U.S. patent application number 11/566594 was filed with the patent office on 2007-05-31 for imaging of biological samples.
This patent application is currently assigned to REGENTS OF THE UNIVERSITY OF MINNESOTA. Invention is credited to Martin Blumenfeld, Jesse R. Grenz, Mark A. Sanders, Joseph J. Talghader.
Application Number | 20070121111 11/566594 |
Document ID | / |
Family ID | 23722513 |
Filed Date | 2007-05-31 |
United States Patent
Application |
20070121111 |
Kind Code |
A1 |
Blumenfeld; Martin ; et
al. |
May 31, 2007 |
Imaging of Biological Samples
Abstract
A system and method using an electronic light detector array,
e.g., a CCD or a CMOS-based detector array, is used to acquire a
visual image of a biological sample that includes biological
material associated with a biological material holding structure
(e.g., a DNA spot array on a DNA chip, protein bands in a 2-D gel,
etc.). For example, fluorescence from a biological sample may be
detected.
Inventors: |
Blumenfeld; Martin;
(Minneapolis, MN) ; Sanders; Mark A.;
(Minneapolis, MN) ; Talghader; Joseph J.; (Eden
Prairie, MN) ; Grenz; Jesse R.; (Minneapolis,
MN) |
Correspondence
Address: |
FISH & RICHARDSON P.C.
PO BOX 1022
MINNEAPOLIS
MN
55440-1022
US
|
Assignee: |
REGENTS OF THE UNIVERSITY OF
MINNESOTA
|
Family ID: |
23722513 |
Appl. No.: |
11/566594 |
Filed: |
December 4, 2006 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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09852375 |
May 10, 2001 |
7145645 |
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11566594 |
Dec 4, 2006 |
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09434027 |
Nov 4, 1999 |
6784982 |
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11566594 |
Dec 4, 2006 |
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Current U.S.
Class: |
356/318 ;
356/417 |
Current CPC
Class: |
B01J 2219/00529
20130101; G06T 1/0007 20130101; B01J 2219/00702 20130101 |
Class at
Publication: |
356/318 ;
356/417 |
International
Class: |
G01J 3/30 20060101
G01J003/30; G01N 21/25 20060101 G01N021/25 |
Claims
1-115. (canceled)
116. A system for use in detecting a reaction of a biological
sample to light, comprising: a light source and an electronic light
detector defining a light path between the light source and the
light detector; a sampler holder to position a biological sample in
the light path; a fiber optic bundle in the light path to carry the
light along at least a part of the light path.
117. The system of claim 116, wherein the sample holder defines a
plane in which the biological sample is substantially located, with
a first side and an opposed second side to the plane, and wherein
the light source and the electronic light detector are both located
on the first side of the plane.
118. The system of claim 116, wherein the light detector is adapted
to sense light of fluorescence from the biological sample.
119. The system of claim 116, wherein the light source comprises a
laser.
120. The system of claim 116, wherein light in at least a portion
of the light path is coherent light.
121. The system of claim 116, further comprising one or more
filters in the light path to permit passage of light in a
relatively defined wavelength range.
122. The system of claim 121, wherein the filters comprise one or
more polarizing filters.
123. The system of claim 116, further comprising image acquisition
software to assemble individual acquired images into a master image
of all or a portion of the biological sample.
124. The system of claim 116, wherein the fiber optic bundle
comprises a fanout end and a clustered end
125. The system of claim 124, wherein the fiber optic bundle
defines a line at the fanout end.
126. The system of claim 125, wherein the line defines a single
dimension of optical fiber ends.
127. The system of claim 115, wherein the fiber optic bundle forms
an angle between the fanout end and the clustered end
128. The system of claim 127, wherein the clustered end generally
forms a cylinder whose cross section defines a plane that is
parallel with the line defined by the fanout end.
129. The system of claim 127, wherein the fiber optic bundle forms
substantially a right angle between the fanout end and the
clustered end.
130. The system of claim 116, wherein the light source generates
light at a plurality of wavelengths corresponding to markers
associated with the biological sample.
131. The system of claim 116, further comprising a master computer
to coordinate movement of the sample and operation of the light
detector.
132. The system of claim 131, wherein the master computer is
configured to compose a complete image from a plurality of sensed
portions of the biological material.
133. The system of claim 116, further comprising a light collimator
in the light path adjacent the fiber optic bundle.
134. The system of claim 116, further comprising a mapping lens to
focus light onto the electronic light detector.
135. The system of claim 116, wherein the electronic light detector
comprises a linear light detector array.
136. The system of claim 116, further comprising a light-tight
enclosure around the light path.
137. A method of detecting a reaction of a biological sample to
light, comprising: providing a biological sample in a light path
between a light source and an electronic light detector, scanning
the biological sample in the light path; and passing light in the
light path through a optical fiber array to produce one or more
representations of the scanned biological sample on the electronic
light detector.
138. The system of claim 137, wherein the step of scanning the
biological sample in the light path comprises scanning the optical
fiber array across the biological sample.
139. The system of claim 137, wherein scanning the optical fiber
array across the biological sample comprises translating the
biological sample past the optical fiber array.
140. The system of claim 137, wherein the optical fiber array
comprises a first fanout end and a second clustered end, and
wherein the first fanout end is positioned close to the biological
sample.
141. The system of claim 137, wherein the step of scanning the
biological sample in the light path comprises linearly translating
the sample.
142. The system of claim 137, further comprising capturing the
light with an electronic light detector.
143. The system of claim 142, further comprising providing a
fluorescent tag on a part of the biological sample so that the tag
excites and is detected by the electronic light detector when light
impinges on the part of the biological sample.
144. The system of claim 143, wherein the fluorescent tag comprises
a label on a piece of DNA that is complementary with other DNA in
the biological sample.
145. The system of claim 137, wherein the light is generated via
fluorescence.
146. The system of claim 137, further comprising rastering a laser
across the biological sample.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS(S)
[0001] This application is a continuation-in-part of U.S. patent
application Ser. No. 09/434,027, filed on Nov. 4, 1999, which is
incorporated herein by reference.
FIELD OF THE INVENTION
[0002] The present invention pertains to imaging systems and
methods. More particularly, the present invention relates to
imaging and/or mapping of biological samples using electronic light
detectors.
BACKGROUND OF THE INVENTION
[0003] Various conventional approaches have been used to visualize
the surface of a biological sample, e.g., DNA spots of a
micro-array such as a DNA chip, protein bands in a one dimensional
(1-D) or two dimensional (2-D) gel, etc. For example, a DNA chip is
generally a rigid flat surface, typically glass or silicon, that
may have short chains of related nucleic acids spotted, e.g., DNA
spots, in rows and columns, i.e., an array, thereon. Hybridization
between a fluorescently-labeled DNA and specific locations on the
chip can be detected and analyzed by computer-based
instrumentation. The information derived from the results of
hybridization to DNA chips is stimulating advances in drug
development, gene discovery, gene therapy, gene expression, genetic
counseling, and plant biotechnology.
[0004] Among the technologies for creating DNA chips are
photolithography, "on-chip" synthesis, piezoelectric printing, and
direct printing. Chip dimensions, the number of sites of DNA
deposition (sometimes termed "addresses") per chip, and the width
of the DNA spot per "address" are dependent upon the technologies
employed for deposition. The most commonly used technologies
produce spots with diameters of 50-300 .mu.m. Photolithography
produces spots that can have diameters as small as, for example, 1
micron. Technologies for making such chips are known to those
skilled in the art and are described, for instance, in U.S. Pat.
Nos. 5,925,525; 5,919,523; 5,837,832; and 5,744,305; which are all
incorporated herein by reference.
[0005] Hybridization to DNA chips can be monitored by fluorescence
optics, by radioisotope detection, and by mass spectrometry. The
most widely-used method for detection of hybridization employs
fluorescently-labeled DNA, and a computerized system featuring a
confocal fluorescence microscope (or an epifluorescence
microscope), a movable microscope stage, and DNA detection
software. Technical characteristics of these microscope systems are
described in U.S. Pat. Nos. 5,293,563; 5,459,325; and 5,552,928,
which are all incorporated herein by reference. Further
descriptions of imaging fluorescently immobilized biomolecules and
analysis of the images are set forth in U.S. Pat. Nos. 5,874,219;
5,871,628; 5,834,758; 5,631,734; 5,578,832; 5,552,322; and
5,556,529, which are all incorporated herein by reference.
[0006] In brief, these conventional approaches to visualizing the
surface of a DNA chip involve placing the chip on a stage of a
microscope, moving the stage to put the sample into focus with a
microscope objective, and triggering a digital camera or similar
device to capture an image. The microscope objective is generally a
device made of a group of lenses that have a sophisticated design
that collects light from the sample, magnifies the image of the
sample, and minimizes the unavoidable image and color distortion
caused by the passage of the light through the objective. The light
collected from the sample may pass through the microscope objective
and through a set of mirrors and lenses until it is delivered to an
eyepiece or the camera. The light path is the path that the light
takes from the point where it leaves the surface of the sample
until it reaches an imaging device such as an eyepiece or camera.
The microscope generally is associated with a light source that
directs light onto the sample.
[0007] These microscopes also generally have sets of optical
filters that allow for viewing of fluorescent images. For example,
the DNA that is hybridized to the surface of the DNA chip is
typically labeled with fluorescent molecules that absorb light at
one wavelength and then emit a different wavelength. The microscope
may be equipped with sets of optical filters that block the
wavelengths of light from the light source associated with the
microscope but which allow the light emitted by the fluorescent
molecules to pass therethrough such that the light may reach the
eyepiece or camera. The light source is typically integral with the
microscope and is an important part of the imaging system.
[0008] Further, generally, 1-D and 2-D electrophoresis processes
are electrophoretic methods for resolving complex mixtures of
proteins, e.g., 2-D electrophoresis is a multiple step process for
resolving complex mixtures of proteins. For example, in 2-D
electrophoresis, the proteins in a sample may first be dissociated
into polypeptide subunits by dissolving in an appropriate buffer.
The sample may then be applied to the top of a tube gel containing
ampholines. Isoelectric focusing (IEF) is then carried out in the
first dimension. After the IEF is carried out, the gel which
contains the peptides is removed from the gel tube and placed over
a slab gel and sealed by overlapping stacking gel; and thereafter,
the second dimension of slab gel electrophoresis is carried out
(e.g., proteins (negatively charged) run from the top of the slab
(held at a negative charge) toward the bottom of the slab (held at
a positive charge). Then, staining, e.g., using a stain that binds
to proteins so they can be identified, and an optional drying step,
is carried out. Thus, the polypeptides are separated according to
the independent parameters of isoelectric point in the first
dimension and molecular weight in the second dimension (e.g.,
protein bands). For example, a large number, e.g., 1000,
polypeptide spots (e.g., protein bands) may be resolved on a single
two dimensional gel. Further, for example, such proteins in a 2-D
gel may be labeled with fluorescent or chemi-luminescent
markers.
[0009] Such protein bands in 1-D and 2-D electrophoresis may also
be visualized and analyzed. Like DNA chips, such visualization of
the protein bands in the 2-D gel is generally performed using the
same conventional approaches as used to visualize the surface of a
DNA chip, e.g., a microscope with the sample put into focus using a
microscope objective, a digital camera, etc.
[0010] These conventional microscopes are sophisticated and
expensive instruments that require training and maintenance. A
single microscope objective typically has multiple lenses that are
generally very expensive. A lens generally refers to a transparent
solid material shaped to magnify, reduce, or redirect light rays,
e.g., focus light. A light filter or mirror is distinct from a
lens. Furthermore, use of a microscope requires a dedicated
workspace that is approximately the size of a typical desk.
Conventional microscopes have a light path that is several
centimeters long that transmits collected light through air and
other assorted optical devices within the light path. One of the
challenges in microscopy is making the microscope as efficient as
possible in capturing all of the light that leaves the sample
surface so that an optimal image can be captured.
[0011] This costly instrumentation conventionally used to image
biological samples, e.g., DNA chips, impedes the broad usage of
such technologies. Therefore, an inexpensive, low-maintenance
alternative spot detection method and apparatus for biological
sample analysis, e.g., DNA chip analysis, that is easy to use and
requires a minimum of space and maintenance is needed.
[0012] Integrated electronic circuit arrays for light-detection
(e.g., a member of a group of detectors referred to as electronic
light detectors) are readily available. They generally are based on
CCD (charge-coupled device) or CMOS (complementary metal oxide
semiconductor) technologies. Both CCD and CMOS image detectors are
generally two-dimensional arrays of electronic light sensors,
although linear imaging detectors (e.g., linear CCD detectors) that
include a single line of detector pixels or light sensors, such as,
for example, those used for scanning images, are also available.
Each array includes a set of known, unique positions that may be
referred to as having addresses. Each address in a CCD or CMOS
detector is occupied by a sensor that covers an area (e.g., an area
typically shaped as a box or a rectangle). This area occupied by a
single sensor is generally referred to as a pixel or pixel area. As
used herein, a light-detecting sensor located in a pixel area is
referred to as a detector pixel. A detector pixel, as generally
used herein, may be a CCD sensor, a CMOS sensor, or any other
device or sensor that detects or measures light. The sizes of
detector pixels vary widely and may have a diameter or length of
0.2 .mu.m, which is also the theoretical limit of resolution of a
light microscope. It is noted that some detectors have resolving
sizes lower than 0.2 .mu.m, such as for use in microscopes
employing light of wavelengths of 180 nm and below.
[0013] CCD detectors, widely used in consumer and scientific
applications such as digital recorders and digital cameras, are
sensitive, and may be made with detector pixels that are smaller
than those of CMOS devices. CMOS devices are now beginning to be
incorporated in recorders and cameras because they are less
expensive to produce. CMOS devices also are easier to interface
with external control systems than CCD detectors. Some
readily-available CMOS devices are integrated with the capabilities
to provide acquiring, digitizing, and transmitting an image without
additional circuitry, while CCD detectors generally require
additional circuit elements to accomplish the same tasks.
SUMMARY OF THE INVENTION
[0014] A system for use in detecting biological material of a
biological sample according to the present invention includes a
positioning apparatus for providing a biological sample in a
sampling position. The biological sample (e.g., a micro-array or a
gel) includes biological material associated with a biological
material holding structure with the biological material holding
structure having first and second opposing sides. The system
further includes an electronic light detector array with the
electronic light detector array including a plurality of detector
pixels located at particular detector pixel addresses. The
plurality of detector pixels face the first side of the biological
sample to receive light therefrom. A light source is operable to
provide source light. The sampling position is a position that
places the biological sample in a defined spatial relationship
relative to the electronic light detector array such that the
source light impinges on at least one portion of the first side of
the biological material holding structure of the biological sample,
and further such that, in response to such impinging light, light
representative of the biological sample is provided via a light
path for detection by one or more of the detector pixels. Control
circuitry is operable to acquire at least one frame of image data
representative of biological material of the biological sample
using the plurality of detector pixels to detect the light
representative of the biological sample provided via the light
path.
[0015] In one embodiment, the control circuitry is operable to
acquire a plurality of frames of image data representative of
biological material of the biological sample using the plurality of
detector pixels. Further, the control circuitry may be operable to
provide an image for display using the plurality of frames of image
data.
[0016] In another embodiment of the system, the light source
provides an excitation light that impinges on the at least one
portion of the biological material holding structure of the
biological sample, and further such that, in response to such
excitation light, fluorescence representative of biological
material of the biological sample is provided via the light path
for detection by one or more of the plurality of detector pixels.
The control circuitry is operable to acquire at least one frame of
image data representative of detected fluorescence. In various
further embodiments, the light path of the fluorescence to one or
more of the detector pixels may not include any portion of the
biological material holding structure, the system may further
include an emission light filter positioned between the biological
sample and the plurality of detector pixels operable to prevent
excitation light from impinging on the plurality of detector
pixels, the system may further include a focusing lens positioned
between the biological sample and the plurality of detector pixels
operable to focus the fluorescence onto one or more of the
plurality of detector pixels, and the biological material holding
structure may be formed of an opaque material.
[0017] In another embodiment of the system, in response to the
impinging light, reflected light representative of the biological
sample is provided via the light path for detection by one or more
of the plurality of detector pixels. The control circuitry is
operable to acquire at least one frame of image data representative
of detected reflected light. In various other embodiments thereof,
the system may further include a focusing lens positioned between
the biological sample and the plurality of detector pixels operable
to focus the reflected light onto one or more of the plurality of
detector pixels, and further, the biological holding material
structure may be formed of an opaque material.
[0018] A polynucleic acid micro-array according to the present
invention is also described. The micro-array includes a biological
material holding structure having a sample surface and an opposing
surface joined to the sample surface by a body portion. The sample
surface has immobilized nucleic acid sequences thereon and further,
the biological material holding structure is made of an opaque
material.
[0019] A method for use in detecting biological material according
to the present invention includes providing a biological sample in
a sampling position. The biological sample includes biological
material associated with a biological material holding structure
with the biological holding structure having first and second
opposing sides. The method further includes positioning an imaging
device in proximity to the biological sample with the imaging
device having an electronic light detector array. The electronic
light detector array includes a plurality of detector pixels
located at particular detector pixel addresses and positioned such
that the plurality of detector pixels are facing the first side of
the biological sample. A source light is provided to impinge on at
least a portion of the first side of the biological material
holding structure of the biological sample such that, in response
to such impinging light, light representative of the biological
sample is provided via a light path for detection by one or more of
the detector pixels. At least one frame of image data
representative of biological material of the biological sample is
acquired using the plurality of detector pixels to detect the light
representative of the biological sample provided via the light
path.
[0020] In one embodiment of the method, the source light may be an
excitation light that impinges on the at least one portion of the
first side of the biological material holding structure of the
biological sample such that, in response to the excitation light,
fluorescence representative of biological material of the
biological sample is provided via the light path for detection by
one or more of the plurality of detector pixels.
[0021] In a further embodiment of the method, in response to the
impinging light, reflected light representative of the biological
sample is provided via the light path for detection by one or more
of the plurality of detector pixels.
[0022] Another system for detecting a pattern of polynucleic acid
hybridization to a surface according to the present invention
includes positioning structure to provide a polynucleic acid chip
at a sampling position with the polynucleic acid chip including a
sample surface and an opposing surface. The sample surface has one
or more sequences of polynucleic acids immobilized thereto with
each sequence being immobilized to a particular chip address. The
system further includes an electronic light detector array that
includes detector pixels located at particular detector pixel
addresses. A light source provides source light. The sampling
position is a position that places the sample surface of the
polynucleic acid chip in a defined spatial relationship relative to
the electronic light detector array such that the source light
impinging on at least one chip address on the sample surface is
substantially directed onto at least one detector pixel with a
detector pixel address that is correlated to the at least one chip
address.
[0023] In various embodiments of the system, light from the sample
surface of the polynucleic acid chip passes through a thickness of
the polynucleic acid chip before reaching the detector pixels, the
polynucleic acid chip is formed of a light-transmissive material,
the system may further include an optical filter that selectively
transmits light (e.g., an optical filter located between the sample
surface and the detector pixels), the system may further include a
mapping lens that changes the direction of light rays leaving the
sample surface of the polynucleic acid chip (e.g., a mapping lens
located between the sample surface and the detector pixels), the
polynucleic acid chip may be in direct physical contact with the
filter (e.g., either the opposing surface or the sample surface),
the filter and the detector pixels of the detector array may be
direct physical contact, or the polynucleic acid chip and the
electronic light detector array may be in direct physical contact
(e.g., either the opposing surface or the sample surface).
[0024] A polynucleic acid chip according to the present invention
is also described. The chip includes a sample surface that has
immobilized polynucleic acid sequences attached thereto and an
opposed surface. The chip is formed of a light transmitting
material.
[0025] In various embodiments of the chips, the chip may include an
optical filter (e.g., an optical coating on the opposed surface of
the chip) and/or the chip may include an optical lens.
[0026] Further, in another embodiment of an imaging system
according to the present invention, a fiber optic bundle light
source apparatus is used in conjunction with an electronic light
detector to perform imaging of a biological sample. For example,
the fiber optic bundle light source apparatus may receive light
from a cluster of LEDs and is terminated at a linear array of
fibers that is scanned across the biological sample. The electronic
light detector includes detector pixels that detect light
representative of linear portions of the biological sample. Such
linear portions may be combined to form an image of at least a
portion of the biological sample.
[0027] The above summary of the present invention is not intended
to describe each embodiment or every implementation of the present
invention. Advantages, together with a more complete understanding
of the invention, will become apparent and appreciated by referring
to the following detailed description and claims taken in
conjunction with the accompanying drawings.
BRIEF DESCRIPTION OF THE DRAWINGS
[0028] FIG. 1 illustrates the components and general function of an
electronic light detector array system according to the present
invention for imaging a biological sample;
[0029] FIG. 2 illustrates the use of direct mapping to acquire and
reconstruct light representative of DNA spots of a DNA chip in an
electronic light detector array detection system such as that shown
in FIG. 1;
[0030] FIGS. 3A and 3B illustrate two alternative arrangements of
optical components for direct mapping in an electronic light
detector array detection system according to the present
invention;
[0031] FIG. 4 is a block diagram of an alternate embodiment of an
electronic light detector array detection system according to the
present invention;
[0032] FIG. 5 illustrates an embodiment of an electronic light
detector array detection system according to the present invention
with a laser-light source;
[0033] FIG. 6 illustrates an embodiment of an electronic light
detector array detection system according to the present invention
with a dichroic mirror;
[0034] FIG. 7 illustrates an embodiment of an electronic light
detector array detection system according to the present invention
with a dichroic mirror and a mapping lens;
[0035] FIG. 8A illustrates a DNA chip with hybridized DNA to be
mapped using an electronic light detector array detection system
according to the present invention;
[0036] FIG. 8B illustrates an embodiment of an electronic light
detector array detection system according to the present invention
with no optical filter;
[0037] FIG. 8C illustrates an embodiment of an electronic light
detector array detection system according to the present invention
with a cover and no optical filter;
[0038] FIG. 9A illustrates an embodiment of an electronic light
detector array detection system according to the present invention
with a combination mapping lens-filter;
[0039] FIG. 9B illustrates an embodiment of an electronic light
detector array detection system according to the present invention
with a combination chip-filter;
[0040] FIG. 10 shows another alternate embodiment of an image
detection apparatus according to the present invention;
[0041] FIGS. 11A-11C provide an illustrative exemplary and more
detailed configuration of the image detection apparatus generally
shown in FIG. 10;
[0042] FIG. 12 shows an illustrative diagram of another alternate
electronic light detector array detection system according to the
present invention;
[0043] FIG. 13 shows one illustrative exemplary and more detailed
configuration of the image detection apparatus of the system
generally shown in FIG. 12; and
[0044] FIG. 14 shows another alternate illustrative exemplary and
more detailed configuration of the image detection apparatus of the
system generally shown in FIG. 12.
DETAILED DESCRIPTION OF THE EMBODIMENTS
[0045] The present invention provides inexpensive devices and
methods for resolving light (e.g., emitted light by fluorescent
labeled nucleic acid spots) representative of biological samples
(e.g., nucleic acid spots on a micro-array such as a DNA chip,
protein bands of a 1-D or 2-D gel, etc.) for the detection thereof.
As used herein, biological samples refers to biological material
(proteins, nucleic acids, tissues, etc.) associated with a
biological material holding structure (e.g., a micro-array
substrate such as a DNA chip substrate a gel, etc.) in a manner
that allows for detection of the biological material, or portions
thereof (e.g., with the use of markers such as dyes, tags, labels,
or stains), such as through the use of imaging (e.g., direct
mapping).
[0046] The term, "biological samples" refers not only to the
biological material itself (proteins, nucleic acids, tissues, etc.)
but also to other materials associated therewith used for detection
of the biological material, or portions thereof (e.g., dyes,
labels, stains, or any other marker used in the identification of
materials). As used herein, biological material refers to, for
example, a sample of tissue or fluid isolated from a subject,
including but not limited to, for example, blood, plasma, serum,
fecal matter, urine, bone marrow, bile, spinal fluid, lymph tissue
and lymph fluid, samples of the skin, external secretions of the
skin, respiratory, intestinal, and genitourinary tracts, tears,
saliva, milk, blood cells, organs, biopsies and also samples of in
vitro cell culture constituents including but not limited to
conditioned media resulting from the growth of cells and tissues in
culture medium, e.g., recombinant cells, and cell components. A
biological sample can include, for instance, a polypeptide or a
polynucleotide.
[0047] "Polypeptide" as used herein refers to a polymer of amino
acids and does not refer to a specific length of a polymer of amino
acids. Thus, for example, the terms peptide, oligopeptide protein,
and enzyme are included within the definition of polypeptide. This
term also includes post-expression modifications of the
polypeptide, for example, glycosylations, acetylations,
phosphorylations and the like.
[0048] Also, as used herein, the term "polynucleotide" refers to a
polymeric form of nucleotides of any length, either ribonucleotides
or deoxynucleotides, and includes both double- and single-stranded
DNA and RNA. A polynucleotide may include nucleotide sequences
having different functions, including for instance coding
sequences, and non-coding sequences such as regulatory sequences. A
polynucleotide can be obtained directly from a natural source, or
can be prepared with the aid of recombinant, enzymatic, or chemical
techniques. A polynucleotide can be linear or circular in topology.
A polynucleotide can be, for example, a portion of a vector, such
as an expression or cloning vector, or a fragment.
[0049] One or more embodiments of the present invention are
operable for use in multiple imaging applications, e.g., imaging of
two-dimensional and three-dimensional objects, such as fluorescence
imaging, reflective imaging, bar code imaging, densitometry, gel
documentation, or in any other application wherein imaging of a
biological sample is beneficial. One or more of the systems and
methods as described herein may be used for ultra-sensitive sample
detection. One or more of the imaging systems and methods of the
present invention are flexible (e.g., can image various objects and
perform various types of imaging such as fluorescence and
reflective imaging) light imaging systems with the ability to
produce high-quality images from, for example, various biological
sample configurations that use, for example, single color
fluorescence, multiple color fluorescence, chemi-luminescence,
chemi-fluorescence, calorimetric detection, densitometry, or any
other technique detectable through imaging. Such image quality,
e.g., spatial resolution, is dependant, at least in part, on the
lens and electronic light detector used in such systems. Such
imaging provides the ability for filmless detection.
[0050] At least some of the imaging systems and methods of the
present invention provide for the rapid production of single-color
and multi-color fluorescence images, e.g., images showing
fluorescent positions such as regions, spots, areas, etc., of a
biological sample (e.g., fluorescent positions on a micro-array or
DNA chip) when such material is caused to fluoresce by a light
source. A wide range of samples, including, but not limited to
gels, blots, micro-arrays, micro-plates, etc. may be imaged to
detect fluorescent positions. Such methods and systems have a high
sensitivity for detection of fluorescent dyes and labels,
including, but clearly not limited to, ethidium bromide, SYBR.RTM.
Green, SYBR.RTM. Gold, SYPRO.RTM., Radiant Red, fluorescein (FITC),
rhodamine, Cy2, Cy3, Texas Red, Green Fluorescent Protein
(GFP).
[0051] With regard to chemi-luminescence imaging, light emitted by
biological samples is detected using one or more imaging systems
and methods of the present invention. For example, horse radish
peroxidase (HRP) and alkaline phosphatase (AP) activated biological
samples may be detected with suitable quality and accurate
quantitation. Further, for example, high sensitivity detection of,
for example, proteins, using enhanced chemi-luminescence (ECL),
e.g., detection of western dot blots and chemi-fluorescent
substrates such as AttoPhos and ECL-Plus, may be attained. Further,
with respect to densitometry and calorimetric imaging, various
calorimetric stains, including, but clearly not limited to,
Coomassie Blue, copper, zinc, and silver stain may be detected.
[0052] Portions of the following description is primarily provided,
for simplicity, with reference to use of micro-arrays such as DNA
chips. However, one skilled in the art will recognize that the
present invention is applicable to any imageable biological sample,
e.g., 1-D gels, 2-D gels, blots, substrates having biological
material thereon. For example, as previously noted, such systems
and/or methods may be used to image two-dimensional gels, e.g.,
fluorescent labeled protein bands of such gels. Thus, polypeptides
separated according to the independent parameters of isoelectric
point and molecular weight (e.g., protein bands) can be imaged
using the present invention.
[0053] The smallest diameter DNA spot generally attainable on a
micro-array, e.g., a DNA chip, approximates the diameter or length
of a detector pixel, e.g., about 10 .mu.m, of a conventional
electronic light detector array, e.g., CMOS light detector array.
Therefore, if the DNA array on the DNA chip and the detector pixels
of the electronic light detector, e.g., CMOS light detector array,
are in close proximity to each other, the light emitted by each
spot of a DNA array can be directly mapped to a limited number of
detector pixels in the electronic light detector array. Such direct
mapping would eliminate the expensive optical systems that are
conventionally required for DNA chip analysis, and, by lowering the
cost, expand the potential applications of DNA chip technology.
[0054] For example, one embodiment of a system and/or method
according to the present invention may include direct mapping of
light emitted by a single DNA spot onto one or more corresponding
detector pixels of an electronic light detector array. Further, for
example, one embodiment of a system and/or method may position the
DNA chip in direct physical contact with an electronic light
detector array. In a modification of such systems/or methods, a
simple optical system, such as a single mapping lens, may be used
to map an enlarged or reduced version of the DNA spot array onto an
electronic light detector array. Further, for example, a modified
bar code reader may be used to image a biological sample for
detection of biological material thereof, or portions of such
biological material. As described further below, computer software
is used to process the data from the electronic light detector
array system. For example, the data may be treated as a
two-dimensional map, or otherwise processed as an array of
data.
[0055] An imaging system according to the present invention may be
used to replace expensive optical detection systems currently
employed for DNA chip analysis. In general, one embodiment of such
a system may include an electronic light detector array, a filter,
and, optionally, a mapping lens apparatus that enables a DNA chip
having an array of DNA spots to be mapped onto the electronic light
detector array. For example, each position on the DNA chip surface
has a corresponding position or set of positions, i.e., detector
pixels, on the electronic light detector array. Light associated
with the array of DNA spots, e.g., fluorescence, at an address on
the DNA chip surface is received or sensed at one or more known
addressed detector pixels or set of detector pixels.
[0056] Such imaging, e.g, mapping of biological sample information
to detector pixels, is inexpensive. It eliminates the need for a
complicated microscope that requires maintenance and trained
personnel. It may capture light directly from a DNA sample. By
eliminating many lenses, the disadvantages stemming from use of
many lenses are reduced. Further, such mapping may enable direct
capture of light so that a maximal amount of light is captured from
the sample. Such minimization of the loss of light creates a
sensitive imaging system.
[0057] Electronic light detector direct mapping may be considered
analogous to the established photographic method known as contact
printing. In contact printing, a photographic negative is placed in
direct contact with unexposed photographic paper, and illuminated
briefly. When the photographic paper is subsequently developed, its
image has a 1:1 correspondence to the negative.
[0058] FIG. 1 generally illustrates components of and the general
function of an electronic light detector array detection system 1,
e.g., a CMOS-based detector array system, which is used to acquire
a visual image 2 of a biological sample that includes biological
material associated with a biological material holding structure
(e.g., a DNA spot array on a DNA chip, protein bands in a 2-D gel,
etc.), reconstruct the image, and display a reconstructed visual
image 12. Such image data may then be analyzed as desired, either
manually or by appropriate software operable upon such image
data.
[0059] For example, when examining and analyzing DNA arrays on
chips, similarities and/or differences between portions of the
array and/or similarities and/or differences between arrays of
multiple chips may be noted. In other words, for example, using the
images provided herein, a user, e.g., a human or a machine, may
note certain biological material or spots that are alike when they
are conditioned in the same way, or pick out spots that are
different than the majority of the other spots of the array.
Further, for example, the user may compare two or more arrays to
see if they are similar or the same. e.g., 90% the same, identical,
etc. Similar examination and analysis may occur for other types of
biological samples.
[0060] The electronic light detector array detection system 1
includes an image detection apparatus 101 that senses light
representative of the visual image 2 using detector pixels, e.g.,
CMOS detector pixels 5, of an electronic light detector 4, e.g., a
CMOS detector array. The image detection apparatus 101 provides
electrical signals generated upon detection of such light
representative of image data in a useable form to a computer 8 of
the system 1, such as via a communications cable 9.
[0061] An electronic light detector, as used herein, may be any
suitable electronic circuit array operable for light-detection.
Generally, such detectors 4 are based on CCD (charge-coupled
device) or CMOS (complementary metal oxide semiconductor)
technologies. Both CCD and CMOS image detectors are generally
two-dimensional arrays of electronic light sensors, although linear
imaging detectors (e.g., linear CCD detectors) that include a
single line of detector pixels or light sensors, such as, for
example, those used for scanning images, may also be suitable
depending on the embodiment described herein. Each array includes a
set of known, unique positions that may be referred to as having
addresses. Each address in a CCD or CMOS detector is occupied by a
sensor that covers an area (e.g., an area typically shaped as a box
or a rectangle). This area occupied by a single sensor is generally
referred to as a pixel or pixel area. As used herein, a
light-detecting sensor located in a pixel area is referred to as a
detector pixel. A detector pixel, as previously described herein,
may be a CCD sensor, a CMOS sensor, or any other device or sensor
that detects or measures light. The sizes of detector pixels vary
widely and may have a diameter or length of 0.2 .mu.m, which is the
theoretical limit of resolution of a light microscope. Light, as
used herein, refers to any electromagnetic emission of at least 120
nm wavelength and includes ultraviolet, visible, and infrared
light.
[0062] Various other associated equipment or components may be
found in association with electronic light detectors, and are known
to those skilled in the art. For example, such equipment may
include manual or electric filter-switchers, movable mirrors, and
motors and controls to raster a laser across a sample. Further, for
example, various equipment or components are associated with CCD
and CMOS sensors, which are incorporated into a myriad of
commercially available cameras and detectors. For instance, various
equipment and techniques are known for producing a color image
using red, green, and blue (e.g., magenta, green, and cyan)
detection. For example, an image may be split into three images,
each of which is sent through a red, green, or blue filter to a CCD
sensor or CCD sensors may be placed on a chip with different
sensitivities to red, green, and blue light. Such equipment
components include techniques (e.g., software processes or
algorithms) and electronic circuitry for improving an image, and
may include, for example, electronic filters (high-pass, low-pass,
etc.), time and frame-averaging, image subtraction, and other
techniques known to those skilled in the art.
[0063] In the computer 8, the image data is stored, e.g., addressed
or mapped, in, for example, the computer's video memory 108. The
image data may be processed to provide data representative of a
reconstructed image 12 which may be provided, e.g., passed by a
cable 10, for display on a monitor 11, e.g., a computer display or
any other display apparatus that may display image data
representative of the reconstructed image 12.
[0064] As shown in FIG. 1, in one illustrative embodiment of the
image detection apparatus 101, light representative of the visual
image 2 is collected by a mapping lens 3 of the illustrative image
detection apparatus 101, which focuses the light representative of
the visual image 2 onto detector pixels 5, e.g., CMOS detector
pixels or CCD detector pixels, of a detector 4, e.g., a CMOS
detector array, a CCD array, or any other light detecting device
having detector pixels to which light from the biological sample
can be mapped. The light may be any type of light representative of
the biological sample, e.g., luminescence from the sample,
fluorescence from the sample. etc. The electronic light detector
array or detector 4 contains a plurality of detector pixels 5. The
detector array or detector 4 is positioned and/or mounted on a
substrate or circuit board 6, which is associated with and/or
contains a power supply 7, e.g., a direct current power supply, for
the detector 4.
[0065] The detector array or detector 4 may have electronic
circuitry 104 associated therewith or may include electronic
circuitry, e.g. analog to digital conversion circuitry, buffer
circuitry, amplification circuitry, etc., that converts electrical
signals generated upon detection of light by the detector pixels 5
to useable form by computer 8, e.g., digital form. Such electronic
circuitry, e.g., circuitry 104, may be used to facilitate the
transfer of the digitized signal representative of the sensed light
to the computer 8 via the communications cable 9. In the computer
8, the digital signal is stored as image data, e.g., addressed or
mapped, to the computer's video memory 108. The image data is
processed to provide data representative of a reconstructed image
12 which may be provided e.g., passed by the cable 10, for display
on monitor 11, e.g., a computer display or any other display
apparatus that may display image data representative of the
reconstructed image 12.
[0066] The electronic light detector 4 may be used in various
configurations to image biological samples for the detection of
biological material, or portions thereof, associated with holding
structure of the biological sample (e.g., holding structure such as
gels, DNA chip substrates, microtiter plates, etc.). Generally,
such configurations fall into two broad categories: transmissive
imaging and reflective imaging.
[0067] As used herein, transmissive imaging configurations refer to
configurations that provide for detection of light from a
biological sample, e.g., from the sample surface at which
biological material is associated, which requires the use of
transmitted light through all, or at least a major portion of, the
biological holding structure, e.g., DNA chip substrate, micro-titer
plates, gels that may be associated with a substrate or imaged
alone, etc. For example, the transmitted light may be an excitation
light that travels through the biological material holding
structure to excite biological material (e.g., tags thereof) which
then emits light that travels in a light path (which as defined
herein refers to the path light travels from the point where it
leaves the biological sample until it reaches the electronic light
detector) and impinges on one or more detector pixels.
Alternatively, the transmitted light may be fluorescence emitted by
biological material (e.g., biological material excited by an
excitation light source) that travels through the biological
holding structure (e.g., the biological material holding structure
is part of the light path) prior to impinging on the one or more
detector pixels.
[0068] In other words, for the electronic light detector 4 to
detect light from the biological sample, light (whether excitation
or fluorescence) is passed through the biological material holding
structure of the biological sample. In such cases, the biological
material holding structure must be light transparent structure,
e.g., glass, clear materials, or other materials that permit
transmission of suitable or desirable wavelengths of light. For
example, such configurations are shown in FIGS. 2-5 and 8-11.
[0069] On the other hand, as used herein, reflective imaging
configurations generally, although not always, refer to
configurations that provide for detection of light from a
biological sample, e.g., a sample surface at which biological
material is associated which does not require the use of
transmitted light through the biological material holding
structure, or a major portion thereof, e.g., DNA chip substrate,
micro-titer plates, gels that may be associated with a substrate or
imaged alone, etc. For example, light reflected from a biological
sample may travel in a light path that does not include the
biological material holding structure. However, such configurations
can be used when light is transmitted through all or a part of the
biological material holding structure. For example, such
configurations may provide for detection of light from a sample
surface at which biological material is associated which requires
the use of transmitted light through all, or at least a major
portion of, the biological holding structure.
[0070] In other words, for the electronic light detector 4 to
detect light in a reflective imaging configuration from the
biological sample, light (whether excitation or fluorescence) may
or need not pass through the biological holding structure of the
biological sample. Preferably, light does not pass through the
biological material holding structure or at least does not pass
through a major portion thereof. As used herein, a major portion
refers to a portion greater than 50 percent, e.g., 50 percent of
the thickness of the substrate. In such cases, the biological
holding structure need not be light transparent structure, but
rather can be opaque materials, e.g., nitrocellulose, charged
nylon, silicon as a substrate for micro-array formation, etc.,
which have more favorable properties than light transparent
structure (e.g., glass). Such reflective imaging configurations are
shown in FIGS. 6-7 and 12-14, where, for example, excitation light
excites fluorescent markers of biological material and is reflected
from a sample surface along with fluorescence being provided via a
light path from the biological sample to the electronic light
detector, or, further, for example, where illumination light is
reflected from the biological sample via a light path to detector
pixels representative of at least absorption characteristics of the
biological sample.
[0071] In many cases, but clearly not in all cases, in the
transmissive imaging configurations involving DNA chips, the
detector pixels of the electronic light detector are facing an
opposing side of a biological material holding structure, e.g., DNA
chip substrate. The opposing side is a side opposite of the sample
surface upon which biological material is provided. However, the
opposing side and the detector pixels are not necessarily directly
in contact or directly facing each other as they may be separated
by filters, lenses, etc.)
[0072] Preferably, in many cases, according to the present
invention, the detector pixels of the electronic light detector in
a reflective imaging configuration (e.g., involving DNA chips) are
facing the sample surface upon which biological material is
provided. However, the sample surface and the detector pixels are
not necessarily directly in contact with one another or directly
facing one another as filters, and lenses may be located
therebetween.
[0073] As used herein, surfaces and/or portions of components that
are facing one another are not necessarily directly facing each
other, e.g., other elements such as filters, lenses, etc. may
separate such surfaces and/or portions of components. Further, as
used herein, directly facing refers to surfaces and/or portions of
components that are immediately next to one another but not
necessarily in direct contact. Further, preferably, although not
necessarily, facing surfaces and/or portions of components (e.g.,
detector pixels arrays) are parallel to one another.
[0074] FIG. 2 illustrates an exemplary embodiment of an image
detection apparatus 101 used in a system to acquire and display an
image 13 representative of sensed light associated with a
biological sample 14, e.g., light emitted by a DNA chip 14 that is
excited with ultraviolet or blue light 105 provided by a light
source 15. A clamping system 19 holds the DNA chip 14, the
electronic light detector array 4, and an optical filter 17 in
contact with each other and in a sampling position.
[0075] In one embodiment of the image detection apparatus 101, the
DNA chip 14 is loaded into the holding structure, e.g., clamping
system 19 or any other type of holder, and the holder is then moved
from a loading position into the sampling position. For example, a
sliding mechanism may be used to slide the holder from the loading
position into the sampling position. Further, any other electrical
and mechanical structure may be used to perform such movement
features, e.g., a motor may be used to move the DNA chip 14. For
example, with the DNA chip loaded into the holder in a loading
position, a switch may be activated to turn a motor on so as to
slide the holder to the sampling position. It will be recognized
that such loading and positioning structure and methods may be used
for any of the embodiments described herein.
[0076] Further, it will be recognized that to focus the image, the
holder may be moved to multiple sampling positions until a sampling
distance desired by a user is achieved, e.g., an image is focused.
For example, the electronic light detector along with any detection
software or imaging software may be used along with, for example, a
graphic display, to visualize the sample surface and the holder or
part of the imaging apparatus may be moved to focus the image.
Alternatively, the focusing may be automatically performed with use
of a programmable computer. Movement of one or more components of
the detection system is illustratively shown in FIG. 2 by arrows
123.
[0077] In this particular embodiment of FIG. 2, the DNA chip 14,
the electronic light detector array 4, and the optical filter 17
are in direct contact with one another. In other words, one side
124 of the DNA chip 14 is in direct contact with, i.e., touching,
one side of the optical filter 17, and further, the other opposing
side of the optical filter 17 is in direct contact with one side of
the detector 4 that includes detector pixels 5 for sensing light
that impinges thereon.
[0078] However, one skilled in the art will recognize that although
direct contact is preferred in some embodiments, in various other
embodiments described herein, the components need not be in direct
contact with one another. For example, the present invention may
function suitably with the components in close proximity to one
another at a distance that is suitable to accomplish mapping of
pertinent information from the biological sample to a suitable
number of detector pixels, e.g., a DNA spot to a few detector
pixels. Generally, a distance of less than 100 mm is a distance
less than, and which may provide beneficial advantages over, other
microscopic detection systems that employ objective lens type
optical systems.
[0079] Preferably, the sampling distance (or the traveling distance
for light emanating from one or more portions of the sample to
reach the detector pixels 5, i.e., the light path) for use in
detection of spots of polynucleic acid or other biological material
is of a shorter distance, e.g., a shorter light path, than used in
such microscopic detection systems employing objective lens type
systems as such shorter light paths provide for improved capture of
light. Preferably, the light path in one or more embodiments herein
is less than one centimeter; more preferably, the light path is
less than four millimeters; even more preferably, the light path is
less than one millimeter; more preferably, the light path is less
than 200 microns; yet more preferably, the light path is less than
75 microns; yet even more preferably, the light path is less than
35 microns; and most preferably, the light path is less than 15
microns. Yet further preferably, the light from the sample surface
travels a substantially linear light path to the detector pixels
5.
[0080] In at least one embodiment, every point of the light path
between where light leaves the biological sample and the detector
pixels 5 has an index of refraction that is greater than 1.0.
Further, in at least one embodiment, the light path is formed of
solid materials. e.g., light travels through components that are in
direct contact.
[0081] A light-tight enclosure 20 is provided to house components
of the image detection apparatus 101 as shown in FIG. 2. The light
105 is directed through an aperture 16 and impinges on the DNA chip
14. In this particular embodiment, light 105 causes the emission of
light from one more regions or portions of the DNA chip 14 that is
excited by the ultraviolet or blue light 105. This emitted light
from the excited regions of the DNA chip 14 passes through the chip
substrate and an optical filter 17. The excitation light, e.g., the
ultraviolet and/or blue light, is removed by the optical filter 17.
The emitted light is then allowed to impinge on the detector pixels
5 of the electronic light detector array 4, e.g., a CMOS detector.
For example, a CMOS detector 4 may contain circuitry that converts
sensed analog light impulses to digital form, which can then be
transmitted to computer 8, and ultimately after processing be
displayed as reconstructed image 18 on a monitor 11.
[0082] An optical filter, as used herein, refers to a light filter
that blocks or redirects the passage of some wavelengths of light
and allows or redirects the passage of other wavelengths of light
depending upon the application in which it is used, e.g., selective
passage or redirection. Any suitable optical filter capable of
performing such filter functions for a particular application may
be used according to the present invention. Such optical filters
include, for example, edge filters, narrow band filters, dichroic
mirrors, and optical filters such as those used in the
visualization arts, including optical, ultraviolet, confocal, and
two- or multi-photon microscopy.
[0083] The light sources as used herein may include, for example,
those commonly used in the visualization arts, including optical,
ultraviolet, confocal, and two-photon or multi-photon microscopy.
Further, for example, such light sources may include light lamps,
LED cluster arrays, tungsten filaments, and light lasers, such as
visible-light lamps, ultraviolet lamps, mercury lamps, and lasers,
including argon lasers, helium-cadmium lasers, semiconductor
lasers, LED lasers, etc.
[0084] With reference to the embodiment of the present invention
shown in FIG. 2, an image detection apparatus 101 and method for
detecting a pattern of, for example, polynucleic acid hybridization
to a biological sample surface 14, e.g., a surface of a DNA chip
14, is further described. For example, the image detection
apparatus 101 may include a positioning device, e.g., the clamping
structure 19, for receiving a nucleic acid chip 14 and maintaining
the chip 14 in a sampling position. The nucleic acid chip 14 is
generally an object with a flat sample surface 114 and an opposed
surface 124 that is joined to the sample surface 114 by a
thickness. The sample surface 114 has sequences of nucleic acids
immobilized thereto, with each sequence being immobilized to a
particular chip address. Further, the electronic light detector
array 4 includes the detector pixels 5 on side 119 of the
electronic light detector 4. The detector pixels 5 include sensors
located at particular detector pixel addresses. The sampling
position places the sample surface 114 of the chip 14 at a defined
position relative to the electronic light detector array 4 such
that light leaving a chip address on the chip 14 is substantially
directed through the light path that includes the biological
material holding structure, e.g., DNA chip substrate, onto at least
one detector pixel 5 with an address that is correlated to the chip
address. In such a manner, the nucleic acid spots on the chip 14
are mapped to the detector pixels 5.
[0085] In one embodiment, a detection system according to the
present invention, such as, for example, the system shown in FIG.
2, may be configured to excite, detect, filter, and process
fluorescence from conventional fluorophores, for example,
fluorophores described in catalogues published by Life
Technologies, Inc. (Rockville, Md.), Sigma-Aldrich, Inc. (SIGMA,
ALDRICH, and FLUKA brand names; St. Louis, Mo.), Pierce Chemicals
(Rockford, Ill.), and other suppliers known to those skilled in the
art. Similarly, other DNA visualization techniques are currently
known and used, and many examples of these technologies are set
forth in these same sources. For instance, colorimetric systems
that create a color in the visible light wavelength, for instance
those based on a stain or on enzyme activity, may be adapted to
visualize DNA. Amplification systems that may be used in
combination with a colorimetric or fluorescent system may also be
used; for example, avidin-biotin or antibody-based techniques. For
example, the target DNA labeled with biotin may be placed on the
DNA chip. After a washing protocol is performed, the sample may be
exposed to labeled avidin, which makes a strong bond to the biotin.
The label on the avidin may be a fluorophore (or an enzyme such as
horseradish peroxidase (HRP) that is suitable for colorimetric
assay). Additionally, DNA may be marked or labeled using
chemi-luminescence or chemi-fluorescence and subsequently
detected.
[0086] DNA may be attached to biological material holding
structures such as substrates, e.g., forming DNA chips, that pass
light (e.g., light transparent DNA chips) in a variety of manners
known to those skilled in the art. For example, glass or quartz may
be treated with silanes to create carboxyl or amine groups that may
be used in further chemical reactions for immobilizing DNA.
Further, a light transmissive plastic such as polystyrene may be
used for the DNA chip substrate. Various techniques known to those
skilled in the art are included in the patents incorporated by
reference, above, as well as in the following references, which are
incorporated herein by reference: Laursen et al., "Solid Phase
Methods in Protein Sequence Analysis Methods of Biochemical
Analysis," vol. 26 John Wiley & Sons, Inc. 1980, pp. 202-215;
"Immobilization of oligonucleotides onto a glass support via
disulfide bonds: A method for preparation of DNA microarrays,"
Rogers Y H, Jiang-Baucom P, Huang Z J, Bogdanov V, Anderson S,
Boyce-Jacino M T. Anal Biochem 1999 Jan. 1, 266(1):23-30; "Covalent
attachment of DNA oligonucleotides to glass," Cohen G, Deutsch J,
Fineberg, J, Levine A, Nucleic Acids Res 1997 Feb. 15, 25(4):911-2;
"Hybridization of DNA targets to glass-tethered oligonucleotide
probes," Beattie W G, Meng L, Turner S L, Varma R S, Dao D D,
Beattie K L, Mol Biotechnol 1995 Dec., 4(3):213-25; "Preparation of
glass plates with cerium oxide for DNA sequencing," Millard D, de
Couet H G, Biotechniques 1995 Oct., 19(4):576; "Biologically
Functional Materials," Allan S. Hoffman, in Biomaterials Science,
B. D. Ratner, A. S. Hoffman, F. J. Schoen, and J. E. Lemons, Eds.,
pp. 124-130.
[0087] Further, various embodiments of the present invention as
described herein (e.g., bar code reader type embodiments) may
provide for imaging of DNA chips that are not light transparent.
e.g., substrates that do not pass light. For example, such
substrates may include various materials generally used to provide
DNA chips. As such, depending upon the detection system
configuration, a DNA chip may or may not need to be light
transparent.
[0088] The invention may be used with DNA or with other
combinations of hybridizable molecules, for instance RNA-DNA or
DNA-protein interactions. DNA-DNA hybridization has been used as an
example but the invention may be used with all polynucleic acid
hybridization techniques, including RNA-RNA hybridization. As
described previously herein, polynucleic acid, as used herein,
means DNA, RNA, two or more oligonucleotides or oligonucleosides,
and all long or short sequences of nucleic acids. A "DNA chip" or
"polynucleic acid chip" as used herein is one type of biological
sample that is generally classified as a type of micro-array. A DNA
chip generally refers not only to DNA sequences immobilized on
small solid substrates, but also refers to RNA, etc., and generally
to any device, substrate, or other object with biomolecules
immobilized thereto. However, a biological sample, as used herein,
is clearly not limited to a DNA chip and refers to other types of
biological samples such as 1-D and 2-D gels, etc.
[0089] FIGS. 3A-3B illustrate two alternative optical
configurations for the image detection apparatus 101 for use in
direct mapping according to the present invention. In FIG. 3A, the
sampling surface 114 of the DNA chip 14 is in contact with a first
side 115 of the optical filter 17. The second side 117 of the
optical filter 17, i.e., the side opposite the first side 115, is
in direct contact with a surface 119 of the detector 4 upon which
the detector pixels 5 are located. As such, for example, excitation
light transmitted through the substrate of the chip 14 excites the
biological material on the sample surface 114 and any fluorescence
is transmitted through the filter 17 to the detector pixels 5 of
the detector 4, e.g., CMOS detector array.
[0090] One skilled in the art will recognize that the opposing
surface 124, i.e., opposite the sampling surface 114, of the DNA
chip 14 may be in contact with a first side 115 of the optical
filter 17. In the imaging process, light emanating from the sample
surface 114 of the chip 14 is then transmitted through the chip
substrate to the detector pixels 5 of the detector 4, e.g., CMOS
detector array.
[0091] In FIG. 3B, the DNA chip 14 is in sequence with a mapping
lens 21. The sampling surface 114 of the DNA chip 14 is in direct
contact with a first side 129 of the mapping lens 21. The second
side 131 of the mapping lens 21, i.e., the side opposite the first
side 129, is in direct contact with a first side 115 of the optical
filter 17. The second side 117 of the optical filter 17, i.e. the
side opposite the first side 115, is in direct contact with a
surface 119 of the detector 4 upon which the detector pixels 5 are
located. In the imaging process, light from the chip 14 is focused
by the mapping lens 21 through the filter 17 to the detector pixels
5 of the detector 4, e.g., CMOS detector array. Preferably, the
mapping lens 21 has a focal length suitable for focusing the light
emitted by the chip 14 onto the detector pixels 5 of the detector
4. Yet further, the mappings lens may be a lens configured for
collimating light impinging thereon. As in the embodiment of FIG.
3A, the opposing surface 124 of the DNA chip 14 may be in direct
contact with the first side 129 of the mapping lens 21.
[0092] The theoretical resolving power of the image detection
apparatus and methods described above will be directly related, at
least in part, to the spacing between the DNA chip light emitting
regions, e.g., the sampling surface 114 on which the nucleic acid
spots are positioned, and the surface 119 upon which the imaging
detector pixels 5 are located, i.e., the length of the light path.
The actual resolving power will also be a function of the emission
from the DNA spots and the sophistication of the software used to
extract and reconstruct the light therefrom, e.g., the DNA
fluorescence.
[0093] Further, the theoretical resolving power of the
configuration including a simple mapping lens 21 or lens system
will be limited by the optical quality of the mapping lens 21 and
by light diffraction. However, it is not the goal of this system to
have high cost resolution imaging optics as part of the present
detection apparatus since low cost optics with suitable software
will readily map arrays of DNA pixels.
[0094] The resolving power of direct mapping can be computed as the
sum of: the larger of the detector pixel diameter (e.g., roughly 10
.mu.m) or spot diameter; chip 14 thickness (e.g., 10 .mu.m); and
filter thickness (10 .mu.m). Thus, the image from a 10 .mu.m DNA
spot (assuming the chip thickness and filter thickness are both
about 10 .mu.m) would map onto a 30 .mu.m.times.30 .mu.m area of
the detector containing 9 detector pixels, while the image from a
50 .mu.m DNA spot (assuming the chip thickness and filter thickness
are both about 10 .mu.m) would map onto a 70 .mu.m.times.70 .mu.m
area containing 49 detector pixels. For example, a CMOS device such
as the HDCS-1100 (Hewlett-Packard Components Group; Corvallis,
Oreg.) which has a 352.times.288 detector pixel array, can resolve
approximately 1,000 spots that are 10 .mu.m in diameter, and
approximately 2,000 spots that are 50 .mu.m in diameter.
[0095] The detector pixels of suitable electronic light detector
arrays may also integrate light emission with time, in much the
same way that longer photographic exposure is used to develop faint
images. This time integration will permit the detection of any
light impulse that can be detected with a computer-assisted
confocal microscope so long as the fluorescence signal exceeds
detector dark current and background light.
[0096] Further, the optical system of the invention (for example a
single mapping lens) can magnify or reduce the image. A mapping
lens would permit the emissions from the DNA chip to be optimally
projected onto the detector pixels of a CMOS device. For instance,
a reducing mapping lens may be capable of mapping the emission from
a 50 .mu.m spot onto an individual detector pixel.
[0097] FIG. 4 is a block diagram of a system substantially similar
to that of FIG. 2, wherein light from a biological sample, such as
a DNA chip 14 having biological material 13 thereon, is passed
through an optical filter 17 and provided to detector pixels 5 of a
detector 4, e.g., a CMOS or CCD detector, where such light is
sensed. Signals representative of the sensed light may be
digitized, relayed to computer 8, and subsequently processed and
displayed as an image 18 on the computer's monitor 11. The image
detection apparatus 101 of FIG. 4 may be modified with various
light sources in various configurations thereof.
[0098] For example, the system shown in FIG. 4 is compatible with
laser-based visualization techniques as shown in FIG. 5. In other
words the image detection apparatus 101 of FIG. 4 may be modified
to be in the configuration shown in FIG. 5. For instance, a laser
40 may be used to generate laser light 41 that may be reflected off
of mirror 35 and thereby directed onto labeled DNA 30 hybridized
and immobilized on DNA chip 14. In view of the incorporation of a
fluorescent label, the hybridized DNA 30 fluoresces and emits
fluorescent light upon excitation by the laser light 41. The filter
17 selectively passes the fluorescent light but not the laser light
41. The fluorescent light is directly mapped onto the detector
pixels 5 of detector 4, e.g., a CCD detector array. The laser 40
may be rastered across the biological sample, e.g., the DNA chip
14, so that only select portions of the sample are illuminated at
one time. The laser 40 may be, for example, laser diodes such as
green (532 nm), red (635 nm), or far red (670 nm) diodes having a
power in the range of 4 mW to 10 mW.
[0099] The system of FIG. 4 may also use a lamp-type light source
15 as shown in the dichroic mirror arrangement of FIG. 6. As shown
therein, the lamp-type source 15 emits light 43 that is reflected
off a dichroic mirror 36 onto immobilized, labeled, and hybridized
DNA 30. If the label on the hybridized DNA 30 is a fluorescent
label, then the fluorescence emitted in response to excitation by
light 43 may pass through dichroic mirror 36 and be mapped directly
onto a detector 4, e.g., CCD detector array. An image
representative thereof may be displayed on a computer monitor or
stored in a computer memory using the techniques already
described.
[0100] As shown in FIG. 6, direct mapping may still be accomplished
even though the emitted light from the DNA spots is not provided
through a light transparent DNA chip 14. In this embodiment, the
biological material 30 is provided on a sample surface 14 that
faces the dichroic mirror 36. The light from the sample surface 114
including the biological material 30 is filtered by the mirror 36
and impinges on the detector pixels 5 that are also facing the
dichroic mirror 36. In other words, in this configuration, the
detector 4 and biological sample, e.g., DNA chip 14, are separated
by a dichroic mirror 36 that performs the filtering function.
Further, the DNA chip 14 need not be transparent as the sample
surface 114 is facing the detector pixels 5. In other words, the
light path from the sample surface 114 to the detector pixels 5 is
not through the substrate or biological material holding structure
of the biological sample associated with the biological
material.
[0101] Yet further, in some embodiments described herein, an
excitation filter between a light source and the biological sample
may be needed to filter out certain light from the light source
that may interfere with the detection of certain light
wavelength.
[0102] As shown in FIG. 7, a mapping lens 3 may be used to enhance
the direct mapping of the system described above with reference to
FIG. 6 incorporating a dichroic mirror 36. The mapping lens 3 will
focus light that passes through dichroic mirror 36 such that DNA
chip pixels of the DNA chip 14 are mapped onto one or more of the
detector pixels 5 of detector 4, e.g., a CCD detector 4.
[0103] As an alternative arrangement to certain embodiments
described herein, creation of a negative image may be performed.
Numerous techniques and combinations of components for making
negative images will be immediately apparent to those skilled in
the art upon reading this disclosure. A few examples are provided
herein but are in no way intended to limit the present invention. A
negative image could be made by causing DNA to appear as a dark
spot on a bright field. For instance, a bright fluorescent field,
created by making the substrate of the DNA chip 14 with
autofluorescent components, could be used with a label on
hybridized DNA 30 that quenches or blocks light. The hybridized DNA
would then appear as dark spots on a computer generated image.
Compounds that quench fluorescence are known to those skilled in
the art.
[0104] Alternatively, hybridized DNA could be labeled after it is
immobilized to the DNA chip 14. For instance, a stain that blocks
transmission of visible light may be used. Further, the DNA could
already incorporate a label that could be calorimetrically
developed after the DNA is immobilized, e.g., the hybridized DNA
might have an enzyme that would cause a colored precipitate to form
when the chip was exposed to a suitable substrate, such as, for
example, a horse radish peroxidase (HRP) system could be used. Yet
further, the immobilized DNA might have a fluorescent molecule that
was quenched by elements on the hybridizing DNA.
[0105] The previous embodiments described may be configured without
an optical filter 17 as shown in FIGS. 8A-8C. For example, a light
transmitting DNA chip 14 with hybridized DNA 32 on a biological
material holding structure 131 as shown in FIG. 8A may be treated
so that the hybridized DNA appears as dark spots that fully or
partially block light. The DNA chip may then be positioned as shown
in FIGS. 8B or 8C. As shown in FIG. 8B, the sample surface 114 is
positioned opposite the detector pixels 5 of detector 4. In other
words, the side 124 of DNA chip 14 opposing the sample surface 114
faces the detector pixels 5.
[0106] As shown in FIG. 8C, the sample surface 114 faces the
detector pixels 5 of detector 4. In other words, the sample surface
114 of the DNA chip 14 is on the side opposite the light source 43.
A cover 52 may be interposed between the sample surface 114 having
the DNA spots 32 thereon and the detector pixels 5 so that detector
4 is not degraded by the DNA spots 32. The cover 52 may be a mere
protective film such as a coating, or a coverslip, a plastic wrap
such as polyethylene film, or any other material that transmits the
wavelength of the light 43.
[0107] In the configurations shown in FIGS. 8B and 8C, light 43
(such as shown in the embodiment of FIG. 7) from a light source
passes though DNA chip 14 but is blocked by light-blocking
hybridized DNA 32. The resultant map that is formed on detector 4,
e.g., a CCD detector array, shows the addresses that have
hybridized DNA. Many fluorescent and non-fluorescent techniques for
labeling DNA before or after its hybridization to DNA or before or
after its immobilization to the DNA chip 14 are known to those
skilled in these arts. Light 43 may be any wavelength specified
herein as light and DNA 32 may be any means for blocking that
transmission that is known to those skilled in the art.
[0108] It is noted that, in FIGS. 8B and 8C, no optical filter is
used in the light path between the sample surface of the DNA chip
14 and the electronic light detector 4. All wavelengths of the
source light 43 are allowed to reach the detector pixels 5 of the
detector 4. However, a neutral density filter may be used in the
light path between the sample surface and the detector 4. The
neutral density filter may be used to block some of the source
light 43 without filtering out any wavelengths of light.
[0109] The filters 17, lenses 3, and biological samples, e.g., DNA
chips 14, shown in many of the embodiments described above may be
used in various combinations as exemplified in FIGS. 9A and 9B. For
example, a lens and filter may be combined into lens-filter 50 that
is interposed between the DNA chip 14 and detector 4 as shown in
FIG. 9A. Further, for example, the DNA chip 14 may be made as part
of an integral single DNA chip-filter 51 that provides a solid
substrate for DNA immobilization and acts to filter the light 43
from the light source or from the immobilized DNA 30 as shown in
FIG. 9B. Materials or coatings used for filters are well-known to
those skilled in the optical arts. The optical coating is generally
formed on the surface of the chip 14 opposing the sample surface.
In one embodiment, the optical coating allows passage of light
wavelengths of fluorescence but substantially blocks other light
wavelengths in the range of 300 nanometers to 600 nanometers.
[0110] Further, the DNA chip 51 may include an optical lens along
with or in addition to the filter. For example, the surface of the
DNA chip opposing the sample surface may be a curved surface that
functions as a mapping lens. Preferably, the optical lens has a
minimum focal length of 10 microns and more preferably 5 microns.
Further, preferably, the optical lens has a maximum focal length of
750 microns; more preferably, 400 microns; yet more preferably, 250
microns; and most preferably, 40 microns. Such focal lengths are
applicable to the other embodiments using mapping lenses as
described above.
[0111] FIG. 10 shows another alternate embodiment of an image
detection apparatus 201 according to the present invention. The
image detection apparatus 201 may be referred to as a lens-free
transmission light microscope as no lenses are necessary to perform
the desired imaging. For example, the microscope or image detection
system 200 may be used to resolve images with features as small as
10 .mu.m in diameter. The image detection apparatus 201 is a
transmissive imaging configuration as the configuration provides
for detection of light from a biological sample 208 which has
biological material 213 on a sample surface 209 thereof, and which
requires the use of transmitted light through all, or at least a
major portion of, the biological material holding structure 211,
e.g., DNA chip substrate gels that may be associated with a
substrate or imaged alone, etc.
[0112] In other words, at least in the embodiment shown in FIG. 10,
the transmitted light from a fiber optic bundle 220 illuminates or
excites the biological sample 208, e.g. a light absorbing sample or
a fluorescent producing sample. Light from the biological sample
208 then travels through the light path that includes the
biological material holding structure 211 of the biological sample
208 to impinge on the electronic light detector 210. In other
words, for the electronic light detector 210 to detect light from
the biological sample 209, light is passed through or transmitted
through the biological holding structure of the biological sample
208. In this embodiment, the biological holding structure of the
biological sample 208 must be light transmissive structure, e.g.,
glass, clear materials, or other materials that permit transmission
of suitable or desirable wavelengths of light.
[0113] The detection system 200 of FIG. 10 generally includes a
light source 202, polarizing filters 215-216, a fiber optic bundle
apparatus 220, an electronic light detector and associated
circuitry 210 (e.g., CCD array or CMOS array), a computer 8 having
memory 108 for use in storing any necessary software for carrying
out the present invention and/or for analyzing any image data from
the image detection apparatus 201, and a monitor 11 or some other
output device for interfacing with a user. In general, parallel
light rays are produced that are passed perpendicular to sample
surface 209 of the biological sample 208, e.g., a microscope slide
having, for example, light absorbing biological material or
fluorescence producing biological material thereon. A transmission
pattern of light through the biological material holding structure
211, e.g., the light transparent slide, is acquired by the
electronic light detector 210 and captured by suitable image
acquisition software associated with the detector 210 to produce
image data. The image data may be provided for display on monitor
11 using computer 8.
[0114] In further detail with reference to FIG. 10, the light
source 202 provides light that impinges on the first polarizing
filter 215. Optionally, the light from the light source 202 may
impinge on a receiving end 221 of the fiber optic bundle apparatus
220 as the first polarizing filter 215 may optionally be positioned
between the fiber optic array 217 and the biological sample 208
instead of between the light source 202 and the fiber optic bundle
apparatus 220. A second polarizing filter 216 that is orthogonal or
90 degrees rotated from the first polarizing filter 215 is
positioned between the biological sample 208 and the electronic
light detector 210. The polarizing filters are linear polarizers
that prevent the electronic light detector 210 from oversaturation.
Such oversaturation may reduce the dynamic range of the detector
210. Further, the polarizing filters 215-216 provide for the
filtering of zero order diffraction in the system. The light source
202 may be any suitable light source such as a clustered white LED
light source, a tungsten filament, or any other light source
previously described herein.
[0115] The polarizing filter 215, if positioned between the light
source 202 and the fiber optic bundle apparatus 220, provide the
polarized light onto the receiving end 221 of the fiber optic
bundle apparatus 220. The fiber optic bundle apparatus 220
generally includes the receiving end 221 of a bundle portion 204.
The bundle portion 204 is then fanned out in a fanout bundle
portion 222 and terminated at a fiber optic array portion 217,
e.g., a one-dimensional (in-line or linear) array. For example, the
fiber optic array portion 217 may include termination fiber ends
207 of individual fibers 205 positioned separately in openings of a
fiber optic array holder 227 (shown in further detail in FIG. 11).
The fiber optic array portion 217 provides for the illumination of
the biological sample 208.
[0116] Light transmitted through the biological sample 208, e.g.,
the biological sample holding structure 211 associated with
biological material 213 thereof, impinges on detector pixels 219 of
the electronic light detector 210 and an image is detected
representative of the biological material 213 of the biological
sample 208. For example, if the biological sample 208 is a
micro-array having fluorescent tagged nucleic acids thereon, then
fluorescence would be transmitted through the light transparent
micro-array substrate, onto the electronic light detector 210 (in
this case, an emission filter may be required to prevent
transmission of the excitation light from the fiber bundle from
reaching the electronic light detector). Further, for example, if
the biological sample 208 is a silver-stained DNA micro-array or
chip, then such a light absorbing biological sample will absorb
light and a transmission pattern representative of the light
absorbed at particular locations will be transmitted through the
substrate or holding structure of the DNA chip. The transmitted
pattern will then be acquired by the electronic light detector
210.
[0117] The biological sample 208, the polarizing filter 216 and the
electronic light detector 210 may be positioned in any suitable
manner as previously described herein such as shown in FIGS. 2-5
and 8-9. For example, as shown in the embodiment of FIG. 11, the
biological sample 208, polarizing filter 216, and the electronic
light detector 210 are in direct contact with one another, with the
electronic light detector 210 separated from the biological sample
only by the thickness of the polarizing filter 216, which may, for
example, have a thickness of about 1/2 millimeter. Preferably, the
biological sample 208 and the detector pixels 219 of the electronic
light detector 210 are as near one another as possible, at least in
this particular embodiment. However, in no manner is the present
invention limited to configurations that have one or more of the
above elements, e.g., biological sample 208, the polarizing filter
216 and the electronic light detector 210, in direct contact. For
example, the present invention may be employed with such elements
in close proximity to one another.
[0118] Generally, in operation, the fiber optic array portion 217,
e.g., a linear array of optical fibers, is scanned across the
biological sample 208 using known scanning mechanics 223 generally
represented in FIG. 10. For example, such scanning mechanics may
include mounting structures, stepper motors, piezo-electric
actuating elements, etc. Such movement may be controlled by a
computer 8 under command of suitable software in memory 108. The
present invention is not limited to any particular movement
mechanics 223 as any scanning mechanics, at least in this
particular embodiment, that can provide for linear movement will be
suitable.
[0119] In other words, the linear array 217 of fibers is scanned
across a stationary biological sample 208 such that the transmitted
light from the biological sample 208 resulting from the
illumination thereof is provided to one or more detector pixels of
the electronic light detector 210. As such, a corresponding array
of detector pixels, e.g., one or more detector pixels per fiber,
detect light from the biological sample 208. A suitable image
acquisition software program, such as a stitching program, may then
be used to provide for combination of the scanned and detected
captured image data to present a composite image data file that may
be displayed or otherwise provided as output to the user. For
example, image data from multiple arrays of detector pixels
representative of portions of the biological sample 208 acquired
during a scan of the biological sample 208 by the fiber array 217
may be combined to form a complete image of the biological sample
208.
[0120] Alternatively, the biological sample 208 may be moved by
movement mechanics 223 such that image data representative thereof
can be captured. In other words, with the fiber optic array 217 and
the electronic light detector 210 held stationary the biological
sample 208 is moved such that the light from the individual fibers
205 of the array 217 impinge sequentially upon different linear
portions of the biological sample 208 as it is moved. At each of
the linear portions, light is detected, e.g., at an array of
detector pixels or on a single linear array of pixels, from the
biological sample 208. Upon capture of all desired linear portions
thereof, suitable image acquisition software is used to combine the
detected linear portions into a composite image data file
representative of the biological sample 208, or at least a portion
thereof.
[0121] Although use of a linear electronic light detector, e.g., a
linear CCD, is possible, preferably, the light from the biological
sample impinged upon by light from a single fiber is mapped to more
than one detector pixel so as to provide more data for combining
detected linear portions of the sample. In other words, with more
pixel data available for each corresponding illumination fiber end
207, a sharper image can be created.
[0122] FIGS. 11A-11C provide an illustrative exemplary and more
detailed configuration of the image detection apparatus 201 of the
detection system 200 generally shown in FIG. 10. The detection
apparatus 201 generally includes a light source 202, polarizing
filters 215-216, a fiber optic bundle apparatus 220 (shown in two
sections in FIG. 11A connected by line 260), an electronic light
detector 210 and associated image acquisition circuitry 211 (e.g.,
CCD array or CMOS array and associated hardware and software). As
shown in FIG. 11A, the light source 202 includes a clustered white
LED array 240 that provides light that impinges on the first
polarizing filter 215. The first polarizing filter 215 is
positioned adjacent to a collimator 242. As such, light polarized
by the filter 215 is provided through the collimator 242. For
example, the collimator may be a long tube or any other type of
collimator used by those in the art, such as an optical pipe
capable of collimating the light.
[0123] The collimator 242 is attached for provision of light
therefrom to the receiving end 221 of a fiber optic bundle portion
204 of the fiber optic bundle apparatus 220 using a coupling 248,
such as a grommet. The bundle portion 204 is then fanned out into a
fanout bundle portion 222 or individual fibers 205 with each fiber
terminated at a fiber optic array portion 217, e.g., a
one-dimensional (in-line or linear) array. The fiber optic array
portion 217 includes termination fiber ends 207 of individual
fibers 205 positioned separately in openings of a fiber optic array
holder 227 as shown in FIG. 11B. The fiber optic array portion 217
provides for the illumination of a linear portion of the biological
sample 208.
[0124] As described above with reference to FIG. 10, the biological
sample 208, the second polarizing filter 216, and the electronic
light detector 210 can be provided in numerous configurations. As
shown in FIG. 11A, the biological sample 208, polarizing filter
216, and the electronic light detector 210 are in direct contact
with one another, with the electronic light detector 210 separated
from the biological sample 208 only by the thickness of the
polarizing filter 216. The second polarizing filter 216 is
orthogonal or 90 degrees rotated from the first polarizing filter
215 such that suitable filtering of at least zero order diffraction
in the system is provided.
[0125] Light transmitted through the biological sample 208, e.g.,
the biological sample holding structure associated with biological
material thereof impinges on detector pixels of the electronic
light detector 210 and an image is detected representative of the
biological material 213 of the biological sample 208. The image is
captured using suitable image acquisition circuitry and software
211 such as described above, e.g., image combining software. For
example, such software and/or hardware may include software that
can patch together the portions using overlapping information to
provide additional resolution, such portions may be pieced together
through storage individually in memory, etc.
[0126] As shown in the plan view of the face 261 of the fiber optic
array portion 217 in FIG. 11B, individual fibers 205 terminate at
fiber ends 207. Each fiber 205 is terminated in a corresponding
opening of a fiber optic array holder 227. The fiber optic array
holder 227 is associated with brackets 219 for connection to a
stepper motor for movement to be controlled by computer 8 under
command of suitable software.
[0127] FIG. 11C is a side view of the fiber optic array portion 217
shown in FIG. 11B. As shown therein, the individual fibers 205
terminate at ends 207 after insertion through openings in the
holding structure 227. As previously described above with reference
to FIG. 10, the fiber optic array portion 217 is scanned across the
biological sample 208 and image data representative thereof is
captured. For example, as the fiber optic array portion 217 is
scanned across linear portions of the biological sample 208, the
electronic light detector captures light from such linear portions.
Thereafter, such detected linear portions may then be combined to
form a composite image of the biological sample 208.
[0128] As previously described herein, reflective imaging
configurations refer to configurations that provide for detection
of light from a biological sample, e.g., a sample surface at which
biological material is associated, which does not require the use
of transmitted light through the biological holding structure of
the biological sample, or a major portion thereof, e.g., DNA chip
substrate, micro-titer plates, gels that may be associated with a
substrate or imaged alone, etc. Preferably, in a reflective imaging
configuration, light (whether excitation, fluorescence, or
reflected light from a biological sample) does not pass through the
biological holding structure of the biological sample, or at least
does not pass through a major portion thereof. In such cases, the
biological holding structure need not be light transparent
structure, but rather can be opaque materials, e.g.,
nitrocellulose, charged nylon, silicon as a substrate for
micro-array formation, etc., which have more favorable properties
than light transparent structure (e.g., glass).
[0129] Such a reflective imaging configuration is shown by the
electronic light detector array detection system 300 generally
shown in FIG. 12. The electronic light detector array detection
system 300 generally includes an image detection apparatus 302 for
capturing one or more frames of an image, e.g., image data,
preferably in digital form, representative of a biological sample
304 held in a stationary location (e.g., sampling position) by
positioning structure 321. The image data is then provided to a
computer 310 for reconstruction, storage in memory and/or analysis
thereof. For example, the image data may be mapped to the computer
memory 108 and processed to provide data representative of a
reconstructed image for display on a monitor 11, e.g., a computer
display or any other display apparatus that may display image data
representative of the reconstructed image 12. Such reconstruction
may use one or more frames of image data.
[0130] The positioning structure 321 may be any structure or
mechanisms available for maintaining the biological sample 304 in a
fixed position. For example, the positioning structure may include
clamps, clips, wells, adhesives, etc. Further, such positioning
structure may include movement mechanisms for moving the biological
sample 304 into multiple sampling positions and locking the sample
into the fixed sample position. For example, such movement may be
used to focus an image as previously described herein.
[0131] The image detection apparatus 302 generally comprises a
light source 330 located for providing light 306 (e.g., excitation
light or illumination light) onto the biological sample 304, or at
least a portion thereof. Further, the image detection apparatus 302
comprises an electronic light detector 324 and a lens 320 for
focusing light 308 (e.g., fluorescence or reflected light) from the
biological sample 304 onto detector pixels 327 of an electronic
light detector 326. The electronic light detector 324 is operable
under control of control circuitry 326, e.g., a frame grabber. For
example, the control circuitry 326 receives the sensed signals from
the electronic light detector 324 and captures one or more frames
of images to be used for later processing and/or display. Further,
optionally, in the situation where the image detection apparatus
302 is used for detecting fluorescence as further described below,
the image detection apparatus 302 also includes an interchangeable
emission filter 350.
[0132] The image data may then be provided by the image detection
apparatus 302 to a port of the computer 310. The image data may
then be operated on by graphics manipulation software to, for
example, reconstruct the image data and display a visual image on
the monitor 312. Various types of software may be used. For
example, QuickView (a Windows.RTM. application program) may be used
to capture, save and categorize images and ImagePro Plus available
from Media Cybernetics may be used for manipulation of graphics;
etc.
[0133] Generally, the image detection apparatus 302 may be provided
using a modified bar code reader such as a bar code reader
available under the trade designation of WelchAllyn IMAGETEAM
4710HD/HD10 handheld or fixed mount 2D image reader. For example,
the light source of the available 2D image reader may be modified
to provide a light source as further described below and an
emission filter may be added for use in fluorescent marker
applications.
[0134] The image detection apparatus 302 may be used to image
fluorescence, e.g., detect fluorescent probes or markers bound to
specific locations on DNA chips such as in genomics research or
fluorescent labeled proteins separated by two-dimensional gel
electrophoresis such as in proteomics research. For example,
biological samples 304 of considerable size, such as in the case of
2-D gels which can be relatively large (e.g., 25.4 cm.times.25.4
cm) can be imaged successfully. For example, preferably, with use
of reducing lenses, biological samples 304 as large as 50
cm.times.50 cm may be imaged.
[0135] With respect to imaging fluorescence and with reference to
FIG. 12, the biological sample 304 provides biological material
including fluorescent markers associated with a biological material
holding structure, e.g., a gel or a micro-array such as a DNA chip.
For example, such biological material including the markers may be
at particular addresses of the micro-array that correspond to
addresses of one or more detector pixels. Excitation light 306 is
directed onto the sample surface 304 to excite the fluorescent
markers or cause excitation events that produce fluorescent light
photons of characteristic wavelength. Such fluorescent light 308 is
passed through the lens 320, focused and projected as an image
representative of the fluorescence from the excited sample onto the
detector pixels 326 of the electronic light detector 324. The
excitation light reflected by the sample surface 311 is prevented
from reaching or is blocked from the electronic light detector 324
and lens 320 by the emissions filter 350. The electronic light
detector 324, e.g., a two-dimensional array detector, under control
of circuitry 326, grabs a frame of the fluorescence image and
provides the image data for reconstruction alone, or more
preferably in combination with one or more other frames of image
data.
[0136] With respect to imaging reflected light, i.e.,
representative of the absorption characteristics of the biological
sample 304, and with reference to FIG. 12, the biological sample
304 provides biological material that for example, may be stained
or otherwise detectable such as with the use of color, density,
etc. The biological material is associated with a biological
material holding structure, e.g., a gel or a micro-array such as a
DNA chip. Illumination light 306 is directed onto the sample
surface 311 of the biological sample 304. Based on the absorption
and reflective characteristics of the biological sample 304,
reflected light is passed through lens 320 and is focused and
projected as an image representative of the biological sample 304,
e.g., stained or colored portions thereof, onto the detector pixels
326 of electronic light detector 324. The electronic light detector
324, e.g., a two-dimensional array detector, under control of
circuitry 326, grabs a frame of the reflected image and provides
the image data for reconstruction alone, or more preferably in
combination with one or more other frames of image data.
[0137] Although the image detection apparatus 302 can be used to
produce images from various biological sample configurations that
use, for example, single color fluorescence, multiple color
fluorescence, chemi-luminescence, chemi-fluorescence, colorimetric
detection, densitometry, or any other technique detectable through
imaging, the present invention is particularly beneficial for
fluorescence imaging. As such, the remainder of the description
below shall be provided with respect to such fluorescence
imaging.
[0138] For example, the image detection apparatus 302 may be used
for rapid production of single-color and multi-color fluorescence
images, e.g., images showing fluorescent positions such as regions,
spots, areas, etc., of a biological sample (e.g., fluorescent
positions on a micro-array or DNA chip) when such material is
caused to fluoresce by an excitation light or by
chemi-fluorescence. As described previously herein, a wide range of
samples, including, but not limited to gels, blots, micro-arrays,
micro-plates, etc. may be imaged to detect fluorescent positions.
The use of a modified bar code reader as presented herein provides
methods and systems that have a high sensitivity for detection of
flourescent dyes and labels, including, but clearly not limited to,
ethidium bromide, SYBR.RTM. Green, SYBR.RTM. Gold, SYPRO.RTM.,
Radiant Red, fluorescein (FITC), rhodamine, Cy2, Cy3, Texas Red,
Green Fluorescent Protein.
[0139] The modified bar code reader or image detection apparatus
302 provides multi-mode imaging with the ability to select multiple
wavelength light excitation, epi-illumination, or optionally
transmittance illumination. Multiple frames may be grabbed for a
single biological sample over time providing for improved image
resolution and uniformity. Further, as previously described herein,
the imaging area of the biological sample 304 is comparatively
large relative to other detection systems.
[0140] Two illustrative and exemplary image detection apparatus
402, 502, e.g., modified bar code readers, are shown in FIGS. 13
and 14, for use in fluorescence imaging. The image detection
apparatus 402 differs from the image detection apparatus 502 in
that the light source used for excitation is different. Each of the
configurations employs a modified WelchAllyn IMAGETEAM 4710HD 2D
image reader, although various other bar code readers may be
modified as would be readily recognized from the description
herein.
[0141] As shown in FIG. 13, the image detection apparatus 402
provides for capturing one or more frames of a fluorescence image,
e.g., image data, preferably in digital form, representative of a
biological sample 404 held in a stationary location by positioning
structure 421, e.g., any structure or mechanisms available for
maintaining the biological sample 404 in a fixed position. The
image data may be provided to computer for reconstruction, storage
in memory and/or analysis thereof such as, for example, by way of a
cable interface 465 to a serial port of a computer, or
alternatively to a universal serial bus (USB). Various other
manners of transmitting image data, such as with the use of frame
grabber techniques, may be used, e.g., wireless techniques,
parallel transmission techniques, etc. The image data may be mapped
to computer memory and processed to provide data representative of
a reconstructed image for display on a monitor, e.g., a computer
display or any other display apparatus that may display image data
representative of the reconstructed image such as previously
described herein.
[0142] The image detection apparatus 402 includes LEDs 430 for
providing excitation light 406 onto the biological sample 404, or
at least a portion thereof, e.g., the sample surface 411. For
example, any number of LEDs may be used for providing any desired
and suitable wavelength of light necessary for causing the desired
fluorescence from the biological sample 404. In one preferred
embodiment, three different wavelengths of light, e.g., 480 nm, 570
nm, and 660 nm light, are provided from 50 mW LEDs. For example,
four LEDs of each wavelength may provide enough excitation light
406 for imaging a DNA chip or a 2-D gel. The wavelengths of light
correspond to the particular fluorescent markers used. For example,
the 570 nm light provides excitation of Cy3 fluorescent labels and
the 660 nm light provides excitation of Cy5 fluorescent labels. One
skilled in the art will recognize that various other excitation
wavelengths can be incorporated into the detection apparatus
depending upon the types of flourescent markers used.
[0143] Further, the image detection apparatus 402 comprises an
electronic light detector 424 and a lens 408 for focusing
fluorescence from the biological sample 404 through the light path
onto detector pixels 426. The electronic light detector 424 may be
any two dimensional light detector, e.g., CCD detector array or a
CMOS array. Preferably, according to this particular illustrative
embodiment, the electronic light detector 424 is a black/white CCD
having the dimensions of 1/3 inch by 1/2 inch. The detector pixels
426 of the electronic light detector 424 face the sample surface
411 of the biological sample 404.
[0144] The electronic light detector 424 is operable under control
of control circuitry 426, e.g., such as the circuitry provided in a
WelchAllyn IMAGETEAM 4710HD 2D image reader. For example, the
control circuitry 426 may include a frame grabber for capturing
images sensed at a particular time by the CCD array 424, a DC
convertor for providing power to the LEDs 430 and the CCD 424, as
well as other processing circuitry capable of reading bar codes.
Such bar code processing capabilities may provide a way of
biological sample archiving as described further below.
[0145] Further, the image detection apparatus 402 also includes an
interchangeable emission filter 450. The emission filter 450 is
configured and positioned to filter or block the excitation light
or reflected excitation light 406 from the electronic light
detector 424. As such, the excitation light is prevented from
reaching the electronic light detector 424.
[0146] In operation, for example, with a biological sample 404 that
is a gel or DNA chip tagged with the fluorescent markers Cy3 and/or
Cy5, excitation light 406 is directed onto the sample surface 404
to excite the fluorescent markers such that fluorescence 408 is
produced having certain wavelengths not block from the CCD array
424 by emission filter 450. Such fluorescence 408 is passed through
lens 420 and is focused and projected as an image representative of
the fluorescence from the excited sample onto the detector pixels
427 of CCD array 424. The excitation light reflected by the sample
surface 411 is prevented from reaching or is blocked from the CCD
array 424 by the emissions filter 450. The CCD array 424 under
control of control circuitry 426 grabs a frame of the fluorescence
image and provides the image data for reconstruction alone, or more
preferably in combination with one or more other frames of image
data representative of the biological sample 404.
[0147] The distance of the image detection apparatus 402 from the
biological sample 404 is based on the focal point of the lens 420.
For example, preferably the focal point is less than 5 cm for
detecting images of a micro-array, corresponding to a light path
that is less than about 6 cm. In one particular embodiment,
distance from the lens 420 to the biological sample 404 is about 2
inches. Preferably, the closer the lens 420 can be positioned
relative to the biological sample 404, the better, as such
positioning provides for better light capture.
[0148] In more general terms, preferably, the light path between
the biological sample and the detector pixels is in the range of 4
cm to 8 cm. One skilled in the art will recognize that as the
object being imaged becomes larger, that the light path may be made
larger with concurrent modification of the lens system.
[0149] Further, as the emission filter 450 is interchangeable with
other filters for blocking different wavelengths and different
wavelengths are used for the source light, multi-fluorescent
imaging can be achieved. For example, one filter can be substituted
for another during the imaging procedure to provide images of
multiple colors that can combined into a single image for a
particular biological sample.
[0150] The image detection apparatus 502 of FIG. 14 is
substantially equivalent to that shown in FIG. 13 except that the
excitation light is provided by a laser based source as opposed to
LEDs to provide for higher resolution. As shown in FIG. 14, the
excitation light is provided by one or more lasers 570, preferably
a plurality of lasers, that provide illumination lines that are
reflected by appropriately positioned corresponding mirrors 575.
The reflected light from the mirrors 575 impinges on corresponding
dichroic prisms 580 and is passed through corresponding diffusers
585 to provide diffused excitation light 590. For example, LED
lasers having a power in the range of about 4 mW to 10 mW may be
used to produce light in the wavelength of 570 nm and 660 nm
corresponding to the Cy3 and Cy5 markers. Any number of lasers can
be used as would be known to one skilled in the art.
[0151] In accordance with one embodiment of the present invention,
a biological sample archiving method may be employed using an image
detection apparatus as shown and described with reference to FIGS.
12-14. For example, each imaged biological sample (e.g., a DNA chip
14 as shown in FIG. 8A) may include a bar code 590 (as shown in
FIG. 8A) associated therewith. As conventional bar code readers
modified herein typically are configured with the necessary
software for reading bar codes, the modified bar code reader can be
employed in a bar code reading mode to associate a particular
image, e.g., fluorescence image, with a particular imaged bar code.
Such samples may then be archived using the read and stored bar
codes associated with the corresponding fluorescence images.
[0152] Several embodiments of the invention are described herein.
These embodiments are illustrative of the present invention and are
not to be construed as embracing all of its embodiments or as
limiting on the scope thereof. It will be recognized that various
combinations of features of the present invention may be used
together to form various inventive combinations as would be
recognized from the description herein. For example, a bar code
archiving system may be used with a modified bar code reader
imaging detection apparatus, negative images may be read by the
modified bar code reader imaging detection apparatus, etc.
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