Analytical ultracentrifugation and agarose gel electrophoresis as tools for studying chromatin folding in solution

被引:22
作者
Hansen, JC
Kreider, JI
Demeler, B
Fletcher, TM
机构
[1] Department of Biochemistry, Univ. of Texas Hlth. Sci. Ctr. at S., San Antonio, TX 78284-7760
来源
METHODS-A COMPANION TO METHODS IN ENZYMOLOGY | 1997年 / 12卷 / 01期
关键词
D O I
10.1006/meth.1997.0448
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Analytical ultracentrifugation and agarose gel electrophoresis each can be used to accurately quantify changes in structure that accompany chromatin folding in solution. Analytical ultracentrifugation directly measures the extent of compaction of each species present in a chromatin sample under a wide range of solution conditions. Agarose gel electrophoresis yields information about changes in the average surface charge density, size and/or shape, and conformational flexibility during chromatin folding. When used together, these methodologies are particularly powerful. Protocols for the characterization of chromatin folding by analytical ultracentrifugation and agarose gel electrophoresis are described. Discussion focuses on analysis and interpretation of experimental chromatin folding data. (C) 1997 Academic Press.
引用
收藏
页码:62 / 72
页数:11
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