrared (IR),
microwave and/or radio wave ranges.
[0076] An objective that is used in an apparatus set forth herein
can be placed to direct radiation from the internal surface or the
lumen of a vessel, through the wall of the vessel and to a detector
when the external surface of the vessel contacts a reference
surface. In particular embodiments, an objective, and other
optional components of an optical system, can be configured for
epi-illumination luminescence detection (i.e. epi-luminescence),
whereby excitation radiation is directed from a radiation source,
through the objective, then through the wall of the vessel to the
internal surface or the lumen of the vessel; and whereby emission
from the internal surface or the lumen of the vessel is directed
back through the wall and through the objective (i.e. excitation
and emission both pass through the objective). Alternatively,
objectives, and other optional components of an optical system, can
be configured for trans-illumination fluorescence, whereby
excitation radiation is directed from a radiation source through a
first wall of a vessel to the internal surface or the lumen of the
vessel; and whereby emission from the internal surface or the lumen
of the vessel is directed through another wall of the vessel and
through the objective (i.e. emission passes through the objective,
excitation does not). Other useful configurations for fluorescence
detection include those that excite a vessel via total internal
reflection fluorescence (TIRF) or via waveguides. In any of a
variety of configurations, the radiation source can form a
structural loop with a reference surface such that a vessel that
contacts the reference under the urging of a preload will be
properly oriented with respect to the radiation source.
[0077] The objectives shown in FIGS. 2, 3, 5 and 6 are exemplary,
having 4 lenses. Any number or type of lenses can be included to
suit a particular application. Particularly useful objectives will
have a numerical aperture that is at least 0.1 and at most 0.9.
Numerical apertures above 0.95 can be achieved using an immersion
objective as set forth in further detail below. An objective or
other transmitter can be configured to operate with a detection
system that resolves features (e.g. nucleic acid sites) on a
surface that are separated by less than 100 .mu.m, 50 .mu.m, 10
.mu.m, 5 .mu.m, 1 .mu.m, or 0.5 .mu.m. The detection system,
including objective or other transmitter, can be configured to
resolve features having an area on a surface that is smaller than
about 1 mm.sup.2, 500 .mu.m.sup.2, 100 .mu.m.sup.2, 25 .mu.m.sup.2,
10 .mu.m.sup.2, 5 .mu.m.sup.2, 1 .mu.m.sup.2, 500 nm.sup.2, or 100
nm.sup.2.
[0078] An optical system used in an apparatus or method set forth
herein can have a field of view that is at least 0.1 mm.sup.2, 0.5
mm.sup.2, 1 mm.sup.2, 2 mm.sup.2, 3 mm.sup.2, 4 mm.sup.2 or higher.
Alternatively and/or additionally, the field of view can be
configured to be at most 4 mm.sup.2, 3 mm.sup.2, 2 mm.sup.2, 1
mm.sup.2, 0.5 mm.sup.2, 0.1 mm.sup.2, or less.
[0079] The objective, or other appropriate component of a detection
system used in an apparatus set forth herein, can be configured to
focus on analytes that are in or on the vessel. For example, the
apparatus can include a focus actuator configured to change the
relative position of the objective and the reference surface in the
focus dimension z. Physically aligning the vessel to the reference
surface under force of a preload effectively fixes the position of
the vessel in the z dimension, thereby favoring accurate and robust
focusing throughout a scanning operation.
[0080] An apparatus set forth herein can employ optical sub-systems
or components used in nucleic acid sequencing systems. Several such
detection apparatus are configured for optical detection, for
example, detection of fluorescent signals. Examples of detection
apparatus and components thereof that can be used to detect a
vessel herein are described, for example, in US Pat. App. Pub. No.
2010/0111768 A1 or U.S. Pat. Nos. 7,329,860; 8,951,781 or
9,193,996, each of which is incorporated herein by reference. Other
detection apparatus include those commercialized for nucleic acid
sequencing such as those provided by Illumina.TM., Inc. (e.g.
HiSeg.TM., MiSeg.TM., NextSeg.TM., or NovaSeg.TM. systems), Life
Technologies.TM. (e.g. ABI PRISM .TM., or SOLiD.TM. systems),
Pacific Biosciences (e.g. systems using SMRT.TM. Technology such as
the Sequel.TM. or RS II.TM. systems), or Qiagen (e.g.
Genereader.TM. system). Other useful detectors are described in
U.S. Pat. Nos. 5,888,737; 6,175,002; 5,695,934; 6,140,489; or
5,863,722; or US Pat. Pub. Nos. 2007/007991 A1, 2009/0247414 A1, or
2010/0111768; or W02007/123744, each of which is incorporated
herein by reference in its entirety. In particular embodiments, the
stage of a known sequencing system can be replaced with a scanning
apparatus set forth herein.
[0081] Generally, an objective is the optical element of the
detection apparatus that is proximal (i.e. closest to) the vessel
that is to be detected (e.g. flow cell). In some embodiments, the
vessel need not include any optical components. In alternative
embodiments, one or more optical component, such as a lens or fiber
optic, can be provided by a vessel or by a cartridge to which the
vessel is attached. For example, the objective of the detection
apparatus can be configured to direct excitation, emission or other
signals to the optical component that is present on the vessel or
cartridge. Thus, the optical component that is proximal to the
sample can be provided by the detection apparatus, or
alternatively, by the vessel that houses the sample.
[0082] A detection apparatus that is used to observe a vessel in a
method or apparatus set forth herein need not be capable of optical
detection. For example, the detector can be an electronic detector
used for detection of protons or pyrophosphate (see, for example,
US Pat. App. Pub. Nos. 2009/0026082 A1; 2009/0127589 A1;
2010/0137143 A1; or 2010/0282617 A1, each of which is incorporated
herein by reference in its entirety, or the Ion Torrent.TM. systems
commercially available from ThermoFisher, Waltham, Mass.) or as
used in detection of nanopores such as those commercialized by
Oxford Nanopore.TM., Oxford UK (e.g. MinION.TM. or PromethION.TM.
systems) or set forth in U.S. Pat. No. 7,001,792; Soni &
Meller, Clin. Chem. 53, 1996-2001 (2007); Healy, Nanomed. 2,
459-481 (2007); or Cockroft, et al. J. Am. Chem. Soc. 130, 818-820
(2008), each of which is incorporated herein by reference.
[0083] In a particular embodiments, apparatus or methods set forth
herein can be configured for scanning electron microscopy (SEM).
Accordingly, an electron beam can be produced by an electron gun
and directed to a vessel by one or more condenser lenses, scanning
coils and/or deflector plates. Signal can be detected using an
electron detector such as a scintillator-photomultiplier system
(e.g. an Everhart-Thornley detector).
[0084] In particular embodiments, a detection apparatus or other
apparatus of the present disclosure can provide temperature control
of a vessel that is to be detected. Temperature control can be
provided by controlling temperature of an internal chamber that
houses the vessel. Alternatively or additionally, a vessel that is
to be detected can be placed into contact with a thermally
conductive surface that is temperature controlled. FIG. 7A shows an
exemplary configuration for achieving temperature control of a flow
cell via contact with a thermally conductive surface. The backside
of aluminum body 460 is attached to two thermal elements 450 and
451 which are located left and right of conical depression 416. The
thermal elements can be polyimide thermofoil heaters, Peltier
elements, metal heating elements, ceramic heating elements, polymer
PTC heating elements or the like. Aluminum body 460 also includes
two legs 461 and 462 for attachment to the detection apparatus. As
such the two legs form part of the structural loop between the
reference surface on the aluminum body 460 and the detection
apparatus. Optionally, legs 461 and 462 can be made from a material
having low thermal conductivity. Thus, the legs can function to
attach the aluminum body to a detection apparatus in a way that
insulates other components of the detection apparatus from
experiencing unwanted temperature fluctuations. Thermal elements
450 and 451 can be activated via wires 452 and 453 to heat or cool
aluminum body 460 such that a flow cell in cartridge 400 is in
contact with the opposite side of aluminum body 460 and thus is
temperature controlled. As shown in FIG. 7B, conical depression 416
is configured to accept an objective 410 for detection of a flow
cell in cartridge 400 through window 418. In the configuration
shown, the flow cell cartridge 400 is translated via film sprocket
420 under the control of rotary motor 425.
[0085] A detection apparatus or other apparatus of the present
disclosure can include a fluidics system for delivering reagents to
a vessel that is to be detected. Accordingly, one or more
reservoirs can be fluidically connected to an inlet valve of the
vessel. The apparatus can further include a pressure supply for
driving reagents from reservoirs to the vessel. The apparatus can
include a waste reservoir that is fluidically connected to the
vessel to remove spent reagents. Taking as an example an embodiment
where the vessel is a flow cell, reagents can be delivered via pump
to the flow cell through the inlet and then the reagents can flow
through the flow cell outlet to a waste reservoir. The reservoirs
can include reagents for any of a variety of analytical procedures
including, but not limited to nucleic acid sequencing, nucleic acid
genotyping, nucleic acid expression analysis, protein sequencing,
protein binding analysis (e.g. ELISA), small molecule receptor
binding, protein phosphorylation analysis, nucleic acid synthesis
or protein synthesis. Alternatively or additionally, the reservoirs
can include reagents for a preparative process. Exemplary
preparative processes include, but are not limited to, nucleic acid
synthesis, peptide synthesis, assembly of oligonucleotides into
genes, photolithography, nanofabrication or microfabrication (e.g.
via laser etching), laser ablation, or the like.
[0086] A fluidic system can include at least one manifold and/or at
least one valve for directing reagents from reservoirs to a vessel
where detection occurs. Manifolds are particularly useful in
sequencing instruments due to the relatively large number of
different reagents that are delivered during a sequencing protocol.
Exemplary protocols and useful reagents are set forth in further
detail below and in references that are incorporated herein by
reference. Fluid flow from the reservoirs can be selected via
valves such as a solenoid valve (e.g. those made by Takasago
Electric, Japan), ball valve, diaphragm valve or rotary valve.
[0087] One or more fluidic components used in a detection apparatus
or other apparatus of the present disclosure can be housed in a
fluidic caddy that is separable from detection components. An
exemplary fluidic caddy 600 is shown in FIG. 8A. Fluidic caddy 600
includes a housing 601 having sufficient internal volume to house
reagent reservoirs 603, waste reservoirs 602, and a piston shaft
604 for an external pump. Any of a variety of fluidic components
can be housed in a fluidic caddy including, but not limited to, one
or more reservoirs, fluid lines, valves or pumps. The fluidic caddy
includes latches 610 and 611 which are configured to engage with
hooks in a detection apparatus. See for example, switch hook 701 in
FIG. 9. Flow cell 430 is held within cartridge 400 and cartridge
400 is held to the fluidic caddy 600 via hook 616 and guides 616
and 617. As shown in the expanded cutout of FIG. 8B and in
side-view FIG. 8D, hook 615 includes a tooth 614 that inserts into
track 401 to hold the cartridge 400 in place. Guides 616 and 617
complete a three-point attachment by engaging the bottom edge of
cartridge 400. Preload 620, although shown in retracted position in
FIG. 8D, can be extended to push against the back side of the
cartridge 400, thereby functioning with hook 615 and guides 616 and
617 to hold the cartridge in place by compressive forces.
[0088] Fluidic caddy 600 includes openings as shown in FIG. 8D and
FIG. 8F. For purposes of showing fluidic connections for the flow
cell 430, FIG. 8F shows a perspective view of caddy 600 that has
been emptied of several other fluidic components. Opening 605 is
configured to accept the piston of an external pump. The piston can
be driven by a detection apparatus to allow control of fluid flow
through flow cell 430 during an analytical procedure (e.g. a
nucleic acid sequencing procedure), but the piston need not
directly contact any fluids in the caddy 600 or in the flow cell
430. Accordingly, the detection apparatus can constitute a "dry"
component that does not make direct contact with fluids, whereas
the caddy 600 and flow cell 430 constitute "wet" components.
Fluidic caddy 600 includes two elongated openings 621 and 622 which
are configured to accommodate tubes 661 and 662, respectively. The
elongated shape allows the tubes to move along the x dimension as
the flow cell is translated during scanning. Thus, the tubes can
remain engaged with the flow cell and fluidic reservoirs during a
scanning operation.
[0089] The flow cell 430 can be translated independently of caddy
600 via movement of the cartridge as set forth previously herein,
for example, in connection with FIG. 4. As such, caddy 600 remains
stationary while flow cell 430 is moved. Alternatively, a flow cell
can be attached to a caddy such that the caddy and flow cell are
translated as a unit. In a further alternative, one or more
detection components of a detection apparatus can be moved while
the flow cell and/or fluidic caddy is stationary.
[0090] Interactions between fluidic caddy 600 and components of a
detection apparatus are shown in FIG. 9. The perspective view in
FIG. 9A and top view in FIG. 9B, show caddy 600 engaged in a way
that sandwiches flow cell cartridge 400 between the caddy 600 and
aluminum body 460. When engaged, the flow cell cartridge 400
contacts film sprocket 420 such that motor 425 can drive
translation of the flow cell therein. Translation will cause the
flow cell to move past objective 721 which is in turn configured to
direct fluorescence excitation from fluorometer 720 to the flow
cell and to direct fluorescence emission from the flow cell to
fluorometer 720.
[0091] The mechanism of engaging caddy 600 and flow cell cartridge
400 with a detection apparatus or other apparatus of the present
disclosure can be akin to inserting an 8-track cassette into an
audio player. The flow cell 430 and cartridge 400 are connected to
caddy 600 such that a user need not directly handle the flow cell
430, instead delivering it to the detection apparatus by handling
the caddy 600, much like a user need not handle the tape inside of
the 8-track cassette. Similarly, individual fluidic components need
not be individually handled but can properly engage with actuators
in the detection apparatus when the caddy 600 is properly placed in
the detection apparatus.
[0092] Fluidic caddy 600 is disengaged from the detection apparatus
in FIG. 9C, which illustrates mechanical elements that can be used
by the detection apparatus to control function of the fluidic caddy
600. The detection apparatus can include a sensor or switch that
responds to presence of the fluidic caddy and actuates functional
interactions. In the example of FIG. 9, switch hook 701 is
displaced when caddy 600 is properly engaged. This displacement can
activate one or more functions. For example, the underside of
fluidic caddy 600 can include one or more openings that are
positioned to accept one or more valve actuator 711 on platform
710. Valve actuators, although shown in the proud position for
purposes of illustration, can be retracted into platform 710 when
fluidic caddy 600 is not present. The valve actuators can be raised
in response to displacement of switch hook 701 and/or in response
to control software for the detection apparatus. Accordingly, the
one or more valve actuator 711 can be used to control flow of
fluids to the flow cell, from the flow cell, and/or between
reservoirs within the caddy. In another example, pump component 702
of the detection apparatus can engage with fluidic components of
the caddy 600 via opening 710, for example, by inserting a piston.
Interaction of pump component 702 with the fluidic caddy 600 can be
actuated directly due to displacement of switch hook 701 and/or in
response to control software for the detection apparatus.
[0093] The structural loop between the flow cell 430 and
fluorometer 720 includes reference surface 417, aluminum body 460,
legs 461 and 462, a plate or base to which legs 461 and 462 are
attached, and fluorometer 720 which is also attached to the plate
or base.
[0094] FIG. 10 shows a mechanism that can be used for engaging a
flow cell with a detection apparatus. FIG. 10A shows a side view
and expanded detail of fluidic cartridge 600 and flow cell
cartridge 400 when not engaged with a detection apparatus. When the
fluidic caddy 600 is not engaged, flow cell cartridge 400 is in
contact with hook 615 and guides 616 and 617. FIG. 10B shows an
expanded detail of the configuration that results when caddy 600 is
engaged with the detection apparatus. Specifically, flow cell
cartridge 400 is moved toward the wall of caddy 600, disengaging
from hook 615 and from guides 616 and 617.
[0095] A mechanism for changing the position of the flow cell
cartridge 400 is shown in FIG. 10E, which is a detail view of the
interface between caddy 600, flow cell cartridge 400 and aluminum
body 460. FIG. 10E is a detail of FIG. 10D which is a cutaway along
line m in FIG. 10C. When the caddy 600 is properly engaged with the
detection apparatus, hook 615 and guides 616 and 617 are inserted
into notches 471, 472 and 473 in aluminum body 460. The notches
471, 472 and 473 have a sufficient depth that compression of the
caddy toward the aluminum body 460 causes the front side of flow
cell cartridge 400 to engage sprocket 420 and the front side of
flow cell 430 to contact reference surface 417. The compression
also results in the back side of flow cell cartridge 400 contacting
compression foot 102. In this way, the flow cell 430 is pressed
against the reference surface 417 for alignment with objective 410,
which observes the flow cell 430 through window 418. The flow cell
430 can be translated via interaction of sprocket 420 with
perforation track 401.
[0096] Although interactions between a fluidic caddy and detection
apparatus have been exemplified herein using mechanical contacts,
it will be understood that other mechanical switching mechanisms
can be used. Electronic switches can also be used, including for
example, those that are activated by electronic sensors (e.g.
Bluetooth), magnetic sensors, radio frequency sensors (e.g. RFID),
pressure sensors, optical sensors (e.g. barcodes) or the like.
[0097] The fluidic caddy and components set forth above are
exemplary. Other fluidic caddies and fluidic components that can be
used with a detection apparatus of the present disclosure are set
forth in commonly owned U.S. patent application Ser. No.
15/922,661, which claims the benefit of U.S. Provisional App. No.
62/481,289, and US Pat. App. Pub. No. 2017/0191125 A1, each of
which is incorporated herein by reference. Moreover, a similar
fluidic caddy can be used with other apparatus of the present
disclosure, such as reactor apparatus, and the other apparatus can
be configured as set forth above to interface with a caddy.
[0098] Optionally, a detection apparatus or other apparatus of the
present disclosure can further include a computer processing unit
(CPU) that is configured to operate one or more of the system
components set forth herein. The same or different CPU can interact
with the system to acquire, store and process signals (e.g. signals
detected in a method set forth herein). In particular embodiments,
a CPU can be used to determine, from the signals, the identity of
the nucleotide that is present at a particular location in a
template nucleic acid. In some cases, the CPU will identify a
sequence of nucleotides for the template from the signals that are
detected.
[0099] A useful CPU can include, for example, one or more of a
personal computer system, server computer system, thin client,
thick client, hand-held or laptop device, multiprocessor system,
microprocessor-based system, set top box, programmable consumer
electronic, network PC, minicomputer system, mainframe computer
system, smart phone, or distributed cloud computing environment
that includes any of the above systems or devices. The CPU can
include one or more processors or processing units, a memory
architecture that may include RAM and non-volatile memory. The
memory architecture may further include removable/non-removable,
volatile/non-volatile computer system storage media. Further, the
memory architecture may include one or more readers for reading
from and writing to a non-removable, non-volatile magnetic media,
such as a hard drive, a magnetic disk drive for reading from and
writing to a removable, non-volatile magnetic disk, and/or an
optical disk drive for reading from or writing to a removable,
non-volatile optical disk such as a CD-ROM or DVD-ROM. The CPU may
also include a variety of computer system readable media. Such
media may be any available media that is accessible by a cloud
computing environment, such as volatile and non-volatile media, and
removable and non-removable media.
[0100] The memory architecture may include at least one program
product having at least one program module implemented as
executable instructions that are configured to control one or more
component of an apparatus set forth herein or to carry out one or
more portions of a method set forth herein. For example, executable
instructions may include an operating system, one or more
application programs, other program modules, and program data.
Generally, program modules may include routines, programs, objects,
components, logic, data structures, and so on, that perform
particular tasks such as processing of signals detected in a method
set forth herein.
[0101] The components of a CPU may be coupled by an internal bus
that may be implemented as one or more of any of several types of
bus structures, including a memory bus or memory controller, a
peripheral bus, an accelerated graphics port, and a processor or
local bus using any of a variety of bus architectures. By way of
example, and not limitation, such architectures include Industry
Standard Architecture (ISA) bus, Micro Channel Architecture (MCA)
bus, Enhanced ISA (EISA) bus, Video Electronics Standards
Association (VESA) local bus, and Peripheral Component
Interconnects (PCI) bus.
[0102] A CPU can optionally communicate with one or more external
devices such as a keyboard, a pointing device (e.g. a mouse), a
display, such as a graphical user interface (GUI), or other device
that facilitates interaction of a user with the nucleic acid
detection system. Similarly, the CPU can communicate with other
devices (e.g., via network card, modem, etc.). Such communication
can occur via I/O interfaces. Furthermore, a CPU of a system herein
may communicate with one or more networks such as a local area
network (LAN), a general wide area network (WAN), and/or a public
network (e.g., the Internet) via a suitable network adapter.
[0103] FIG. 11 shows a cutaway profile view of an exemplary optical
arrangement that uses immersion optics. The arrangement includes an
objective 710 that includes a housing 720 and several lenses 711,
712 and 715. The number, position and shape of the lenses is
exemplary and can vary according to desired prescription. Also
included is rigid body 700, flow cell 701 and flow cell cartridge
702. Flow cell cartridge 702 includes inlet 741 and outlet 742 for
moving fluid reagents into and out of the flow cell. The bottom
side of rigid body 700 has a reference surface 717 that becomes
sealed by flow cell 710 when a preload is applied, for example, as
set forth using configurations set forth above. Opposite this seal,
rigid body 700 includes a conical depression 716 that is shaped to
accept the tip of objective 710. The space 716 between rigid body
700, objective 710 and the seal can be filled with an immersion
fluid, such as an oil or aqueous solvent that is index matched to
the objective. As such, the immersion fluid will directly contact
the proximal lens 715 of objective 710 and the surface of flow cell
701. The fluid can be maintained in the space 716 by seals 731 and
732, which are optionally flexible. Fluid can be added and/or
removed from space 716 via line 733. Immersion optics can provide
several advantages over optics that image through air including,
for example, the ability to achieve numerical aperture (NA) greater
than 0.95, ability to image at greater depths into a vessel, and
alleviating tolerances on the thickness and uniformity of vessel
walls through which the objective resolves objects.
[0104] The present disclosure provides methods that are
particularly useful for performing cyclical reactions. Each cycle
can include delivering reagents for the reaction to a flow cell or
other vessel where, optionally, the reaction, or products of the
reaction, will be observed. Each cycle can further include scanning
of the vessel using apparatus or methods set forth herein. The
methods are exemplified herein in the context of a nucleic acid
sequencing reaction. However, those skilled in the art will
understand from the teaching herein how to modify the methods, and
the apparatus, for other cyclical reactions such as nucleic acid
synthesis reactions, peptide sequencing reactions, peptide
synthesis reactions, combinatorial small molecule synthesis
reactions or the like. However, the method need not be cyclical and
can instead be carried out in a non-repetitive configuration, for
example, to observe a single reaction or phenomenon.
[0105] Particularly useful sequencing reactions are Sequencing By
Binding.TM. (SBB.TM.) reactions as described in commonly owned US
Pat. App. Pub. No. 2017/0022553 A1; U.S. Pat. App. Ser. No.
62/447,319 to which US Pat App. Pub. No. 2018/0044727 A1 claims
priority; 62/440,624 to which US Pat App. Pub. No. 2018/0187245 A1
claims priority; or 62/450,397 to which US Pat App. Pub. No.
2018/0208983 A1 claims priority, each of which is incorporated
herein by reference. Generally, methods for determining the
sequence of a template nucleic acid molecule can be based on
formation of a ternary complex (between polymerase, primed nucleic
acid and cognate nucleotide) under specified conditions. The method
can include an examination phase followed by a nucleotide
incorporation phase.
[0106] The examination phase can be carried out in a flow cell (or
other vessel), the flow cell containing at least one template
nucleic acid molecule primed with a primer by delivering to the
flow cell reagents to form a first reaction mixture. The reaction
mixture can include the primed template nucleic acid, a polymerase
and at least one nucleotide type. Interaction of polymerase and a
nucleotide with the primed template nucleic acid molecule(s) can be
observed under conditions where the nucleotide is not covalently
added to the primer(s); and the next base in each template nucleic
acid can be identified using the observed interaction of the
polymerase and nucleotide with the primed template nucleic acid
molecule(s). The interaction between the primed template,
polymerase and nucleotide can be detected in a variety of schemes.
For example, the nucleotides can contain a detectable label. Each
nucleotide can have a distinguishable label with respect to other
nucleotides. Alternatively, some or all of the different nucleotide
types can have the same label and the nucleotide types can be
distinguished based on separate deliveries of different nucleotide
types to the flow cell. In some embodiments, the polymerase can be
labeled. Polymerases that are associated with different nucleotide
types can have unique labels that distinguish the type of
nucleotide to which they are associated. Alternatively, polymerases
can have similar labels and the different nucleotide types can be
distinguished based on separate deliveries of different nucleotide
types to the flow cell. Detection can be carried out by scanning
the flow cell using an apparatus or method set forth herein.
[0107] During the examination phase, discrimination between correct
and incorrect nucleotides can be facilitated by ternary complex
stabilization. A variety of conditions and reagents can be useful.
For example, the primer can contain a reversible blocking moiety
that prevents covalent attachment of nucleotide; and/or cofactors
that are required for extension, such as divalent metal ions, can
be absent; and/or inhibitory divalent cations that inhibit
polymerase-based primer extension can be present; and/or the
polymerase that is present in the examination phase can have a
chemical modification and/or mutation that inhibits primer
extension; and/or the nucleotides can have chemical modifications
that inhibit incorporation, such as 5' modifications that remove or
alter the native triphosphate moiety. The examination phase can
include scanning of the flow cell using apparatus and methods set
forth herein.
[0108] The extension phase can then be carried out by creating
conditions in the flow cell where a nucleotide can be added to the
primer on each template nucleic acid molecule. In some embodiments,
this involves removal of reagents used in the examination phase and
replacing them with reagents that facilitate extension. For
example, examination reagents can be replaced with a polymerase and
nucleotide(s) that are capable of extension. Alternatively, one or
more reagents can be added to the examination phase reaction to
create extension conditions. For example, catalytic divalent
cations can be added to an examination mixture that was deficient
in the cations, and/or polymerase inhibitors can be removed or
disabled, and/or extension competent nucleotides can be added,
and/or a deblocking reagent can be added to render primer(s)
extension competent, and/or extension competent polymerase can be
added.
[0109] It will be understood that any of a variety of nucleic acid
sequencing reactions can be carried out using an apparatus and
method of the present disclosure. Other exemplary sequencing
methods are set forth below.
[0110] Sequencing-by-synthesis (SBS) techniques can be used. SBS
generally involves the enzymatic extension of a nascent primer
through the iterative addition of nucleotides against a template
strand to which the primer is hybridized. Briefly, SBS can be
initiated by contacting target nucleic acids, attached to sites in
a vessel, with one or more labeled nucleotides, DNA polymerase,
etc. Those sites where a primer is extended using the target
nucleic acid as template will incorporate a labeled nucleotide that
can be detected. Detection can include scanning using an apparatus
or method set forth herein. Optionally, the labeled nucleotides can
further include a reversible termination property that terminates
further primer extension once a nucleotide has been added to a
primer. For example, a nucleotide analog having a reversible
terminator moiety can be added to a primer such that subsequent
extension cannot occur until a deblocking agent is delivered to
remove the moiety. Thus, for embodiments that use reversible
termination, a deblocking reagent can be delivered to the vessel
(before or after detection occurs). Washes can be carried out
between the various delivery steps. The cycle can be performed n
times to extend the primer by n nucleotides, thereby detecting a
sequence of length n. Exemplary SBS procedures, reagents and
detection components that can be readily adapted for use with a
detection apparatus produced by the methods of the present
disclosure are described, for example, in Bentley et al., Nature
456:53-59 (2008), WO 04/018497; WO 91/06678; WO 07/123744; U.S.
Pat. Nos. 7,057,026; 7,329,492; 7,211,414; 7,315,019 or 7,405,281,
and US Pat. App. Pub. No. 2008/0108082 A1, each of which is
incorporated herein by reference. Also useful are SBS methods that
are commercially available from Illumina, Inc. (San Diego,
Calif.).
[0111] Some SBS embodiments include detection of a proton released
upon incorporation of a nucleotide into an extension product. For
example, sequencing based on detection of released protons can use
reagents and an electrical detector that are commercially available
from ThermoFisher (Waltham, Mass.) or described in US Pat. App.
Pub. Nos. 2009/0026082 A1; 2009/0127589 A1; 2010/0137143 A1; or
2010/0282617 A1, each of which is incorporated herein by
reference.
[0112] Other sequencing procedures can be used, such as
pyrosequencing. Pyrosequencing detects the release of inorganic
pyrophosphate (PPi) as nucleotides are incorporated into a nascent
primer hybridized to a template nucleic acid strand (Ronaghi, et
al., Analytical Biochemistry 242 (1), 84-9 (1996); Ronaghi, Genome
Res. 11 (1), 3-11 (2001); Ronaghi et al. Science 281 (5375), 363
(1998); U.S. Pat. Nos. 6,210,891; 6,258,568 and 6,274,320, each of
which is incorporated herein by reference). In pyrosequencing,
released PPi can be detected by being converted to adenosine
triphosphate (ATP) by ATP sulfurylase, and the resulting ATP can be
detected via luciferase-produced photons. Thus, the sequencing
reaction can be monitored via a luminescence detection system that
is configured to scan a vessel using apparatus and methods set
forth herein.
[0113] Sequencing-by-ligation reactions are also useful including,
for example, those described in Shendure et al. Science
309:1728-1732 (2005); U.S. Pat. Nos. 5,599,675; or 5,750,341, each
of which is incorporated herein by reference. Some embodiments can
include sequencing-by-hybridization procedures as described, for
example, in Bains et al., Journal of Theoretical Biology 135 (3),
303-7 (1988); Drmanac et al., Nature Biotechnology 16, 54-58
(1998); Fodor et al., Science 251 (4995), 767-773 (1995); or WO
1989/10977, each of which is incorporated herein by reference. In
both sequencing-by-ligation and sequencing-by-hybridization
procedures, primers that are hybridized to nucleic acid templates
are subjected to repeated cycles of extension by oligonucleotide
ligation. Typically, the oligonucleotides are fluorescently labeled
and can be detected to determine the sequence of the template, for
example, using a scanning apparatus or method set forth herein.
[0114] Some embodiments can utilize methods involving real-time
monitoring of DNA polymerase activity. For example, nucleotide
incorporations can be detected through fluorescence resonance
energy transfer (FRET) interactions between a fluorophore-bearing
polymerase and gamma-phosphate-labeled nucleotides, or with
zero-mode waveguides (ZMW). Techniques and reagents for sequencing
via FRET and or ZMW detection that can be modified for use in an
apparatus or method set forth herein are described, for example, in
Levene et al. Science 299, 682-686 (2003); Lundquist et al. Opt.
Lett. 33, 1026-1028 (2008); Korlach et al. Proc. Natl. Acad. Sci.
USA 105, 1176-1181 (2008); or U.S. Pat. Nos. 7,315,019; 8,252,911
or 8,530,164, the disclosures of which are incorporated herein by
reference.
[0115] Steps for the above sequencing methods can be carried out
cyclically. For example, examination and extension steps of an
SBB.TM. method can be repeated such that in each cycle a single
next correct nucleotide is examined (i.e. the next correct
nucleotide being a nucleotide that correctly binds to the
nucleotide in a template nucleic acid that is located immediately
5' of the base in the template that is hybridized to the 3'-end of
the hybridized primer) and, subsequently, a single next correct
nucleotide is added to the primer. Any number of cycles of a
sequencing method set forth herein can be carried out including,
for example, at least 1, 2, 5, 10, 20, 25, 30, 40, 50, 75, 100, 150
or more cycles. Alternatively or additionally, no more than 150,
100, 75, 50, 40, 30, 25, 20, 10, 5, 2 or 1 cycles are carried
out.
[0116] Nucleic acid template(s), to be sequenced, can be added to a
vessel using any of a variety of known methods. In some
embodiments, a single nucleic acid molecule is to be sequenced. The
nucleic acid molecule can be delivered to a vessel and can
optionally be attached to a surface in the vessel. In some
embodiments, the molecule is subjected to single molecule
sequencing. Alternatively, multiple copies of the nucleic acid can
be made and the resulting ensemble can be sequenced. For example,
the nucleic acid can be amplified on a surface (e.g. on the inner
wall of a flow cell) using techniques set forth in further detail
below.
[0117] In multiplex embodiments, a variety of different nucleic
acid molecules (i.e. a population having a variety of different
sequences) are sequenced. The molecules can optionally be attached
to a surface in a vessel. The nucleic acids can be attached at
unique sites on the surface and single nucleic acid molecules that
are spatially distinguishable one from the other can be sequenced
in parallel. Alternatively, the nucleic acids can be amplified on
the surface to produce a plurality of surface attached ensembles.
The ensembles can be spatially distinguishable and sequenced in
parallel.
[0118] A method set forth herein can use any of a variety of
amplification techniques in a vessel. Exemplary techniques that can
be used include, but are not limited to, polymerase chain reaction
(PCR), rolling circle amplification (RCA), multiple displacement
amplification (MDA), bridge amplification, or random prime
amplification (RPA). In particular embodiments, one or more primers
used for amplification can be attached to a surface in a vessel. In
such embodiments, extension of the surface-attached primers along
template nucleic acids will result in copies of the templates being
attached to the surface. Methods that result in one or more sites
on a solid support, where each site is attached to multiple copies
of a particular nucleic acid template, can be referred to as
"clustering" methods.
[0119] In PCR embodiments, one or both primers used for
amplification can be attached to a surface. Formats that utilize
two species of attached primer are often referred to as bridge
amplification because double stranded amplicons form a bridge-like
structure between the two attached primers that flank the template
sequence that has been copied. Exemplary reagents and conditions
that can be used for bridge amplification are described, for
example, in U.S. Pat. Nos. 5,641,658 or 7,115,400; U.S. Patent Pub.
Nos. 2002/0055100 A1, 2004/0096853 A1, 2004/0002090 A1,
2007/0128624 A1 or 2008/0009420 A1, each of which is incorporated
herein by reference. PCR amplification can also be carried out with
one of the amplification primers attached to the surface and the
second primer in solution. An exemplary format that uses a
combination of one solid phase-attached primer and a solution phase
primer is known as primer walking and can be carried out as
described in U.S. Pat. No. 9,476,080, which is incorporated herein
by reference. Another example is emulsion PCR which can be carried
out as described, for example, in Dressman et al., Proc. Natl.
Acad. Sci. USA 100:8817-8822 (2003), WO 05/010145, or U.S. Patent
Pub. Nos. 2005/0130173 A1 or 2005/0064460 A1, each of which is
incorporated herein by reference.
[0120] RCA techniques can be used in a method set forth herein.
Exemplary reagents that can be used in an RCA reaction and
principles by which RCA produces amplicons are described, for
example, in Lizardi et al., Nat. Genet. 19:225-232 (1998) or US
Pat. App. Pub. No. 2007/0099208 A1, each of which is incorporated
herein by reference. Primers used for RCA can be in solution or
attached to a surface in a flow cell.
[0121] MDA techniques can also be used in a method of the present
disclosure. Some reagents and useful conditions for MDA are
described, for example, in Dean et al., Proc Natl. Acad. Sci. USA
99:5261-66 (2002); Lage et al., Genome Research 13:294-307 (2003);
Walker et al., Molecular Methods for Virus Detection, Academic
Press, Inc., 1995; Walker et al., Nucl. Acids Res. 20:1691-96
(1992); or U.S. Pat. Nos. 5,455,166; 5,130,238; or 6,214,587, each
of which is incorporated herein by reference. Primers used for MDA
can be in solution or attached to a surface in a vessel.
[0122] In particular embodiments, a combination of the
above-exemplified amplification techniques can be used. For
example, RCA and MDA can be used in a combination wherein RCA is
used to generate a concatemeric amplicon in solution (e.g. using
solution-phase primers). The amplicon can then be used as a
template for MDA using primers that are attached to a surface in a
vessel. In this example, amplicons produced after the combined RCA
and MDA steps will be attached in the vessel. The amplicons will
generally contain concatemeric repeats of a target nucleotide
sequence.
[0123] Nucleic acid templates that are used in a method or
composition herein can be DNA such as genomic DNA, synthetic DNA,
amplified DNA, complementary DNA (cDNA) or the like. RNA can also
be used such as mRNA, ribosomal RNA, tRNA or the like. Nucleic acid
analogs can also be used as templates herein. Thus, a mixture of
nucleic acids used herein can be derived from a biological source,
synthetic source or amplification product. Primers used herein can
be DNA, RNA or analogs thereof.
[0124] Exemplary organisms from which nucleic acids can be derived
include, for example, those from a mammal such as a rodent, mouse,
rat, rabbit, guinea pig, ungulate, horse, sheep, pig, goat, cow,
cat, dog, primate, human or non-human primate; a plant such as
Arabidopsis thaliana, corn, sorghum, oat, wheat, rice, canola, or
soybean; an algae such as Chlamydomonas reinhardtii; a nematode
such as Caenorhabditis elegans; an insect such as Drosophila
melanogaster, mosquito, fruit fly, honey bee or spider; a fish such
as zebrafish; a reptile; an amphibian such as a frog or Xenopus
laevis; a Dictyostelium discoideum; a fungi such as Pneumocystis
carinii, Takifugu rubripes, yeast, Saccharamoyces cerevisiae or
Schizosaccharomyces pombe; or a Plasmodium falciparum. Nucleic
acids can also be derived from a prokaryote such as a bacterium,
Escherichia coli, Staphylococci or Mycoplasma pneumoniae; an
archae; a virus such as Hepatitis C virus or human immunodeficiency
virus; or a viroid. Nucleic acids can be derived from a homogeneous
culture or population of the above organisms or alternatively from
a collection of several different organisms, for example, in a
community or ecosystem. Nucleic acids can be isolated using methods
known in the art including, for example, those described in
Sambrook et al., Molecular Cloning: A Laboratory Manual, 3rd
edition, Cold Spring Harbor Laboratory, New York (2001) or in
Ausubel et al., Current Protocols in Molecular Biology, John Wiley
and Sons, Baltimore, Md. (1998), each of which is incorporated
herein by reference. Cells, tissues, biological fluids, proteins
and other samples can be obtained from these organisms and detected
using an apparatus or method set forth herein.
[0125] A template nucleic acid can be obtained from a preparative
method such as genome isolation, genome fragmentation, gene cloning
and/or amplification. The template can be obtained from an
amplification technique such as polymerase chain reaction (PCR),
rolling circle amplification (RCA), multiple displacement
amplification (MDA) or the like. Exemplary methods for isolating,
amplifying and fragmenting nucleic acids to produce templates for
analysis on an array are set forth in U.S. Pat. Nos. 6,355,431 or
9,045,796, each of which is incorporated herein by reference.
Amplification can also be carried out using a method set forth in
Sambrook et al., Molecular Cloning: A Laboratory Manual, 3rd
edition, Cold Spring Harbor Laboratory, New York (2001) or in
Ausubel et al., Current Protocols in Molecular Biology, John Wiley
and Sons, Baltimore, Md. (1998), each of which is incorporated
herein by reference.
[0126] The present disclosure further provides a detection
apparatus that includes (a) a vessel having a lumen and a wall,
wherein the wall has an internal surface and an external surface,
wherein the wall has a plurality of discrete contacts between the
internal surface and the external surface, wherein the internal
surface contacts the lumen, and wherein the plurality of discrete
contacts occupies a length in a scan dimension x; (b) a
transmissive surface; (c) a preload configured to urge discrete
contacts on the external surface of the vessel to contact the
transmissive surface, optionally, the area of the transmissive
surface can have a maximum length in the scan dimension x that is
shorter than length ; (d) a scan actuator configured to slide the
vessel along the transmissive surface in the scan dimension x; and
(e) a detector configured to acquire signals from the discrete
contacts via the transmissive surface.
[0127] As exemplified in several embodiments herein, optical
signals can be relayed to a detection apparatus via transmissive
surface that is transparent to optical signals. An objective serves
as a useful transmitter of optical signals from a vessel to a
detector. In some embodiments the transmitter is an array of
lenses. The lenses in the array can be configured to collect
signals from (or direct energy to) different areas in an xy plane.
The lenses can be arranged to collect signals from contiguous areas
in the xy plane or, alternatively, the areas that are observed can
be separated by interstitial regions that are not observed when the
areas are observed. In some embodiments, the vessel includes an
array of sites that is configured to be observed by an array of
lenses. Each lens can be configured to simultaneously observe one
or more sites in the array of sites. For example, each lens can be
configured to observe at least 1, 4, 9, 16, 25, 36, 49, 64, 81, 100
or more sites in an array of sites. Alternatively or additionally,
each lens can be configured to observe at most 100, 81, 64, 49, 36,
25, 16, 9, 4 or 1 site(s) in an array of sites. Accordingly, an
embodiment is provided wherein each lens is configured to observe a
single site.
[0128] Each lens in an array of lenses can be aligned with its own
optical train to direct radiation to one or more detector.
Alternatively, multiple lenses can be combined into a common
optical train to direct radiation to one or more detector. The
optical trains can include any of a variety of optical components
including, but not limited to, a collimating lens for collimating
signals from the array of sites, a color separating element for
spectrally separating radiation; and a focusing lens for focusing
radiation from the sites to a detector. Exemplary configurations
for an array of lenses and an array of sites observed by the lenses
is provides in U.S. Pat. No. 9,581,550, which is incorporated
herein by reference. For example, the sites of the array can be
zero mode waveguides (ZMWs).
[0129] Other transmitters can be used as appropriate for the energy
or signal that is to be transmitted. For example, a transmissive
surface can conduct electrical signals, thermal signals, magnetic
signals, pressure signals, audio signals, or the like. Temporary
electrical contacts such as pogo pins can be used to transmit
electrical signals between the transmissive surface and vessel. A
transmitter that is present in an apparatus set forth herein can
transmit energy of a variety of forms, including but not limited to
the aforementioned signals.
[0130] In a particular embodiment, the transmissive surface or the
internal surface of the vessel includes an electronic detector such
as a field-effect transistor (FET) or complementary metal oxide
semiconductor (CMOS). Particularly useful electronic detectors
include, for example, those used for nucleic acid sequencing
applications such as those used for detection of protons as set
forth in US Pat. App. Pub. Nos. 2009/0026082 A1; 2009/0127589 A1;
2010/0137143 A1; or 2010/0282617 A1, each of which is incorporated
herein by reference. Also useful are electronic detectors used to
detect optical signals including for example, those set forth in US
Pat. App. Pub. Nos. 2009/0197326 A1; 2015/0293021 A1; 2016/0017416
A1; or 2016/0356715 A1, each of which is incorporated herein by
reference.
[0131] The apparatus and methods of the present disclosure have
been exemplified in the context of use for nucleic acid sequencing
reactions. The apparatus and methods can be used for other
analytical applications as well. Generally, analytical applications
that are carried out in scanning microscopes can be applied to
apparatus and methods of the present disclosure. For example, the
methods or apparatus can be configured to scan microarrays that are
used for analyzing enzyme activity, binding of ligands to
receptors, binding of complementary nucleic acids to each other,
presence of mutations (such as single nucleotide polymorphisms
(SNPs)) in nucleic acids, expression level for RNA species.
Microarrays that are detected via optical labels, such as
fluorophores, are particularly applicable. Larger biological
samples such as cells or tissues can be detected using a method or
apparatus herein. Again, detection modalities that utilize
optically detected probes or stains are particularly applicable.
Other uses include evaluation of manufactured products for which
quality or other characteristics are evaluated via microscopic
scanning. Exemplary products include, but are not limited to,
computer chips, sensors, electronic components and other devices
that are microfabricated or nanofabricated. Tests known in the art
of molecular diagnostics can be modified for use in an apparatus or
method set forth herein such as binding assays (e.g. enzyme-linked
immunosorbent assay (ELISA)), real time polymerase chain reaction
assays and the like.
[0132] Apparatus and methods set forth herein in the context of
detecting reactions can be readily modified for use in preparative
methods. In particular embodiments, the present disclosure provides
reactor apparatus. A reactor apparatus can include (a) a vessel
having a lumen and a wall, wherein the wall has an internal surface
and an external surface, wherein the internal surface contacts the
lumen; (b) a reference surface that forms a structural loop with an
energy source; (c) a preload configured to urge the external
surface of the vessel to contact an area on the reference surface;
(d) a scan actuator configured to slide the vessel along the
reference surface in a scan dimension; and (e) a transmitter
configured to direct energy from the energy source to the internal
surface or the lumen when the external surface of the vessel is
urged by the preload to contact the reference surface.
[0133] Also provided is a method of performing reactions in a
vessel. The method can include (a) translating a vessel along a
reference surface of a reactor apparatus, wherein the vessel
comprises a lumen and a wall, wherein the lumen comprises
reactants, wherein the reference surface contacts at least a
portion of the vessel during the translating, and wherein the
reference surface forms a structural loop with an energy source;
and (b) directing energy from the energy source to the reactants at
different locations along the vessel, wherein the vessel is urged
to the reference surface by a preload during the directing of the
energy to the reactants, thereby performing reactions in the
vessel.
[0134] A method of performing reactions can include (a) delivering
energy from a reactor apparatus to a first subset of reactants in a
vessel while applying a preload to a first portion of the vessel,
wherein the preload positions the first subset of reactants to
occupy an xy plane of a reaction zone, wherein the preload is not
applied to a second portion of the vessel; (b) translating the
vessel to position a second subset of the reactants in the xy plane
of the reaction zone; and (c) delivering energy from the reactor
apparatus to the second subset of the analytes in the vessel while
applying the preload to a second portion of the vessel, wherein the
preload positions the second subset of the analytes to occupy the
xy plane, wherein the preload is not applied to the first portion
of the vessel, thereby performing reactions in the vessel.
[0135] Exemplary energy sources that can be used in apparatus
herein include, but are not limited to, radiation sources such as a
laser, light emitting diode (LED), lamp, microwave source, or x-ray
generator; electricity source; ion beam source such as a
duoplasmitron; electron emitter such as a hot filament or hollow
cathode; electric current source; or voltage source.
[0136] Throughout this application various publications, patents
and/or patent applications have been referenced. The disclosures of
these documents in their entireties are hereby incorporated by
reference in this application.
[0137] The term "comprising" is intended herein to be open-ended,
including not only the recited elements, but further encompassing
any additional elements.
[0138] As used herein, the term "each," when used in reference to a
collection of items, is intended to identify an individual item in
the collection but does not necessarily refer to every item in the
collection. Exceptions can occur if explicit disclosure or context
clearly dictates otherwise.
[0139] A number of embodiments have been described. Nevertheless,
it will be understood that various modifications may be made.
Accordingly, other embodiments are within the scope of the
following claims.
* * * * *