Structure and Dynamics of the Kinesin-Microtubule Interaction Revealed by Fluorescence Polarization Microscopy

被引:5
|
作者
Sosa, Hernando [1 ]
Asenjo, Ana B. [1 ]
Peterman, Erwin J. G. [2 ,3 ]
机构
[1] Albert Einstein Coll Med, Dept Physiol & Biophys, Bronx, NY 10461 USA
[2] Vrije Univ Amsterdam, Dept Phys & Astron, NL-1081 HV Amsterdam, Netherlands
[3] Vrije Univ Amsterdam, Ctr Laser, NL-1081 HV Amsterdam, Netherlands
来源
MICROTUBULES, IN VITRO: MICROTUBULES, IN VITRO | 2010年 / 95卷
关键词
LIGHT-CHAIN; MUSCLE-FIBERS; MYOSIN-V; SINGLE; ORIENTATION; FLUOROPHORE; PROTEIN; MOTORS; LOCALIZATION; SPECTROSCOPY;
D O I
10.1016/S0091-679X(10)95025-5
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Fluorescence polarization microscopy (FPM) is the analysis of the polarization of light in a fluorescent microscope in order to determine the angular orientation and rotational mobility of fluorescent molecules. Key advantages of FPM, relative to other structural analysis techniques, are that it allows the detection of conformational changes of fluorescently labeled macromolecules in real time in physiological conditions and at the single-molecule level. In this chapter we describe in detail the FPM experimental set-up and analysis methods we have used to investigate structural intermediates of the motor protein kinesin-1 associated with its walking mechanism along microtubules. We also briefly describe additional FPM methods that have been used to investigate other macromolecular complexes.
引用
收藏
页码:505 / 519
页数:15
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