Gold rotor bead tracking for high-speed measurements of DNA twist, torque and extension

被引:68
作者
Lebel, Paul [1 ,2 ]
Basu, Aakash [1 ,2 ]
Oberstrass, Florian C. [2 ]
Tretter, Elsa M. [3 ]
Bryant, Zev [2 ,4 ]
机构
[1] Stanford Univ, Dept Appl Phys, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
[3] Univ Calif Berkeley, Dept Cell & Mol Biol, Berkeley, CA 94720 USA
[4] Stanford Univ, Med Ctr, Dept Biol Struct, Stanford, CA 94305 USA
基金
瑞士国家科学基金会; 美国国家卫生研究院; 加拿大自然科学与工程研究理事会;
关键词
ESCHERICHIA-COLI DNA; SINGLE-MOLECULE; MAGNETIC TWEEZERS; RNA-POLYMERASE; STRUCTURAL TRANSITIONS; MEASUREMENTS REVEAL; OPTICAL TWEEZERS; SUPERCOILED DNA; RESOLUTION; GYRASE;
D O I
10.1038/nmeth.2854
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Single-molecule measurements of DNA twist and extension have been used to reveal physical properties of the double helix and to characterize structural dynamics and mechanochemistry in nucleoprotein complexes. However, the spatiotemporal resolution of twist measurements has been limited by the use of angular probes with high rotational drag, which prevents detection of short-lived intermediates or small angular steps. We introduce gold rotor bead tracking (AuRBT), which yields >100x improvement in time resolution over previous techniques. AuRBT employs gold nanoparticles as bright low-drag rotational and extensional probes, which are monitored by instrumentation that combines magnetic tweezers with objective-side evanescent darkfield microscopy. Our analysis of high-speed structural dynamics of DNA gyrase using AuRBT revealed an unanticipated transient intermediate. AuRBT also enables direct measurements of DNA torque with >50x shorter integration times than previous techniques; we demonstrated high-resolution torque spectroscopy by mapping the conformational landscape of a Z-forming DNA sequence.
引用
收藏
页码:456 / +
页数:9
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