Single-molecule fluorescence microscopy of native macromolecular complexes

被引:33
作者
Aggarwal, Vasudha [1 ]
Ha, Taekjip [1 ,2 ,3 ,4 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Biophys & Biophys Chem, Baltimore, MD 21218 USA
[2] Johns Hopkins Univ, Dept Biophys, Baltimore, MD 21218 USA
[3] Johns Hopkins Univ, Dept Biomed Engn, Baltimore, MD 21218 USA
[4] Howard Hughes Med Inst, Baltimore, MD USA
关键词
RNA BINDING-PROTEINS; PULL-DOWN; DNA-REPLICATION; DYNAMICS; STOICHIOMETRY; NUCLEOSOMES; ASSOCIATION; TELOMERASE; CHANNELS; RECEPTOR;
D O I
10.1016/j.sbi.2016.09.006
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
Macromolecular complexes consisting of proteins, lipids, and/or nucleic acids are ubiquitous in biological processes. Their composition, stoichiometry, order of assembly, and conformations can be heterogeneous or can change dynamically, making single-molecule studies best suited to measure these properties accurately. Recent single-molecule pull-down and other related approaches have combined the principles of conventional co-immunoprecipitation assay with single-molecule fluorescence microscopy to probe native macromolecular complexes. In this review, we present the advances in single-molecule pull-down methods and biological systems that have been investigated in such semi vivo manner.
引用
收藏
页码:225 / 232
页数:8
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