Visible/near-infrared subdiffraction imaging reveals the stochastic nature of DNA walkers

Super-resolution imaging reveals the stochastic behavior of DNA walkers. DNA walkers are designed with the structural specificity and functional diversity of oligonucleotides to actively convert chemical energy into mechanical translocation. Compared to natural protein motors, DNA walkers’ small translocation distance (mostly <100 nm) and slow reaction rate (<0.1 nm s−1) make single-molecule characterization of their kinetics elusive. An important indication of single-walker kinetics is the rate-limiting reactions that a particular walker design bears. We introduce an integrated super-resolved fluorescence microscopy approach that is capable of long-term imaging to investigate the stochastic behavior of DNA walkers. Subdiffraction tracking and imaging in the visible and second near-infrared spectra resolve walker structure and reaction rates. The distributions of walker kinetics are analyzed using a stochastic model to reveal reaction randomness and the rate-limiting biochemical reaction steps.

[1]  Jing Pan,et al.  DNA Walker‐Regulated Cancer Cell Growth Inhibition , 2016, Chembiochem : a European journal of chemical biology.

[2]  Xiaogang Peng,et al.  Experimental Determination of the Extinction Coefficient of CdTe, CdSe, and CdS Nanocrystals , 2003 .

[3]  Taekjip Ha,et al.  An Improved Surface Passivation Method for Single-Molecule Studies , 2014, Nature Methods.

[4]  V. C. Moore,et al.  Band Gap Fluorescence from Individual Single-Walled Carbon Nanotubes , 2002, Science.

[5]  R. Astumian Thermodynamics and kinetics of a Brownian motor. , 1997, Science.

[6]  M. Zheng,et al.  Molecular-crowding-induced clustering of DNA-wrapped carbon nanotubes for facile length fractionation. , 2011, ACS nano.

[7]  Hao Yan,et al.  Robust DNA-functionalized core/shell quantum dots with fluorescent emission spanning from UV-vis to near-IR and compatible with DNA-directed self-assembly. , 2012, Journal of the American Chemical Society.

[8]  M. Strano,et al.  Understanding oligonucleotide-templated nanocrystals: growth mechanisms and surface properties. , 2012, ACS nano.

[9]  Ming Zheng,et al.  DNA sequence motifs for structure-specific recognition and separation of carbon nanotubes , 2009, Nature.

[10]  K. Jacobson,et al.  Single-particle tracking: applications to membrane dynamics. , 1997, Annual review of biophysics and biomolecular structure.

[11]  G. F. Joyce,et al.  A general purpose RNA-cleaving DNA enzyme. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[12]  S. Hess,et al.  Precisely and accurately localizing single emitters in fluorescence microscopy , 2014, Nature Methods.

[13]  Paul R Selvin,et al.  Fluorescence imaging with one nanometer accuracy: application to molecular motors. , 2005, Accounts of chemical research.

[14]  Jing Pan,et al.  Recent progress on DNA based walkers. , 2015, Current opinion in biotechnology.

[15]  Haorong Chen,et al.  Multiplexed optical detection of plasma porphyrins using DNA aptamer-functionalized carbon nanotubes. , 2013, Analytical chemistry.

[16]  Harry M. T. Choi,et al.  Programming biomolecular self-assembly pathways , 2008, Nature.

[17]  Erik Winfree,et al.  Molecular robots guided by prescriptive landscapes , 2010, Nature.

[18]  Miran Liber,et al.  Developing DNA nanotechnology using single-molecule fluorescence. , 2014, Accounts of chemical research.

[19]  Yan Liu,et al.  Aqueous synthesis of glutathione-capped CdTe/CdS/ZnS and CdTe/CdSe/ZnS core/shell/shell nanocrystal heterostructures. , 2012, Langmuir : the ACS journal of surfaces and colloids.

[20]  David A Leigh,et al.  Walking molecules. , 2011, Chemical Society reviews.

[21]  R. Weisman,et al.  Subdiffraction far-field imaging of luminescent single-walled carbon nanotubes. , 2008, Nano letters.

[22]  Yang Liu,et al.  High-speed DNA-based rolling motors powered by RNase H , 2015, Nature nanotechnology.

[23]  A. Turberfield,et al.  Direct observation of stepwise movement of a synthetic molecular transporter. , 2011, Nature nanotechnology.

[24]  K. Svoboda,et al.  Fluctuation analysis of motor protein movement and single enzyme kinetics. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[25]  Henry Pinkard,et al.  Advanced methods of microscope control using μManager software. , 2014, Journal of biological methods.

[26]  M. Schnitzer,et al.  Statistical kinetics of processive enzymes. , 1995, Cold Spring Harbor symposia on quantitative biology.

[27]  Characterization of non-8-17 sequences uncovers structurally diverse RNA-cleaving deoxyribozymes. , 2011, Molecular bioSystems.

[28]  M. Zheng,et al.  DNA-assisted dispersion and separation of carbon nanotubes , 2003, Nature materials.

[29]  Antoine M. van Oijen,et al.  Ever-fluctuating single enzyme molecules: Michaelis-Menten equation revisited , 2006, Nature chemical biology.

[30]  Ruojie Sha,et al.  A Bipedal DNA Brownian Motor with Coordinated Legs , 2009, Science.

[31]  Juan Cheng,et al.  From bistate molecular switches to self-directed track-walking nanomotors. , 2014, ACS nano.

[32]  Daphne Weihs,et al.  Particle tracking in living cells: a review of the mean square displacement method and beyond , 2013, Rheologica Acta.

[33]  Antoine M. van Oijen,et al.  Analysis of kinetic intermediates in single-particle dwell-time distributions. , 2010, Biophysical journal.

[34]  Michael Unser,et al.  A pyramid approach to subpixel registration based on intensity , 1998, IEEE Trans. Image Process..

[35]  Euan R Kay,et al.  Rise of the Molecular Machines , 2015, Angewandte Chemie.

[36]  Shana O Kelley,et al.  One-step DNA-programmed growth of luminescent and biofunctionalized nanocrystals. , 2009, Nature nanotechnology.

[37]  A. Caspi,et al.  Enhanced diffusion in active intracellular transport. , 2000, Physical review letters.

[38]  David A Leigh,et al.  A synthetic small molecule that can walk down a track. , 2010, Nature chemistry.

[39]  Paul S Weiss,et al.  Controlling Motion at the Nanoscale: Rise of the Molecular Machines. , 2015, ACS nano.

[40]  Friedrich C. Simmel,et al.  Diffusive transport of molecular cargo tethered to a DNA origami platform. , 2015, Nano letters.

[41]  A. Jagota,et al.  Molecular-basis of single-walled carbon nanotube recognition by single-stranded DNA. , 2012, Nano letters.

[42]  Jing Pan,et al.  A synthetic DNA motor that transports nanoparticles along carbon nanotubes. , 2014, Nature nanotechnology.

[43]  G. F. Joyce,et al.  Mechanism and utility of an RNA-cleaving DNA enzyme. , 1998, Biochemistry.

[44]  Jing Pan,et al.  Design Principles of DNA Enzyme-Based Walkers: Translocation Kinetics and Photoregulation. , 2015, Journal of the American Chemical Society.

[45]  Akihiro Kusumi,et al.  Detection of non-Brownian diffusion in the cell membrane in single molecule tracking. , 2005, Biophysical journal.

[46]  Ming Zheng,et al.  Understanding the Nature of the DNA-Assisted Separation of Single-Walled Carbon Nanotubes Using Fluorescence and Raman Spectroscopy , 2004 .

[47]  A. Turberfield,et al.  Programmable energy landscapes for kinetic control of DNA strand displacement , 2014, Nature Communications.