Literature DB >> 23077172

Atomic force microscopy - looking at mechanosensors on the cell surface.

Jürgen J Heinisch1, Peter N Lipke, Audrey Beaussart, Sofiane El Kirat Chatel, Vincent Dupres, David Alsteens, Yves F Dufrêne.   

Abstract

Living cells use cell surface proteins, such as mechanosensors, to constantly sense and respond to their environment. However, the way in which these proteins respond to mechanical stimuli and assemble into large complexes remains poorly understood at the molecular level. In the past years, atomic force microscopy (AFM) has revolutionized the way in which biologists analyze cell surface proteins to molecular resolution. In this Commentary, we discuss how the powerful set of advanced AFM techniques (e.g. live-cell imaging and single-molecule manipulation) can be integrated with the modern tools of molecular genetics (i.e. protein design) to study the localization and molecular elasticity of individual mechanosensors on the surface of living cells. Although we emphasize recent studies on cell surface proteins from yeasts, the techniques described are applicable to surface proteins from virtually all organisms, from bacteria to human cells.

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Year:  2012        PMID: 23077172      PMCID: PMC3516434          DOI: 10.1242/jcs.106005

Source DB:  PubMed          Journal:  J Cell Sci        ISSN: 0021-9533            Impact factor:   5.285


  57 in total

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10.  Single-molecule atomic force microscopy reveals clustering of the yeast plasma-membrane sensor Wsc1.

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  16 in total

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Review 6.  LIM proteins in actin cytoskeleton mechanoresponse.

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Review 7.  Techniques for assessing 3-D cell-matrix mechanical interactions in vitro and in vivo.

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8.  Measuring collagen fibril diameter with differential interference contrast microscopy.

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9.  Between Amyloids and Aggregation Lies a Connection with Strength and Adhesion.

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10.  Force Sensitivity in Saccharomyces cerevisiae Flocculins.

Authors:  Cho X J Chan; Sofiane El-Kirat-Chatel; Ivor G Joseph; Desmond N Jackson; Caleen B Ramsook; Yves F Dufrêne; Peter N Lipke
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