FORCE FLUORESCENCE SPECTROSCOPY AT THE SINGLE-MOLECULE LEVEL

被引:23
作者
Zhou, Ruobo [1 ,2 ]
Schlierf, Michael [1 ,2 ]
Ha, Taekjip [1 ,2 ,3 ]
机构
[1] Univ Illinois, Dept Phys, Urbana, IL 61801 USA
[2] Univ Illinois, Ctr Phys Living Cells, Urbana, IL 61801 USA
[3] Howard Hughes Med Inst, Urbana, IL USA
来源
METHODS IN ENZYMOLOGY, VOL 475: SINGLE MOLECULE TOOLS, PT B: SUPER-RESOLUTION, PARTICLE TRACKING, MULTIPARAMETER, AND FORCE BASED METHODS | 2010年 / 475卷
关键词
PROTEIN; LANDSCAPE; GUIDE; FRET; DNA;
D O I
10.1016/S0076-6879(10)75016-3
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
During the past decade, various powerful single-molecule techniques have evolved and helped to address important questions in life sciences. Yet these techniques would be even more powerful if they would be combined, that is, single-molecule manipulation with an orthogonal single-molecule observation. Here, we present a recently developed approach to combine single-molecule optical tweezers with single-molecule fluorescence spectroscopy. Optical tweezers are used to manipulate and observe mechanical properties on the nanometer scale and piconewton force range. However, once the force range is in the low piconewton range or less, the spatial resolution of optical tweezers decreases significantly. In combination with fluorescence spectroscopy, like Forster resonance energy transfer (FRET), we are able to observe nanometer fluctuations and internal conformational changes in a low-force regime. The possibility to place fluorescent labels at nearly any desired position and a sophisticated design of the experiment increases the amount of information that can be extracted in contrast to pure mechanical or fluorescence experiments.
引用
收藏
页码:405 / 426
页数:22
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