Capturing the nanoscale complexity of cellular membranes in supported lipid bilayers

被引:21
作者
Kam, Lance C. [1 ]
机构
[1] Columbia Univ, Dept Biomed Engn, New York, NY 10027 USA
关键词
Lipid bilayer; Hop diffusion; Microdomain; Nanotechnology; FLUORESCENCE CORRELATION SPECTROSCOPY; SINGLE-MOLECULE TRACKING; PLASMA-MEMBRANE; LATERAL MOBILITY; PHOTOBLEACHING RECOVERY; ANOMALOUS SUBDIFFUSION; IMMUNOLOGICAL SYNAPSE; COMPOSITION ARRAYS; LIVE CELLS; T-CELLS;
D O I
10.1016/j.jsb.2009.05.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The lateral mobility of cell membranes plays an important role in cell signaling, governing the rate at which embedded proteins can interact with other biomolecules. The past two decades have seen a dramatic transformation in understanding of this environment, as the mechanisms and potential implications of nanoscale structure of these systems has become accessible to theoretical and experimental investigation. In particular, emerging micro-and nano-scale fabrication techniques have made possible the direct manipulation of model membranes at the scales relevant to these biological processes. This review focuses on recent advances in nanopatterning of supported lipid bilayers, capturing the impact of membrane nanostructure on molecular diffusion and providing a powerful platform for further investigation of the role of this spatial complexity on cell signaling. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:3 / 10
页数:8
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