Two-component atomic force microscopy recognition imaging of complex samples

被引:7
|
作者
Wang, H.
Bash, R.
Lohr, D. [1 ]
机构
[1] Arizona State Univ, Dept Chem & Biochem, Tempe, AZ 85287 USA
[2] Arizona State Univ, Biodesign Inst, Tempe, AZ 85287 USA
关键词
AFM; SPM; recognition imaging; nucleosomal arrays; hSwi-Snf; chromatin;
D O I
10.1016/j.ab.2006.11.039
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Biological complexes are typically multisubunit in nature and the processes in which they participate often involve protein compositional changes in themselves and/or their target substrates. Being able to identify more than one type of protein in complex samples and to track compositional changes during processes would thus be very useful. Toward this goal, we describe here a single-molecule technique that can simultaneously identify two types of proteins in compositionally complex samples. It is an adaptation of the recently developed atomic force microscopy (AFM) recognition imaging technique but involves the tethering of two different types of antibodies to the AFM tip and sequential blocking with appropriate antigenic peptides to distinguish the recognition from each antibody. The approach is shown to be capable of simultaneously identifying in a single AFM image two specific components, BRGI and beta-actin, of the human Swi-Snf ATP-dependent nucleosome remodeling complex and two types of histones, H2A and H3, in chromatin samples. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:273 / 279
页数:7
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