Interactions of Arg2 in the Mnt N-terminal arm with the central and flanking regions of the mnt operator

被引:7
作者
Berggrun, A [1 ]
Sauer, RT [1 ]
机构
[1] MIT, Dept Biol, Cambridge, MA 02139 USA
关键词
repressor; DNA-binding specificity; ribbon-helix-helix family; protein-DNA interactions;
D O I
10.1006/jmbi.2000.4007
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
Arg2 in the N-terminal arm of the Mnt repressor, plays an important role in determining operator-binding specificity. Ln the complex of the Mnt tetramer with the 21 base-pair mnt operator, there are four potential sites for Arg2 interactions, two in the central region of the operator and two on the outer flanks of the operator. Single-chain variants of the dimeric N-terminal domain of Mnt containing one Arg2 residue and one Lys2 or Met2 residue were constructed and interactions with operator DNA were probed using Fe EDTA affinity cleavage. The results of these orientation studies show that the majority of the energetically significant interactions mediated by Arg2 occur in the central region of the mnt operator. The RK2, RA2, and RM2 mutations reduce the free energy of operator binding by 1.7 kcal/mol, 3.3 kcal/mol, and 4.9 kcal/mol, respectively. Double-mutant thermodynamic cycle analyses using the RA2, RM2, and operator variants also reveal interaction free energies between Arg2 and operator base-pairs 9, 10, 11, 12 and 13, which in aggregate account for most of the Arg2 contribution to operator binding. (C) 2000 Academic Press.
引用
收藏
页码:959 / 973
页数:15
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