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来自人组织培养细胞的纯化DNA松弛酶的特性分析。

Characterization of purified DNA-relaxing enzyme from human tissue culture cells.

作者信息

Keller W

出版信息

Proc Natl Acad Sci U S A. 1975 Jul;72(7):2550-4. doi: 10.1073/pnas.72.7.2550.

Abstract

Superhelical simian virus 40 DNA migrates more rapidly during electrophoresis in agarose gels than covalently closed DNA free of superhelical turns (relaxed DNA). The difference in electrophoretic mobility between superhelical and relaxed DNA was used to monitor the activity of a protein from human tissue culture cells which converts superhelical DNA into relaxed DNA. Purified DNA-relaxing protein removes both negative and positive superhelical turns and acts in a catalytic manner. The relaxation of DNA proceeds in a stepwise fashion and DNA intermediates with decreasing numbers of superhelical turns are seen during the course of the reaction.

摘要

超螺旋猿猴病毒40 DNA在琼脂糖凝胶电泳过程中的迁移速度比没有超螺旋结构的共价闭合DNA(松弛DNA)更快。利用超螺旋DNA和松弛DNA在电泳迁移率上的差异来监测来自人组织培养细胞的一种蛋白质的活性,该蛋白质可将超螺旋DNA转化为松弛DNA。纯化的DNA松弛蛋白可去除负超螺旋和正超螺旋结构,且以催化方式起作用。DNA的松弛以逐步方式进行,在反应过程中可看到超螺旋结构数量减少的DNA中间体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/474e/432806/e1e98c03b972/pnas00050-0086-a.jpg

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