Single-Molecule Reaction Chemistry in Patterned Nanowells

被引:45
作者
Bouilly, Delphine [1 ]
Hon, Jason [1 ]
Daly, Nathan S. [1 ]
Trocchia, Scott [2 ]
Vernick, Sefi [2 ]
Yu, Jaeeun [1 ]
Warren, Steven [2 ]
Wu, Ying [1 ]
Gonzalez, Ruben L., Jr. [1 ]
Shepard, Kenneth L. [2 ]
Nuckolls, Colin [1 ]
机构
[1] Columbia Univ, Dept Chem, 3000 Broadway, New York, NY 10027 USA
[2] Columbia Univ, Dept Elect Engn, 500 W 120th St, New York, NY 10027 USA
基金
美国国家科学基金会; 加拿大自然科学与工程研究理事会; 美国国家卫生研究院;
关键词
Single-molecule; electrical conductance; electronic devices; sensors; biofunctionalization; carbon nanotubes; WALLED CARBON NANOTUBES; G-QUADRUPLEX; CHEMICAL FUNCTIONALIZATION; DNA; KINETICS; SPECTROSCOPY; PATHWAYS; DYNAMICS; SEQUENCE;
D O I
10.1021/acs.nanolett.6b02149
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new approach to synthetic chemistry is performed in ultraminiaturized, nanofabricated reaction chambers. Using lithographically defined nanowells, we achieve single-point covalent chemistry on hundreds of individual carbon nanotube transistors, providing robust statistics and unprecedented spatial resolution in adduct position. Each device acts as a sensor to detect, in real-time and through quantized changes in conductance, single-point functionalization of the nanotube as well as consecutive chemical reactions, molecular interactions, and molecular conformational changes occurring on the resulting single-molecule probe. In particular, we use a set of sequential bioconjugation reactions to tether a single-strand of DNA to the device and record its repeated, reversible folding into a G-quadruplex structure. The stable covalent tether allows us to measure the same molecule in different solutions, revealing the characteristic increased stability of the G-quadruplex structure in the presence of potassium ions (K+) versus sodium ions (Na+). Nanowell-confined reaction chemistry on carbon nanotube devices offers a versatile method to isolate and monitor individual molecules during successive chemical reactions over an extended period of time.
引用
收藏
页码:4679 / 4685
页数:7
相关论文
共 43 条
[1]   Human telomeric sequence forms a hybrid-type intramolecular G-quadruplex structure with mixed parallel/antiparallel strands in potassium solution [J].
Ambrus, Attila ;
Chen, Ding ;
Dai, Jixun ;
Bialis, Tiffanie ;
Jones, Roger A. ;
Yang, Danzhou .
NUCLEIC ACIDS RESEARCH, 2006, 34 (09) :2723-2735
[2]  
Ashraf M.K., 2009, Phys. Rev. B - Condens. Matter Mater. Phys, V79, P1
[3]   Covalent chemistry of single-wall carbon nanotubes [J].
Bahr, JL ;
Tour, JM .
JOURNAL OF MATERIALS CHEMISTRY, 2002, 12 (07) :1952-1958
[4]   Graft-Induced Midgap States in Functionalized Carbon Nanotubes [J].
Bouilly, Delphine ;
Janssen, Jonathan Laflamme ;
Cabana, Janie ;
Cote, Michel ;
Martel, Richard .
ACS NANO, 2015, 9 (03) :2626-2634
[5]   Unaltered electrical conductance in single-walled carbon nanotubes functionalized with divalent adducts [J].
Bouilly, Delphine ;
Cabana, Janie ;
Martel, Richard .
APPLIED PHYSICS LETTERS, 2012, 101 (05)
[6]  
Bronson J. E., 2009, ARXIV09073156QBIOQM
[7]   Automated Maximum Likelihood Separation of Signal from Baseline in Noisy Quantal Data [J].
Bruno, William J. ;
Ullah, Ghanim ;
Mak, Don-On Daniel ;
Pearson, John E. .
BIOPHYSICAL JOURNAL, 2013, 105 (01) :68-79
[8]   Quadruplex DNA: sequence, topology and structure [J].
Burge, Sarah ;
Parkinson, Gary N. ;
Hazel, Pascale ;
Todd, Alan K. ;
Neidle, Stephen .
NUCLEIC ACIDS RESEARCH, 2006, 34 (19) :5402-5415
[9]   Thermal Chemistry of Methylene- and Phenyl-Functionalized Carbon Nanotubes [J].
Cabana, Janie ;
Lavoie, Stephane ;
Martel, Richard .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2010, 132 (04) :1389-1394
[10]   Single-Molecule Lysozyme Dynamics Monitored by an Electronic Circuit [J].
Choi, Yongki ;
Moody, Issa S. ;
Sims, Patrick C. ;
Hunt, Steven R. ;
Corso, Brad L. ;
Perez, Israel ;
Weiss, Gregory A. ;
Collins, Philip G. .
SCIENCE, 2012, 335 (6066) :319-324