Multimodal Measurements of Single-Molecule Dynamics Using FluoRBT

被引:12
|
作者
Ivanov, Ivan E. [1 ,2 ]
Lebel, Paul [2 ,3 ,6 ]
Oberstrass, Florian C. [2 ,7 ]
Starr, Charles H. [2 ,4 ]
Parente, Angelica C. [2 ,4 ]
Ierokomos, Athena [2 ,4 ]
Bryant, Zev [2 ,5 ]
机构
[1] Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Appl Phys, Stanford, CA 94305 USA
[4] Stanford Univ, Program Biophys, Stanford, CA 94305 USA
[5] Stanford Univ, Dept Struct Biol, Stanford, CA 94305 USA
[6] Chan Zuckerberg Biohub, San Francisco, CA USA
[7] Ultima Genom Inc, Fremont, CA USA
基金
美国国家卫生研究院;
关键词
TORQUE MEASUREMENTS; MAGNETIC TWEEZERS; RNA-POLYMERASE; DNA; FLUORESCENCE; FRET; TENSION; FORCE; SPECTROSCOPY; MANIPULATION;
D O I
10.1016/j.bpj.2017.11.017
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Single-molecule methods provide direct measurements of macromolecular dynamics, but are limited by the number of degrees of freedom that can be followed at one time. High-resolution rotor bead tracking (RBT) measures DNA torque, twist, and extension, and can be used to characterize the structural dynamics of DNA and diverse nucleoprotein complexes. Here, we extend RBT to enable simultaneous monitoring of additional degrees of freedom. Fluorescence-RBT (FluoRBT) combines magnetic tweezers, infrared evanescent scattering, and single-molecule FRET imaging, providing real-time multiparameter measurements of complex molecular processes. We demonstrate the capabilities of FluoRBT by conducting simultaneous measurements of extension and FRET during opening and closing of a DNA hairpin under tension, and by observing simultaneous changes in FRET and torque during a transition between right-handed B-form and left-handed Z-form DNA under controlled supercoiling. We discover unanticipated continuous changes in FRET with applied torque, and also show how FluoRBT can facilitate high-resolution FRET measurements of molecular states, by using a mechanical signal as an independent temporal reference for aligning and averaging noisy fluorescence data. By combining mechanical measurements of global DNA deformations with FRET measurements of local conformational changes, FluoRBT will enable multidimensional investigations of systems ranging from DNA structures to large macromolecular machines.
引用
收藏
页码:278 / 282
页数:5
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