PURIFICATION AND CHARACTERIZATION OF THE TNSB PROTEIN OF TN7 - A TRANSPOSITION PROTEIN THAT BINDS TO THE ENDS OF TN7

被引:15
作者
TANG, Y
LICHTENSTEIN, C
COTTERILL, S
机构
[1] IMPERIAL COLL SCI TECHNOL & MED,DEPT BIOCHEM,EXHIBIT RD,LONDON SW7 2AZ,ENGLAND
[2] IMPERIAL COLL SCI TECHNOL & MED,CTR BIOTECHNOL,LONDON SW7 2AZ,ENGLAND
基金
英国医学研究理事会;
关键词
D O I
10.1093/nar/19.12.3395
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
Tn7, a large bacterial transposon encodes 5 proteins required for its transposition. We report a rapid and easy purification of one of these proteins, TnsB, from an overexpression strain. This protein was shown to bind to the ends of Tn7, in a bandshift assay, in two distinct stages as a function of protein concentration. DNasel footprinting at each end of Tn7 showed that the TnsB recognition sequence, a set of 22 bp repeats, plus Tn7 termini are protected. Binding of TnsB appeared cooperative but was only observed above a threshold concentration of protein. ATP and Mg2+ had no effect on the pattern of protection, nor did addition of other Tn7-encoded proteins. Hydroxyl radical footprinting, performed at the right end, showed that TnsB binds preferentially to one side of the DNA helix.
引用
收藏
页码:3395 / 3402
页数:8
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