TOWARDS Electronic Detection of Genomic-length DNA with no ... · e-mail: [email protected]...
Transcript of TOWARDS Electronic Detection of Genomic-length DNA with no ... · e-mail: [email protected]...
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TOWARDS Electronic Detection of Genomic-length DNA with no labels
Bob Austin, Princeton University and Visiting Fellow, Hong Kong University Science and Technology Institute for Advanced Studies
Chih-kuan Tung, Dept.of Physics, Hong Hong Kong University Science and Technology
Robert Riehn, Dept. Physics, North Carolina State University
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Outline:
1) The importance of single cell large scale genomic length mapping
2) Troubles with present single cell technologies
3) The advantages of nanochannels for large scale genomic length mapping
4) Beyond optics: electronic detection?
5) Quo vadis?Monday,11 May, 09
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1) The importance of single cell large scale genomic length mapping
“All happy families are the same, all unhappy families are unhappy in different ways”
-Tolstoy
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Reproduced with permission of the copyright owner. Further reproduction prohibited without permission.
WORLD WAR ON CANCER MAKES NOTABLE GAINSBy GEORGE A. SOPER, Ph.D.New York Times (1857-Current file); Dec 8, 1929; ProQuest Historical Newspapers The New York Times (1851 - 2003)pg. XX13
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My sister, Linda, died from ovarian cancer. The progression was typical: surgery, chemo, remission followed by relapse after 2 years, which was fatal. Same old story.
What happened to the War on cancer? Where is the Victory?
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The genome in cancer cells undergoes rapid evolution under conditions of high stress.
Sequencing is hopelessly specific for mapping these rapid and large scale genomic rearrangements, and present techniques cannot map single cells rapidly and with high spatial resolution.
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2) Troubles with present technologies
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© 2003 Nature Publishing Group
NEWS & VIEWS
ROBERT AUSTIN is at the Department of Physics,Jadwin Hall,Princeton University,Post Office Box 708,Princeton,New Jersey 08544-0708,USA.
e-mail: [email protected]
B ionanotechnology has become a hot area ofresearch as scientists struggle to applynanotechnology to areas of biologicalinterest.One of the main reasons for this isthe realization that nanotechnology can,in
principle,be used to examine biomolecules one by one.Achieving single-molecule analysis would have a hugepay-off.For example,single-molecule DNA sequencingmeans reading the base-pair sequence of a single DNAmolecule from a single cell without any of the enormouscomplications and information distortions created bythe existing steps of cloning,polymerase chain reactionamplification,and capillary electrophoresis separation.Unfortunately,analysing single molecules is a fiendishlydifficult task,not only because the individual moleculesmust be moved past a sensor of some sort,but alsobecause extraordinarily sensitive technologies must bedeveloped to respond to their molecular properties.
On page 611 of this issue,Li et al.1 exploit recentadvances in the fabrication of synthetic nanopores2,3
with remarkably small diameters (3–10 nm) to measurethe motion of single DNA molecules through the pores.The most surprising result of this work is that the DNAmolecules do not thread meekly through thesenanopores like a noodle of spaghetti that you suck up,but instead come through the pore in several ‘benthairpin’configurations.The experiments of Li et al. usereal molecules of biological interest,and are animportant step in crossing the gap between the quirkybut ‘true’nanopores of biology,and the robust,but stilltoo large,nanopores coming from physics.
Single-molecule sequencing is still a distant goal, sobefore they can address biologically relevant problems,scientists first need to learn how to handle single DNAmolecules.DNA can be an extremely long polymer,upto several centimetres in length.But as it has to curl upinto the nucleus of a cell (a few micrometres indiameter), it cannot be perfectly rigid.The ‘bendability’of a linear polymer can be expressed by a physical lengthcalled the persistence length — a concept that comes
from statistical physics,and is a measure of how far youcan go in a straight line along the backbone of apolymer,on average,before thermal fluctuations moveyou in another direction.A more accurate statement isthat the persistence length is the mean radius ofcurvature of the molecule at some temperature,T,due
nature materials | VOL 2 | SEPTEMBER 2003 | www.nature.com/naturematerials 567
NANOPORES
The art of sucking spaghettiBiomolecules are notorious for their unpredictable flexibility.Some of the smallest nanopores ever created are beingused to manipulate individual DNA molecules, with far-fromsimple results.
Figure 1 Scientists wishing to straighten out elastic polymers,such as DNA, require very tiny pores a fewnanometres in diameter.Li et al.1 use an ion beam to shrink a micropore in a silicon nitride membrane down tonanoscale dimensions.DNA molecules threading through the nanopores don’t always behave as expected,but these experiments bring us a step closer to the goal of single-molecule analysis, including DNA sequencing.
Image:Dana Sigall,www.sigall.com.
© 2003 Nature Publishing Group
NEWS & VIEWS
ROBERT AUSTIN is at the Department of Physics,Jadwin Hall,Princeton University,Post Office Box 708,Princeton,New Jersey 08544-0708,USA.
e-mail: [email protected]
B ionanotechnology has become a hot area ofresearch as scientists struggle to applynanotechnology to areas of biologicalinterest.One of the main reasons for this isthe realization that nanotechnology can,in
principle,be used to examine biomolecules one by one.Achieving single-molecule analysis would have a hugepay-off.For example,single-molecule DNA sequencingmeans reading the base-pair sequence of a single DNAmolecule from a single cell without any of the enormouscomplications and information distortions created bythe existing steps of cloning,polymerase chain reactionamplification,and capillary electrophoresis separation.Unfortunately,analysing single molecules is a fiendishlydifficult task,not only because the individual moleculesmust be moved past a sensor of some sort,but alsobecause extraordinarily sensitive technologies must bedeveloped to respond to their molecular properties.
On page 611 of this issue,Li et al.1 exploit recentadvances in the fabrication of synthetic nanopores2,3
with remarkably small diameters (3–10 nm) to measurethe motion of single DNA molecules through the pores.The most surprising result of this work is that the DNAmolecules do not thread meekly through thesenanopores like a noodle of spaghetti that you suck up,but instead come through the pore in several ‘benthairpin’configurations.The experiments of Li et al. usereal molecules of biological interest,and are animportant step in crossing the gap between the quirkybut ‘true’nanopores of biology,and the robust,but stilltoo large,nanopores coming from physics.
Single-molecule sequencing is still a distant goal, sobefore they can address biologically relevant problems,scientists first need to learn how to handle single DNAmolecules.DNA can be an extremely long polymer,upto several centimetres in length.But as it has to curl upinto the nucleus of a cell (a few micrometres indiameter), it cannot be perfectly rigid.The ‘bendability’of a linear polymer can be expressed by a physical lengthcalled the persistence length — a concept that comes
from statistical physics,and is a measure of how far youcan go in a straight line along the backbone of apolymer,on average,before thermal fluctuations moveyou in another direction.A more accurate statement isthat the persistence length is the mean radius ofcurvature of the molecule at some temperature,T,due
nature materials | VOL 2 | SEPTEMBER 2003 | www.nature.com/naturematerials 567
NANOPORES
The art of sucking spaghettiBiomolecules are notorious for their unpredictable flexibility.Some of the smallest nanopores ever created are beingused to manipulate individual DNA molecules, with far-fromsimple results.
Figure 1 Scientists wishing to straighten out elastic polymers,such as DNA, require very tiny pores a fewnanometres in diameter.Li et al.1 use an ion beam to shrink a micropore in a silicon nitride membrane down tonanoscale dimensions.DNA molecules threading through the nanopores don’t always behave as expected,but these experiments bring us a step closer to the goal of single-molecule analysis, including DNA sequencing.
Image:Dana Sigall,www.sigall.com.
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A very important concept here: the persistencelength "p" of a flexible polymer. Basically, it is ameasure of how far you move along an arc beforethermal energy bends the polymer randomly.
t(0)
t(s)
<t(0) t(s)> = exp(-s/p) p = 600 Angstroms =200 bp (double-strand DNA)
This number controls statistics, dynamics
movie:wayne
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Can you see the problem?
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Dekker et al. Notice the magic.Monday,11 May, 09
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3) The advantages of nanochannels for large scale genomic length mapping
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Here’s an interesting polymer problem: what happens when you put a long polymer of persistence length p in a nanochannel? Lot’s of surprises.
Suppose the channel is say 200 nm wide, and the polymer has a persistence length of 50 nm. The diameter of the dsDNA molecule is only about 2 nm, so most of the volume of the channel is water, since the diameter of the polymer is much less than the persistence length or the channel dimension.
You might think that the self-avoiding random walk would be an unnecessary complication.
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Lz = L(pw)1/3
D2/3
If the polymer has contour length L, the end-end length in a tube of diameter D for a polymer of width w is:
The entropic spring constant k of this confined polymer is:
k ! 154kBTL
!1
pwD
"1/3
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Lz = Lcos(θ) = L
!1!A
"DP
#2/3$
.
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Restriction mapping of DNA with endonucleases is a central method of modern molecular biology. It is based on the measurement of fragment lengths after digestion, while possibly maintaining the respective order.
Robert Riehn decided that perhaps we could bring restriction enzymes into these nanochannels and cut genomic length DNA molecules at precise sites. Since we would observe the cutting directly, there would be no scrambling of the order of the cut sites, and so we could do a direct physical map of a DNA of genomic length.
This has been a hard road to go down!
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4) Beyond optics: electronic detection
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Central idea: combine nanochannel elongation with “electronic” detection of the charged DNA molecule, either by nanoelectrodes directly put into nanochannels or via nanpores serially connected with nanochannel.
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Some warnings:
1) Debye length (shielding of charged phosphate groups by saline counter-ions is quite small (nm or less), creates charge double-layer.
1!
=
!""okBT
e2!ic!i z2i
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2) Water is a very wide band-gap semiconductor, “conduction” is via
electrochemical ion neutralization (something the cold-fusion people have trouble with I think)
so: impedance is strictly capacitively coupled through the double-layer unless electrode potential reaches hydrolysis potential.
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3) On-chip electronics (MOSFET?) probably needed for signal amplification/filtering/multiplexing cannot withstand high temperature processing/high field sealing technologies, we need to develop “soft” nanochannel techniques.
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One of my Princeton colleagues jumped the gun on this I think:
X. Liang and S. Y. Chou, Nanogap detector inside nano-fuidic channel for fast real-time label-free DNA analysis," Nano Lett., vol. 8, pp. 1472-1476, 2008.
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Our attempt to make an AC-coupledconformal system with low temperature processing for on-chipelectronics.
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1) Electron-beam lithography (EBL) to make nanoelectrodes
2) EBL to make sacrificial PMMA nanochannels
3) parylene-C to make conformal coating of PMMA nanochannels.
4) Sacrificial removal of PMMA
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22 pairs of nanoelectrodes along a 12 mmlong nanochannel
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(A) (B)
NANOCHANNELS
10 nm of SiO2 to make hydrophyllic surface, wet easily (100 nm wide nanochannels)
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NANOCHANNEL
10MICRONS
parylene C autofluorescence precludes single-molecule detection optically.
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External ElectrodesGround
(A)
(B)
p-Si
1) Nanoelectrodes fabricated on 100 nm of SiO2 grown on p-doped Si wafer for ultimate FET operatation.
2) 10 mV RMS drive, no DC bias.
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wafer-electrode coupling
nanochannel
electrolysis channel
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Surprisingly, we understand some aspects of this complex circuit pretty well.
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Bulk buffer
Nanochannel
Longitudinal Impredance (like a nanopore).Monday,11 May, 09
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Fits to bulk water ( just stick two gold wires 12 mm apart into buffer) give good numbers for CDL (10 uF/cm2 ) and conductivity of saline buffer (200 1/ohm-cm).
Fits to nanochannel give conductivity of water in 100 nm nanochannel TOO HIGH by about 4 orders of magnitude!
Big mystery rightnow.
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Transverse impedance measurements between nanoelectrodes more complex because electrodes couple capacitively into p-dope Si wafer substrate of rather low resistivity of about 10 ohm-cm
DryWet
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1) Water barely visible in terms of impedance change compared to dry electrode because of capacitive coupling to substrate.
2) Still get impedance of solvent far too small by about 4 orders of magnitude.
3) DNA detection electronically with high speed HOPELESS with this configuration!
Mothers: don’t let your children try to electronically detect DNA!
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5. Quo vadis?
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1) I think we have to construct nanochannels in front of nanopores in order to wring out the entropy and get control of the molecule pasing by the nanopore.
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!
Figure 0. Diagram of a transverse electrode
configuration, where both electrodes are positioned on the same membrane surface to sense across the pore
aperture, intended to allow new sensing strategies such as measurement of tunneling current through
translocating DNA molecules.
!
Mariija Drndic, U Penn Physics: transverse nanoelectrodes
2) AC-couple transverse nanoelectrodes
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3) On-chip MOSFET amplifiers to locally amplify up expected tiny signals at the pA level at the MHz bandwidths.
Ken Sheppard, EE, Columbia University
Monday,11 May, 09
![Page 47: TOWARDS Electronic Detection of Genomic-length DNA with no ... · e-mail: austin@princeton.edu research as scientists struggle to apply nanotechnology to areas ofbiological interest.One](https://reader034.fdocuments.in/reader034/viewer/2022050222/5f676fd701b841051326d884/html5/thumbnails/47.jpg)
We’ll get there!
Thanks!
Monday,11 May, 09