Analysis of ligand-receptor interactions in cells by atomic force microscopy

被引:41
作者
Horton, M [1 ]
Charras, G [1 ]
Lehenkari, P [1 ]
机构
[1] UCL, Dept Med, London WC1E 6JJ, England
来源
JOURNAL OF RECEPTOR AND SIGNAL TRANSDUCTION RESEARCH | 2002年 / 22卷 / 1-4期
关键词
atomic force microscopy; ligand-receptor interaction; binding force; molecular recognition;
D O I
10.1081/RRS-120014594
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
Atomic force microscopy (AFM) increasingly has been used to analyse "receptor" function, either by using purified proteins ("molecular recognition microscopy") or, more recently, in situ in living cells. The latter approach has been enabled by the use of a modified commercial AFM, linked to a confocal microscope, which has allowed adhesion forces between ligands and receptors in cells to be measured and mapped, and downstream cellular responses analysed. We review the application of AFM to cell biology and, in particular, to the study of ligand-receptor interactions and draw examples from our own work and that of others to show the utility of AFM, including for the exploration of cell surface functionalities. We also identify shortcomings of AFM in comparison to "standard" methods, such as receptor auto-radiography or immuno-detection, that are widely applied in cell biology and pharmacological analysis.
引用
收藏
页码:169 / 190
页数:22
相关论文
共 104 条
[1]   Detection of antigen-antibody binding events with the atomic force microscope [J].
Allen, S ;
Chen, XY ;
Davies, J ;
Davies, MC ;
Dawkes, AC ;
Edwards, JC ;
Roberts, CJ ;
Sefton, J ;
Tendler, SJB ;
Williams, PM .
BIOCHEMISTRY, 1997, 36 (24) :7457-7463
[2]  
Ashmore JF, 2001, BIOPHYS J, V80, p306A
[3]   Changes in surface topography in endothelial monolayers with time at confluence: Influence on subcellular shear stress distribution due to flow [J].
Barbee, KA .
BIOCHEMISTRY AND CELL BIOLOGY, 1995, 73 (7-8) :501-505
[4]   Cadherin interaction probed by atomic force microscopy [J].
Baumgartner, W ;
Hinterdorfer, P ;
Ness, W ;
Raab, A ;
Vestweber, D ;
Schindler, H ;
Drenckhahn, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (08) :4005-4010
[5]   Discrete interactions in cell adhesion measured by single-molecule force spectroscopy [J].
Benoit, M ;
Gabriel, D ;
Gerisch, G ;
Gaub, HE .
NATURE CELL BIOLOGY, 2000, 2 (06) :313-317
[6]   ATOMIC FORCE MICROSCOPE [J].
BINNIG, G ;
QUATE, CF ;
GERBER, C .
PHYSICAL REVIEW LETTERS, 1986, 56 (09) :930-933
[7]   Atomic force microscopy study of the adhesion of Saccharomyces cerevisiae [J].
Bowen, WR ;
Lovitt, RW ;
Wright, CJ .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2001, 237 (01) :54-61
[8]   Determination of cellular strains by combined atomic force microscopy and finite element modeling [J].
Charras, GT ;
Horton, MA .
BIOPHYSICAL JOURNAL, 2002, 83 (02) :858-879
[9]   Single cell mechanotransduction and its modulation analyzed by atomic force microscope indentation [J].
Charras, GT ;
Horton, MA .
BIOPHYSICAL JOURNAL, 2002, 82 (06) :2970-2981
[10]   Atomic force microscopy can be used to mechanically stimulate osteoblasts and evaluate cellular strain distributions [J].
Charras, GT ;
Lehenkari, PP ;
Horton, MA .
ULTRAMICROSCOPY, 2001, 86 (1-2) :85-95