High-throughput single-molecule analysis of DNA-protein interactions by tethered particle motion

被引:42
|
作者
Plenat, Thomas [1 ,2 ]
Tardin, Catherine [1 ,2 ]
Rousseau, Philippe [3 ,4 ]
Salome, Laurence [1 ,2 ]
机构
[1] CNRS, Inst Pharmacol & Biol Struct, F-31077 Toulouse, France
[2] Univ Toulouse, UPS, Inst Pharmacol & Biol Struct, F-31077 Toulouse, France
[3] Univ Toulouse, UPS, Lab Microbiol & Genet Mol, F-31000 Toulouse, France
[4] CNRS, Lab Microbiol & Genet Mol, F-31000 Toulouse, France
关键词
GENE; 6; EXONUCLEASE; BACTERIOPHAGE T7; RNA;
D O I
10.1093/nar/gks250
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Tethered particle motion (TPM) monitors the variations in the effective length of a single DNA molecule by tracking the Brownian motion of a bead tethered to a support by the DNA molecule. Providing information about DNA conformations in real time, this technique enables a refined characterization of DNA-protein interactions. To increase the output of this powerful but time-consuming single-molecule assay, we have developed a biochip for the simultaneous acquisition of data from more than 500 single DNA molecules. The controlled positioning of individual DNA molecules is achieved by self-assembly on nanoscale arrays fabricated through a standard microcontact printing method. We demonstrate the capacity of our biochip to study biological processes by applying our method to explore the enzymatic activity of the T7 bacteriophage exonuclease. Our single molecule observations shed new light on its behaviour that had only been examined in bulk assays previously and, more specifically, on its processivity.
引用
收藏
页数:8
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