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通过改变表面静电来改变二聚化特异性。

Altering dimerization specificity by changes in surface electrostatics.

作者信息

Nohaile M J, Hendsch Z S, Tidor B, Sauer R T

机构信息

Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

出版信息

Proc Natl Acad Sci U S A. 2001 Mar 13;98(6):3109-14. doi: 10.1073/pnas.051624498. Epub 2001 Feb 27.

Abstract

Arc repressor forms a homodimer in which the subunits intertwine to create a single globular domain. To obtain Arc sequences that fold preferentially as heterodimers, variants with surface patches of excess positive or negative charge were designed. Several but not all oppositely charged sequence pairs showed preferential heterodimer formation. In the most successful design pair, alpha helix B of one subunit contained glutamic acids at positions 43, 46, 47, 48, and 50, whereas the other subunit contained lysines or arginines at these positions. A continuum electrostatic model captures many features of the experimental results and suggests that the most successful designs include elements of both positive and negative design.

摘要

Arc阻遏蛋白形成一个同型二聚体,其中亚基相互缠绕形成一个单一的球状结构域。为了获得优先折叠为异源二聚体的Arc序列,设计了具有过量正电荷或负电荷表面斑块的变体。几个但并非所有带相反电荷的序列对都显示出优先形成异源二聚体。在最成功的设计对中,一个亚基的α螺旋B在43、46、47、48和50位含有谷氨酸,而另一个亚基在这些位置含有赖氨酸或精氨酸。一个连续静电模型捕捉了实验结果的许多特征,并表明最成功的设计包括正设计和负设计的元素。

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