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单价和二价阳离子对乳糖阻遏物-操纵基因相互作用影响的解读

Interpretation of monovalent and divalent cation effects on the lac repressor-operator interaction.

作者信息

Record M T, deHaseth P L, Lohman T M

出版信息

Biochemistry. 1977 Nov 1;16(22):4791-6. doi: 10.1021/bi00641a005.

Abstract

We have investigated the effects of mixed Na+: Mg2+ ionic solutions on the stability of the nonspecific lac repressor-DNA complex. The effects of Mg2+ are simply interpreted in terms of its role as a competitor (with repressor) for DNA sites. From these studies, the binding constant of the Mg-DNA complex can be determined as a function of the concentration of Na+. We have used this information to interpret the data of Riggs and collaborators (Riggs, A.D., et al. (1970), J. Mol. Biol. 48, 67-83; 53, 401-417) on the ion dependence of the repressor-operator interaction. We find that there are approximately 70% as many ionic interactions in the repressor-operator complex as in the nonspecific complex. Our best estimate is that 8 +/- 1 ion pairs are formed. We calculate that the release of counterions in the formation of the specific complex contributes approximately 40% of the favorable free energy change in the association reaction under in vivo ionic conditions. Implications of these findings for the control of the lac operon and for the molecular relationship between the specific and nonspecific complexes are considered.

摘要

我们研究了混合的Na⁺:Mg²⁺离子溶液对非特异性乳糖阻遏蛋白-DNA复合物稳定性的影响。Mg²⁺的作用可简单解释为它作为(与阻遏蛋白竞争)DNA位点的竞争者。通过这些研究,Mg-DNA复合物的结合常数可确定为Na⁺浓度的函数。我们利用这一信息来解释里格斯及其合作者(里格斯,A.D.等人(1970年),《分子生物学杂志》48卷,67 - 83页;53卷,401 - 417页)关于阻遏蛋白-操纵基因相互作用的离子依赖性数据。我们发现,阻遏蛋白-操纵基因复合物中的离子相互作用数量约为非特异性复合物中的70%。我们的最佳估计是形成了8 ± 1个离子对。我们计算得出,在体内离子条件下,特异性复合物形成过程中反离子的释放约占缔合反应中有利自由能变化的40%。本文考虑了这些发现对乳糖操纵子调控以及特异性和非特异性复合物之间分子关系的影响。

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