Methods to measure the lateral diffusion of membrane lipids and proteins

被引:119
作者
Chen, Yun
Lagerholm, B. Christoffer
Yang, Bing
Jacobson, Ken [1 ]
机构
[1] Univ N Carolina, Dept Cell & Dev Biol, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
[3] Univ So Denmark, MEMPHYS, DK-5230 Odense M, Denmark
关键词
FRAP; fluorescence correlation spectroscopy (FCS); single particle tracking (SPT); light microscope; laser; fluorescent probes;
D O I
10.1016/j.ymeth.2006.05.008
中图分类号
Q5 [生物化学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
In this chapter, we discuss methods to measure lateral mobility of membrane lipids and proteins using techniques based on the light microscope. These methods typically sample lateral mobility in very small, micron-sized regions of the membrane so that they can be used to measure diffusion in regions of single cells. The methods are based on fluorescence from the molecules of interest or from light scattered from particles attached to single or small groups of membrane lipids or proteins. Fluorescence recovery after photobleaching (FRAP), fluorescence correlation spectroscopy (FCS) and Single particle tracking (SPT) are presented in that order. FRAP and FCS methodologies are described for a dedicated wide field microscope although many confocal microscopes now have software permitting these measurement to be made; nevertheless, the principles of the measurement are the same for a wide field or confocal microscope. SPT can be applied to trace the movements of single fluorescent molecules in membranes but this aspect will not be treated in detail. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:147 / 153
页数:7
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