U.S. patent application number 16/192160 was filed with the patent office on 2019-10-03 for devices and methods for determining molecular structure.
This patent application is currently assigned to THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK. The applicant listed for this patent is THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK. Invention is credited to Duckhoe Kim, Ozgur Sahin.
Application Number | 20190302105 16/192160 |
Document ID | / |
Family ID | 52828766 |
Filed Date | 2019-10-03 |
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United States Patent
Application |
20190302105 |
Kind Code |
A1 |
Sahin; Ozgur ; et
al. |
October 3, 2019 |
DEVICES AND METHODS FOR DETERMINING MOLECULAR STRUCTURE
Abstract
A method of determining the structure of a molecule can include
labeling a first location on the molecule with a first DNA strand,
and measuring a force-time waveform using the twisting of a
T-shaped atomic force microscope cantilever scanning across the
molecule. The cantilever can include a DNA probe having a first
region that is complimentary to the first DNA strand.
Inventors: |
Sahin; Ozgur; (New York,
NY) ; Kim; Duckhoe; (New York, NY) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW
YORK |
New York |
NY |
US |
|
|
Assignee: |
THE TRUSTEES OF COLUMBIA UNIVERSITY
IN THE CITY OF NEW YORK
New York
NY
|
Family ID: |
52828766 |
Appl. No.: |
16/192160 |
Filed: |
November 15, 2018 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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15130251 |
Apr 15, 2016 |
10151748 |
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16192160 |
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PCT/US2014/061230 |
Oct 17, 2014 |
|
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15130251 |
|
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61892274 |
Oct 17, 2013 |
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Current U.S.
Class: |
1/1 |
Current CPC
Class: |
C12Q 1/68 20130101; C12Q
1/68 20130101; G01N 33/5308 20130101; C12Q 2565/607 20130101; C12Q
2565/601 20130101; C12Q 2563/179 20130101; C12Q 2565/601 20130101;
C12Q 1/68 20130101 |
International
Class: |
G01N 33/53 20060101
G01N033/53; C12Q 1/68 20060101 C12Q001/68 |
Claims
1) A method of determining the structure of a molecule, comprising:
labeling a first location on the molecule with a first DNA strand;
measuring a force-time waveform using the twisting of a T-shaped
atomic force microscope cantilever scanning across the molecule,
wherein the cantilever includes a DNA probe having a first region
that is complimentary to the first DNA strand.
2) The method of claim 1, wherein the molecule is a protein.
3) The method of claim 1, wherein the molecule is one of a protein
complexed with DNA, a protein complexed with RNA, a protein
complexed with both DNA and RNA, a sugar or a lipid.
4) The method of claim 1, wherein labeling a first location further
comprises replacing a native amino acid located at the first
location with a first replacement amino acid and binding the first
DNA strand to the first replacement amino acid.
5) The method of claim 1, wherein labeling the first location
further comprises binding a biotin molecule to the first location,
and binding the biotin molecule to the first DNA strand.
6) The method of claim 1, further comprising labeling a second
location on the molecule with a second DNA strand; and wherein the
DNA probe includes a second region that is complimentary to the
second DNA strand.
7) The method of claim 6, wherein labeling a second location
further comprises replacing a native amino acid located at the
second location with a second replacement amino acid and binding
the second DNA strand to the second replacement amino acid.
8) The method of claim 6, wherein labeling the second location
further comprises binding a biotin molecule to the second location,
and binding the biotin molecule to the second DNA strand.
9) The method of claim 1, further comprising labeling a plurality
of locations on the molecule with a plurality of DNA strands, and
wherein the DNA probe has a complimentary region for each of the
DNA strands.
10) The method of claim 9, further comprising measuring pairwise
distances between each of the DNA strands.
11) The method of claim 10, further comprising determining a
three-dimensional structure based at least in part on the pairwise
distances.
12) The method of claim 1, wherein the first DNA strand is between
2 and 30-base-long single-stranded DNA.
13) The method of claim 1, wherein scanning comprises a fluid
tapping mode.
14) An atomic force microscope for determining the structure of a
molecule having a first location labeled with a first DNA strand,
comprising: a cantilever having a body having T-shaped geometry
including a base, a first end and a second end; a tip, disposed at
one of the first and second end; and a DNA probe, coupled to the
tip, and having a first region that is complimentary to the first
DNA strand.
15) The device of claim 14, wherein the body comprises silicon
nitride.
16) The device of claim 14, wherein the tip comprises silicon.
17) The device of claim 14, wherein the cantilever has a resonance
frequency between 4 and 1.20 MHz.
18) The device of claim 14, wherein the cantilever has a spring
constant of the vertical deflections between 35 pN/nm and 200
pN/nm.
19) The device of claim 14, wherein the cantilever has a spring
constant of torsional modes between 200 pN/nm and 400 pN/nm.
20) The device of claim 14, wherein the DNA probe includes a second
region that is complimentary to a second DNA strand coupled to a
second location on the molecule.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This application is a continuation of U.S. application Ser.
No. 15/130,251, filed Apr. 15, 2016, now allowed, which is a
continuation of PCT Application No. PCT/US2014/061230, filed on
Oct. 17, 2014, which claims priority to U.S. Provisional
Application Ser. No. 61/892,274, filed on Oct. 17, 2013, each of
which are incorporated by reference herein and from which priority
is claimed.
SEQUENCE LISTING
[0002] The specification further incorporates by reference the
Sequence Listing submitted herewith via EFS on Apr. 15, 2016.
Pursuant to 37 C.F.R. .sctn. 1.52(e)(5), the Sequence Listing text
file, identified as 070050.5696_SL, is 3,813 bytes and was created
Apr. 15, 2016. The Sequence Listing, electronically filed herewith,
does not extend beyond the scope of the specification and thus does
not contain new matter.
BACKGROUND
[0003] The disclosed subject matter relates to devices and methods
for determining molecular structure. Atomic force microscopy
provides for imaging utilizing measurements of force between a
probe and the surface of an object to be imaged. When the stylus is
brought into contact with the surface, it can become deflected by
forces in accordance with Hooke's Law. This deflection can be
measured and recorded, such that the atomic force microscope can
produce a 3-D surface map of the object under inspection.
[0004] Scanning probe microscopes (SPMs), for example, atomic force
microscopes, can allow imaging and chemical characterization of
surface down to the atomic scale. The localized tip-sample
interactions in SPMs limit high resolution images to the topmost
atomic layer of surface. Consequently, characterizing the 3-D inner
structure of materials and biomolecules can be difficult for
SPMs.
Scanning probe microscopes (SPM) can be operated in so-called
tapping mode, where the probe or stylus comes into intermittent
contact with the surface to be imaged. Operation in tapping mode
can avoid causing damage and prevent the probe from sticking to the
surface, while ensuring that the probe is close enough to the
surface to produce high quality images. The probe can be capable of
not only physically imaging the sample but identifying its
biochemical composition.
[0005] However, using a probe to obtain information about the
chemical identities of atoms and molecules on the Angstrom scale
can necessitate imaging modalities that operate under vacuum, which
can be ill-suited for biomolecules in a solution. Accordingly,
there exists a need for an improved imaging technique for
determining molecular structure.
SUMMARY
[0006] The disclosed subject matter provides devices and methods
for determining the structure of a molecule. In an exemplary
embodiment, a method of determining the structure of a molecule can
include labeling a first location on the molecule with a first DNA
strand. The method can include measuring a force-time waveform
using the twisting of a T-shaped atomic force microscope cantilever
scanning across the molecule. The cantilever can include a DNA
probe having a first region that is complimentary with the first
DNA strand.
[0007] In some embodiments, the molecule can be a protein. In some
embodiments the molecule can be one of a protein complexed with
DNA, a protein complexed with RNA, a protein complexed with both
DNA and RNA, a sugar or a lipid. Labeling a first location can
include replacing a native amino acid located at the first location
with a first replacement amino acid and binding the first DNA
strand to the first replacement amino acid. Labeling the first
location can also include binding a biotin molecule to the first
location, and binding the biotin molecule to the first DNA
strand.
[0008] In some embodiments the method can include labeling a second
location on the molecule with a second DNA strand. The DNA probe
can include a second region that is complimentary with the second
DNA strand. Labeling the second location can include replacing a
native amino acid located at the second location with a second
replacement amino acid and binding the second DNA strand to the
second replacement amino acid. Labeling the second location can
include binding a biotin molecule to the second location, e.g., the
biotin molecule can be bound to the second DNA strand.
[0009] In some embodiments, the method can include labeling a
plurality of locations on the molecule with a plurality of DNA
strands. The DNA probe can have a complimentary region for each of
the DNA strands. The method can include measuring pairwise
distances between each of the DNA strands. In some embodiments, the
method can include determining a three-dimensional structure based
at least in part on the pairwise distances.
[0010] In some embodiments, the first DNA strand can be between 2
and 30 base-long single-stranded DNA. Scanning can include a fluid
tapping mode.
[0011] According to another exemplary embodiment, an atomic force
microscope for determining the structure of a molecule having a
first location labeled with a first DNA strand is provided. In one
arrangement, the atomic force microscope can include a cantilever.
The cantilever can have a body having a T-shaped geometry including
a base, a first end and a second end. The cantilever can include a
tip, disposed at one of the first and second end. The cantilever
can include a DNA probe. The DNA probe can be coupled to the tip,
and have a first region that is complimentary to the first DNA
strand.
[0012] In some embodiments, the body can be silicon nitride. The
tip can be silicon. The cantilever can have a resonance frequency
between 4 and 1.2 MHz. The cantilever can have a spring constant of
the vertical deflections between 35 pN/nm and 200 pN/nm. The
cantilever can have a spring constant of torsional modes between
200 pN/nm and 400 pN/nm. In some embodiments the DNA probe can
include a second region that is complimentary to a second DNA
strand coupled to a second location on the molecule.
[0013] The accompanying drawings, which are incorporated in and
constitute part of this specification, are included to illustrate
and provide a further understanding of the method and system of the
disclosed subject matter. Together with the description, the
drawings serve to explain the principles of the disclosed subject
matter.
BRIEF DESCRIPTION OF THE FIGURES
[0014] FIG. 1 shows an exemplary method for determining the
structure of a molecule in accordance with the disclosed subject
matter.
[0015] FIG. 2 illustrates an atomic force microscope including a
cantilever in accordance with the disclosed subject matter.
[0016] FIG. 3A-FIG. 3F illustrate chemically-specific imaging and
3D reconstruction using DNA labels.
[0017] FIG. 4A and FIG. 4B illustrate locating specific chemical
targets with high spatial-resolution and reconstructing the 3-D
locations of targets from their pairwise distances.
[0018] FIG. 5A-FIG. 5E illustrate tuning the lifetime of DNA
interaction enhances target specificity
[0019] FIG. 6A-FIG. 6F illustrate imaging of DNA molecules
immobilized directly onto a substrate.
[0020] FIG. 7A-FIG. 7E illustrate chemically specific imaging and
3-D reconstruction in a protein complex.
[0021] FIG. 8A-FIG. 8C illustrate data related to the relative
positions of probe and target DNAs.
DETAILED DESCRIPTION
[0022] Devices and methods for determining the structure of a
molecule are disclosed herein. For example, the presently disclosed
subject matter can provide techniques to determine chemical
identities with Angstrom scale spatial resolution though the use of
a specially equipped atomic force microscope (AFM).
[0023] According to one aspect of the disclosed subject matter, a
method determining the structure of a molecule is provided. The
method can include chemo-mechanical labeling employing
single-stranded DNA to label target sites on a biomolecule. A
nanomechanical readout mechanism based on atomic force microscopy
can be used to locate the chemo-mechanical labels. The
chemo-mechanical labeling method can generate multi-color images
wherein the sequence of DNA encodes color information. The
disclosed subject matter can be utilized for chemically-selective
imaging to investigate single biomolecules with sub-molecular
chemical and structural detail. FIG. 1 shows, for the purpose of
illustration and not limitation, a method 100 for determining the
structure of a molecule in accordance with the disclosed subject
matter. The molecule can be a biomolecule, for example, a protein,
proteins in complex with RNA and/or DNA, or proteins in complex
with other proteins, lipids, or sugars. The method can include
labeling a first location on the molecule with a first DNA strand
(1). In some embodiments, the method can include labeling a second
location on the molecule with a second DNA strand. In some
embodiments, labeling the first and/or second locations can include
replacing a native amino acid with a first and second,
respectively, replacement amino acid bound to the first and second,
respectively, DNA strand. In some examples, a biotin molecule can
be used as a replacement amino acid at the first or second
location. In some embodiments, replacement amino acids can include
cysteine, lysine, and tyrosine. These amino acids can bind to DNA
that is modified specifically to these amino acids. The replacement
amino acids can be bound to the first or second DNA strand, and the
DNA strand can be used to label the first or second location,
respectively. For example, the disclosed subject matter can be
utilized to image the location of biotins bound to a single
streptavidin molecule. The first DNA strand and the second DNA
strand can be 6-base-long single stranded DNAs. The DNA strand can
range between a 1-base-long strand to a 30-base-long strand. In
some embodiments, the strands can be 15- or 9-base long single
stranded DNAs. In some embodiments the number of bases can be
selected based on the resonance frequency of the cantilever.
[0024] The method can include measuring a force-time waveform using
the twisting of a T-shaped atomic force microscope cantilever
scanning across the molecule (2). It some embodiments the method
can use any known technique for using an atomic force microscope to
measure force-time waveforms. The cantilever can include a DNA
probe having a first region that is complimentary with the first
DNA strand. In some embodiments, the probe can have a second region
that is complimentary with the second DNA strand.
[0025] In some embodiments, scanning can include a fluid tapping
mode. Fluid tapping mode includes vibrating the cantilever and
adjusting the relative position of the cantilever to the surface
under feedback control so that the vibration amplitude remains
constant. Alternatively, the feedback can include measurement of
the peak tapping force and keeping it constant.
[0026] In an exemplary embodiment of the disclosed subject matter,
an AFM for determining the structure of a molecule having first and
second locations labeled with first and second DNA strands is
provided. Referring to FIG. 2, for the purpose of illustration and
not limitation, the device 200 can include an atomic force
microscope 211 (illustrated as a box) which can include a
cantilever 205. The atomic force microscope can utilize cantilevers
205 with a custom geometry, including a body and a wider region at
the free end. For example, the cantilever can have a body 206
having a T-shaped geometry. The T-shaped geometry can include a
base 207, a first end 208, and a second end 209. The first 208 and
second 209 ends can have a width of about 100 .mu.m, and can be,
for example about 60 .mu.m. In some embodiments the first 208 and
second 209 ends can have a width of 10 .mu.m. The body 206 can be
silicon nitride. The body 206 can be other materials, for example
silicon.
[0027] The cantilever 205 can also include a tip 210. The tip 210
can be disposed on one of the first end 208 and second end 209. The
tip 210 can be silicon.
[0028] The device 200 can include a DNA probe 201 coupled to the
tip 210. The DNA probe 201 can include a first region 201a. The
first region 201a can be complimentary with a first DNA strand 202
coupled to a first location on molecule 204. In some embodiments,
the DNA probe 201 can include a second region 201b. The second
region 201b can be complimentary with a second DNA strand 203
coupled to a second location on molecule 204. In some embodiments
the DNA probe can have additional regions that can be complimentary
to additional DNA strands coupled to molecule 204.
[0029] In some embodiments, the cantilever can have a resonance
frequency between 4 and 1.2 MHZ. The cantilever can have a spring
constant of the vertical deflections between 35 pN/nm and 200
pN/nm. The cantilever can have a spring constant of torsional modes
between 200 pN/nm and 400 pN/nm.
[0030] According to another aspect of the disclosed subject matter,
an atomic force microscope can operate by measuring forces between
biomolecules and how these forces change over time or distance. The
disclosed subject matter provides for the conversion of chemical
information into a time or distance signal, which can be measured
by the atomic force microscope. The disclosed subject matter also
provides techniques for encoding and decoding information in energy
landscapes of single biomolecular interactions. This can be
accomplished by designing DNA molecules that can hybridize to
multiple targets, each creating a distinct force-extension curve
and having a lifetime tuned to the resonance frequency of an atomic
force microscope cantilever. The disclosed subject matter also
provides techniques for generating multicolor images of distinct
DNA molecules with a resolution greater than 1 nm. Referring to
FIG. 3, for the purpose of illustration and not limitation, FIGS.
3A-3C illustrate chemically-specific imaging and 3-D reconstruction
using DNA labels. A strand of DNA, the probe 201, can interact with
target DNA strands having shorter sequences 202, 203. The DNA
strands 202, 203, can be coupled to a molecule 204 at known
locations. Sequences of the target DNA strands can be complementary
to different regions along the probe DNA 201. For example, region
201a can be complementary with DNA strand 202 and region 201b can
be complementary with DNA strand 203. Formations of duplexes can
create distance force-time waveforms, which can be detected by the
twisting of T-shaped AFM cantilevers 205. For example, the pulling
forces exerted by the target molecules can appear as negative peaks
in the force-time waveforms. FIGS. 3D-3F show examples of
experimentally measured waveforms corresponding to FIGS. 3A-3C,
respectively. Mapping the timing of pulling events across the
sample surface can allow locating specific chemical targets with
high spatial resolution (for example as illustrated in FIG. 4A)
and/or reconstructing the 3-D locations of targets from their
pairwise distances (for example as illustrated in FIG. 4B).
Example 1
[0031] In accordance with the disclosed subject matter, imaging and
three-dimensional reconstruction of chemical groups inside a
protein complex using atomic force microscopy is demonstrated.
Short single-stranded DNAs can be employed as imaging labels linked
to target regions inside a protein complex. T-shaped AFM
cantilevers functionalized with complementary probe DNAs can allow
locating the labels with sequence specificity and sub-nanometer
resolution. After measuring pairwise distances between labels, the
3D structure formed by the target chemical groups within the
protein complex can be reconstructed using geometric calculations.
Examples with biotin-streptavidin complex showed that the predicted
3-D loci of the carboxylic acid groups of biotins were within
2-Angstroms of their respective loci in the corresponding crystal
structure. Therefore, scanning probe microscopes can complement
certain structure biological techniques in solving structures that
are difficult to study due to their size and complexity.
[0032] The temporal characteristics of dynamic tip-sample
interactions can be utilized to image material properties with high
spatial resolution. The ability to probe interaction forces with
good time resolution can also lead to detecting short-lived
biomolecular interactions and harnessing them for chemically
specific imaging purposes. For example, short-single-stranded DNA
molecules can be used as labels attached to target chemical groups
within biomolecules to allow chemically specific imaging and 3-D
reconstruction.
[0033] Referring again to FIGS. 3 and 4, FIG. 3 illustrates how
sequence dependent binding geometries of DNA can allow detecting
and discriminating DNA sequences from the temporal characteristics
of the forces measured by the AFM 200. The molecular configuration
of the probe 201 and targets facilitate the rupture of the orange
duplex to be delayed because the single-stranded green region 202
has to be stretched first. This labelling strategy can be used to
image chemical groups within biomolecular complexes and reconstruct
their 3-D locations (FIGS. 4A, 4B).
[0034] Partial hybridization of DNA can create complications. Any
unpaired base can increase the length of the region that requires
stretching, which can make it difficult to rely on rupture times to
discriminate DNA sequences. (As used herein, rupture time is
defined relative to the beginning of cantilever oscillation period,
which is when the tip is at its highest position.)
[0035] The role of partial hybridizations can be minimized by
taking advantage of their reduced lifetimes relative to fully
hybridized DNAs. FIG. 5A depicts, for the purpose of illustration
and not limitation, an approximate trend of duplex DNA lifetimes.
If the lifetime of the partially hybridized DNA were longer than
the experiment duration, the measurements would incorporate events
that belong to partial hybridizations. However, by choosing a
sufficiently short length of DNA, the lifetime of partially
hybridized interactions can be kept below the experiment duration,
which can minimize the spread of detected rupture times. FIG. 5B
illustrates a reduction in the spread of rupture times for 15-, 9-,
and 6-base long DNA.
[0036] Referring again to FIG. 3, the probe 201 can be a 12-base
probe DNA, and target strands 202, 203 can be 6-base complementary
target DNAs. For example, one can have a sequence A.sub.6 and the
other can have the sequence G.sub.6. In some embodiments, any
sequence can be used, as long as there is a complimentary region on
the probe 201.
[0037] In a first embodiment, targets can be directly attached to a
substrate and not to other biomolecules. Rupture times measured on
a A.sub.6-only surface (FIG. 5C) and on a G.sub.6-only surface
(FIG. 5D) show that the measured distributions are located in
temporally distinct regions of the oscillation period. Furthermore,
on a surface with both A.sub.6 and G.sub.6, the distribution of
rupture times reproduced a superposition of the original peaks
(FIG. 5E). These observations demonstrate the ability to rely on
rupture times to discriminate short target DNAs.
[0038] In an exemplary embodiment, rupture forces (FIG. 6B) and
rupture times (FIG. 6C) can be recorded across a sample of DNA
targets immobilized directly onto a substrate, this time with
sequences C.sub.6 and T.sub.6. Locations where rupture forces
exceeded the noise threshold value of 39 pN were identified and
then corresponding rupture times were examined to determine whether
the observed events belong to the targets. FIG. 6D illustrates the
resulting multicolor image, which exhibits rupture events that are
separated from their nearest neighbors by 0.2 nm to 10 nm. Several
pixels appear as clusters. The clusters can allow estimating the
resolution limit and localization accuracy of the imaging
system.
[0039] FIG. 6E illustrates a plot of the distribution of distances
from nearest neighbors. The histogram shows that nearly half of the
detected events are within less than 1 nm distance. The remaining
events exhibit a distribution that closely matches the probability
distribution function p(x) corresponding to randomly located
particles, p(x)=2.pi..lamda.xe.sup.-.pi..lamda.x.sup.2 where
.lamda. corresponds to particle density and x corresponds to
particle spacing. The observation can suggest that clustering is
not random and comes from repeated measurements of the same target.
(The possibility of multiple probes interacting with targets can be
ruled out. For this to explain clustering, probes have to be less
than 1 nm apart.)
[0040] Statistical analysis of clusters can provide calculable
information about the resolution limit and the accuracy of the
color assignments. Because clusters originate from repeated rupture
events of the same target DNA, the special extents observed in the
ensemble of clusters (FIG. 6F) represent the point spread function
(PSF) of the imaging system whose full width at half maximum (FWHM)
corresponds to the resolution limit. The PSF can be approximated
with a Gaussian profile and the variances (.sigma..sup.2)
calculated for each cluster can be averaged to estimate the
root-mean-square size of the PSF (.sigma.), which can be related to
the limit of resolution (FWHM.about.2.4 .sigma.). Along the
horizontal and vertical directions, resolution limits can be
estimated as 0.47 nm (.sigma.=0.20 nm) and 0.58 nm (.sigma.=0.24
nm), respectively. In addition, the localized accuracy (given with
.sigma./N.sup.1/2), where N is the number of rupture events in a
cluster) is better than 0.25 nm (note that the positioning accuracy
of the piezoelectric scanner is not included in this estimate). The
extremely small limit of resolution is attributed to small sizes of
the probe and target molecules. The contour length of a 6-base long
DNA strand (.about.3.8 nm) is comparable to its persistence length
(2 to 3 nm), which can limit the reach of the probes and
targets.
[0041] The color uniformity of clusters can allow estimating the
accuracy of color assignments. About 88% of the 299 clusters were
completely T.sub.6 or C.sub.6 and only .about.4.3% had equal number
of T.sub.6 and C.sub.6. The strong correlation between color
assignments within a cluster can suggest that interactions between
the probe and target DNAs are detected with sequence specificity.
Varying the tip and sample combinations can verify the
repeatability of color uniformities seen in clusters, as well as
the resolution limits estimated from the physical sizes of
clusters.
[0042] The clusters in FIG. 6F are predominantly horizontal. A
reason can be the raster scan pattern of the AFM. While the
scanning tip moves continuously in the horizontal direction, it can
make discrete steps in the vertical direction. If considering two
cases where a target molecule is located halfway between the
centers of pixels in the horizontal and vertical directions, the
one in the horizontal direction is more likely to be detected
because the tip will gradually move over it. Furthermore, this
target is likely to be detected as a cluster by appearing in the
two adjacent horizontal pixels. In the case of the target located
halfway between pixels in the vertical direction, the tip will skip
the target as it moves from one scan line to the next. This can
lower the probability of the target being detected in the adjacent
vertical pixels.
[0043] In an exemplary embodiment, devices and methods of the
disclosed subject matter were used to locate chemical groups within
single biomolecules by attaching 6-base-long single-stranded DNAs
to target chemical groups. Biotin-streptavidin complexes were used.
Streptavidin has four binding sites for biotin. Due to the symmetry
of the crystal structure, the distances between pairs of carboxylic
acids (the sites where DNA labels are linked to biotins) can have
three distinct values (FIGS. 7A, 7B). As a result, carboxylic acids
of biotins form a tetrahedron with opposite edges having equal
length.
[0044] FIGS. 7C and 7D show grayscale height images of streptavidin
complexed with DNA-labelled biotins, with the locations of detected
rupture events highlighted with color. A set of 12 additional
images are given in FIG. 7E. Similar to the results in FIG. 6D,
clustering of rupture events was observed. The clusters are
predominantly composed of single colors, suggesting that color
assignments are accurate even when targets are bound to proteins.
Although one DNA sequence is sufficient to label biotins, two
sequences were used to test if sequences can be discriminated
reliably when targets are bound to proteins, which can help with
studies of more complex systems.
[0045] The images in FIG. 7C-E typically show two distinct
locations for rupture events despite the four binding sites of
streptavidin. This is because only those label DNAs that are
oriented towards the tip are likely to bind. Label DNAs that are
oriented towards the substrate have to bend in order to hybridize
with the probe DNA, which can reduce their binding probability.
[0046] The distance values between the pairs of rupture locations
seen in each image exhibit clustering around two values: 5.3 nm and
6.0 nm (FIG. 8A). A less prominent clustering is seen around 3.0
nm. Proceeding with the assumption that these three values reflect
the distances between the midpoints of label DNAs, (this would be
the approximate configuration that requires the least amount of
bending energy, as illustrated in FIG. 8C), shape of the
tetrahedron whose corners correspond to the midpoints of DNA was
determined by solving algebraic equations satisfied by the
coordinates of the corners. The locations of carboxylic acids were
estimated by translating the corners of the tetrahedron towards its
center of mass by a distance equal to 11 Angstroms (approximate
length of 3 base long duplex DNA). The new coordinates represent
the predicted 3-D locations of the carboxylic acids relative to
each other. These geometrical calculations involve a number of
assumptions.
[0047] First, the label-DNAs would orient approximately normal to
the surface of the protein due to electrostatic repulsion and that
surface normal can be approximated with the radial line pointing
away from the center of mass. Any errors due to deviations from
this approximation can be small because of the short length of the
3-base long duplex DNA. Additionally, it was assumed that the
6-carbon aliphatic linker that connects DNA to carboxylic acid
would orient approximately in the direction of the carbons C1 and
C3 of the biotin (C1 belongs to the carboxylic acid. C2 was skipped
to account for bond angles in the carbon chain). This direction is
approximately orthogonal to the radial line from the center of
mass, hence does not contribute to the radial position of labels in
a significant way. Furthermore, deformations of the molecular
complex under the applied force were neglected because the peak
tapping forces were limited to 10 pN.
[0048] FIG. 8B shows a comparison of the predicted locations of
carboxylic acids, represented with yellow spheres, with the crystal
structure of the biotin-streptavidin complex. The carboxylic acids
in the crystal structure are located at the Y-shaped ends of the
red colored biotins. To make this comparison the center of masses
of the predicted 3-D geometry and the crystal structure were
aligned, and then two of the carboxylic acids in the crystal
structure (carbon in the carboxylic acid of the biotins) were used
as reference points to orient the predicted geometry such that the
distance between the two references and their two counterparts in
the predicted geometry are minimized. As seen in FIG. 8B, despite
the approximations, there is a good degree of agreement, within 2
Angstroms, between the predicted locations with their counterparts
in the crystal structure. This demonstrated capability of
determining 3-D locations of chemical groups in biological
macromolecules underscores the need for scanning probe microscopes
in structural biology where large biomolecular complexes can pose
challenges to certain technologies.
[0049] In certain embodiments of the disclosed subject matter,
cantilevers with a custom T-shaped geometry can be used, and are
commercially available from, for example, Applied Nanostructures,
Inc. Santa Clara, Calif. and Bruker-Nano, Santa Barbara, Calif. The
body of cantilevers can be made of silicon nitride and the tip can
be made of silicon. The resonance frequencies of the cantilevers in
solution can be between 4 and 1.2 MHz as determined from thermal
noise spectrum. The spring constant of the vertical deflections
range can be from 35 pN/nm to 200 pN/nm, each calibrated against
the thermo-mechanical noise.
[0050] The spring constants of the torsional modes (200 pN/nm-400
pN/nm) can be calibrated against the thermal noise spectrum of
torsional deflections. This calculation requires the knowledge of
tip offset distances, which can be determined using scanning
electron microscopy. There can be variations in resonance
frequencies and spring constants, because cantilevers with
different lengths can be used. Longer cantilevers can provide a
better time resolution due to higher ratio of torsional to flexural
resonance frequencies (.about.13.5) compared to the shorter
cantilevers (.about.7). Cantilevers can have a length between 300
.mu.m and 10 .mu.m. The shorter cantilevers can provide improved
signal to noise ratio, but they underestimate the magnitude of
rupture forces due to filtering.
[0051] The tips can be cleaned by immersing cantilevers into an
acidic solution (nitric acid/H2O, 1:2) for 20 min. After rinsing
with de-ionized water, the tips can be dried overnight under
nitrogen atmosphere. To generate amino-groups, the cleaned tips can
be placed in an anhydrous toluene solution containing 1% APDES
(e.g., 3-aminopropyl diethoxymethyl silane, commercially available
from, for example, from Gelest) for 3 hours and under nitrogen
atmosphere. After the reaction, the tips can be rinsed with toluene
gently and then baked at 95.degree. C. for 30 min. Then the tips
can be washed with toluene, methanol, and de-ionized water
sequentially. The resulting amino-functionalized tips can be dried
in a chamber under nitrogen atmosphere.
[0052] Next, heterofunctional crosslinkers such as SM (PEG).sub.2
(N-hydroxysuccinimidyl-(ethylene glycol)2-maleimide), commercially
available from, for example, Thermo Scientific, which contains
maleimide and N-hydroxysuccinimide (NHS) groups at its ends via two
ethylene glycol repeats, can be allowed to the tips to generate
maleimide-functionalized surface. The tips can be placed in a
crosslinker solution (1 mg in 100 .mu.L of phosphate buffered
saline (PBS) (pH 7.4)) and incubated for 90 min. After the
reaction, the tips can be rinsed with a PBS buffer, e.g., dimethyl
sulfoxide (DMSO), for example, methoxy sulfide, commercially
available from, for example, Sigma Aldrich, de-ionized water
sequentially. Finally, DNA molecules can be immobilized on the
surface by placing the tips in a thiolated oligonucleotide
solution, commercially available from, for example, Integrated DNA
Technologies, Inc., as a 10 .mu.M in PBS, overnight. After the
incubation, the tips can be washed with PBS and de-ionized
water.
[0053] Note that the tip functionalization method does not ensure
that there will be a single DNA probe at the tip. However, due to
the small sizes of probes and targets, probes that are further away
from the very end of tip can have a lower probability of binding.
There can be an energy barrier imposed by the stretching of the
probe, which will reduce binding probability.
[0054] A silicon wafer can be used as a substrate. The identical
cleaning and modification procedures as tip functionalization can
be applied. To create samples with mixed target sequences, the
final concentration of each DNA sequence can be adjusted to 5 .mu.M
or 10 .mu.M (FIG. 3d). After preparation, the substrate can be
mounted on an AFM sample stage for imaging. Imaging can be
performed in PBS (pH 7.4).
[0055] DNA-bound biotin-streptavidin sample preparation will next
be described. A stock solution of streptavidin (available from
Sigma Aldrich) in 1 mg ml-1 PBS (pH 6.8) can be made and can be
diluted with PBS (pH 6.8) to a final concentration of 0.1 mg mL-1
for each experiment. A 60 uL of the diluted solution can be dropped
onto a freshly cleaved mica surface (available from VWR). After 1
hour, the mica surface can be washed with PBS (pH 6.8) and
subsequently incubated overnight in a solution containing DNA
targets modified with a biotin at its 5' end (source: Integrated
DNA technologies, Inc., 10 .mu.M for each target in PBS (pH 6.8)).
After the incubation, the surface can be washed with PBS (pH 6.8)
and mounted on the AFM sample stage for imaging. Imaging can be
performed in PBS (pH 6.8).
[0056] AFM testing with two commercial AFM systems, BioScope II and
Multimode V, Bruker-Nano, Inc., were performed. Imaging can be
carried out in fluid tapping mode at room temperature (20.degree.
C.). Torsional deflection signals from T-shaped cantilevers can be
analyzed in real time to create rupture force and rupture time
maps. Rupture force is defined as the minimum value (most negative)
of the tip-sample force waveform. Rupture time is defined as the
temporal location of the minimum force value within a single
oscillation period. The highest point of the tip determines the
beginning and the ending of the period. The analysis can be carried
out in Labview (available from National Instruments) with a
computer equipped with a data acquisition card, such as the
NI-56115. The NI-56115 card can have a sampling rate of 10 MHz. In
some embodiments, other sampling cards with a sampling rate above
400 KHz can be used.
[0057] Algorithms can be used to calculate tip-sample force
waveforms. During the imaging the drive amplitudes can be adjusted
to maintain peak tapping forces to be below 10 pN, which can be
expected to minimize the deformations of the protein surface. The
set-point amplitudes can be selected according to the length of DNA
molecules. For the experiments in FIG. 5, to account for
differences in contour lengths of 6-, 9-, and 15-base long DNA, the
peak-to-peak oscillation amplitudes can be adjusted in proportion
to the number of bases and approximately equal to twice the contour
length of hybridized DNA. A 0.63 nm/base can be used to approximate
the contour length. For multicolor imaging, the set-amplitude value
can be maintained at approximately 4 nm. The immobilized DNA
surface can be imaged with a scan speed of 400 nm/sec. In the case
of imaging streptavidin molecules complexed with biotinylated DNA,
scan speeds around 600 to 1000 nm/sec can be used.
[0058] To identify the locations of rupture events, a threshold
force level beyond which a measured pulling force is considered as
a rupture event between the complementary probe and target. For
this, one can compared force histograms recorded on fully
complementary targets and non-complementary targets and select the
value beyond which the events counted on non-complementary surface
is less than 5% of the events counted on complementary DNA surface.
The resulting error rate of 5% represents a compromise for
minimizing false positives (selectivity) and false negatives
(sensitivity).
[0059] The threshold values were 12-14 pN for FIGS. 5 and 39-49 pN
for FIG. 7. The limited torsional bandwidth of the shorter T-shaped
cantilevers used in the experiments underestimate the rupture
forces. Because binding probability of probe and targets are low,
one can incorporate rupture data from trace and retrace images into
a single image for experiments on immobilized DNA samples. For DNA
labels bound to biotin-streptavidin complexes, one can use trace
and retrace images separately. By comparing the locations of the
rupture events in trace and retrace images on DNA surfaces, it was
found that approximately 50% of the events overlap (within 2 nm)
with a rupture event in the other image. This suggests that
detecting a single label in a single image is about 50%. Therefore
combining rupture data from both images can allow detecting a
majority of the labels.
[0060] To determine whether a detected rupture event corresponds to
one or the other target, one can looked at the rupture time. The
length of the entire period was defined as 64 units (ranging from
-32 to 32, with zero corresponding to the lowest point of the tip).
Based on the results in FIG. 5(c-e), rupture events between -10 and
10 can be counted as the target complementary to the base region of
the DNA probe and events between 18 and 32 are counted as the
target that complementary to the free end of the DNA probe. Once
the target is determined, a color-coded image can be generated.
[0061] With the immobilized DNA samples, one can determine clusters
in rupture events and characterized the spread of the each cluster.
Clusters can be defined such that a given pixel representing a
rupture event belongs to a cluster if at least one of the elements
of the cluster is within 0.68 nm (3.5 pixels). This threshold can
be determined by a histogram, as illustrated in FIG. 6e. With this
algorithm 299 clusters were identified. The variances in horizontal
and vertical directions can be calculated for each cluster using
sample means. For clusters with more than two elements, the
computer picked two elements randomly. The resulting variance can
be averaged over the entire set of clusters. If a cluster has
elements only in the same row or column, its variance is not
included in the calculations for the orthogonal direction. With the
biotin-streptavidin complexes, the distances between the rupture
locations can be analyzed. In case of clustered pixels, one can
assume the rupture location is at the center of mass of the
cluster. Rupture signals that fall outside of the boundaries of
streptavidin can be ignored, as these can be caused by force noise
or unspecific interactions. Pairwise distance data can be analyzed
by calculating the density of data points as a function of
distance. A moving window that is 0.5 nm wide can be used in the
density calculations.
[0062] Probe and target DNA sequences are provided in Table 1.
TABLE-US-00001 TABLE 1 Probe and target DNA sequences Probe
Target(s) FIG. 5B (15-bp) 5'-SH-ACC TGA 5'-SH-AAA CCC CCC GGG
TTT-3' GGG TCA GGT-3' FIG. 5B (9-bp) 5'-SH-CCC GGG 5'-SH-AAA CCC
TTT-3' GGG-3' FIG. 5B (6-bp) 5'-SH-GGG TTT-3' 5'-SH-AAA CCC-3' FIG.
5C-E 5'-SH-TTT TTT 5'-SH-AAA AAA-3' CCC CCC-3' 5'-SH-GGG GGG-3'
FIG. 6D 5'-SH-AAA AAA 5'-SH-TTT TTT-3' GGG GGG-3' 5'-SH-CCC CCC-3'
FIG. 7 5'-SH-AAA AAA 5'-biotin-TTT GGG GGG-3' TTT-3' 5'-biotin-CCC
CCC-3'
[0063] While the disclosed subject matter is described herein in
terms of certain exemplary embodiments, those skilled in the art
will recognize that various modifications and improvements can be
made to the disclosed subject matter without departing from the
scope thereof. Moreover, although individual features of one
embodiment of the disclosed subject matter can be discussed herein,
or shown in the drawing of one of the embodiments and not in
another embodiment, it should be apparent that individual features
of one embodiment can be combined with one or more features of
another embodiment or features from a plurality of embodiments.
Thus, the foregoing description of specific embodiments of the
disclosed subject matter has been presented for purposes of
illustration and description. It is not intended to be exhaustive
or to limit the disclosed subject matter to those embodiments
disclosed.
Sequence CWU 1
1
15115DNAArtificial SequenceDescription of Artificial Sequence
Synthetic probe 1acctgacccg ggttt 1529DNAArtificial
SequenceDescription of Artificial Sequence Synthetic probe
2cccgggttt 936DNAArtificial SequenceDescription of Artificial
Sequence Synthetic probe 3gggttt 6412DNAArtificial
SequenceDescription of Artificial Sequence Synthetic probe
4ttttttcccc cc 12512DNAArtificial SequenceDescription of Artificial
Sequence Synthetic probe 5aaaaaagggg gg 12612DNAArtificial
SequenceDescription of Artificial Sequence Synthetic probe
6aaaaaagggg gg 12715DNAArtificial SequenceDescription of Artificial
Sequence Synthetic oligonucleotide 7aaacccgggt caggt
1589DNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 8aaacccggg 996DNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 9aaaccc 6106DNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 10aaaaaa
6116DNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 11gggggg 6126DNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 12tttttt 6136DNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 13cccccc
6146DNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 14tttttt 6156DNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 15cccccc 6
* * * * *