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一个埋藏的极性相互作用可以指导卷曲螺旋中螺旋的相对取向。

A buried polar interaction can direct the relative orientation of helices in a coiled coil.

作者信息

Oakley M G, Kim P S

机构信息

Howard Hughes Medical Institute, Whitehead Institute for Biomedical Research, Department of Biology, Cambridge, Massachusetts 02142, USA.

出版信息

Biochemistry. 1998 Sep 8;37(36):12603-10. doi: 10.1021/bi981269m.

Abstract

Coiled coils consist of bundles of two or more alpha-helices that are aligned in a parallel or an antiparallel relative orientation. The designed peptides, Acid-p1 and Base-p1, associate in solution to form a parallel, heterodimeric two-stranded coiled coil [O'Shea, E. K., Lumb, K. J., and Kim, P. S. (1993) Curr. Biol. 3, 658]. The buried interface of this complex is formed by hydrophobic Leu residues, with the exception of an Asn residue from each strand that is positioned to engage in a buried polar interaction. Substitution of these buried Asn residues by Leu residues results in a loss of structural uniqueness, as evidenced by a lack of a particular helix orientation in the Acid-Base coiled-coil complex [Lumb, K. J., and Kim, P. S. (1995) Biochemistry 34, 8642]. Here, we alter the positions of the Asn residues in the Acid and Base peptides such that a buried polar interaction is only expected to occur when the helices are in an antiparallel orientation. The resulting peptides, Acid-a1 and Base-a1, associate to form a helical heterodimer, as shown by circular dichroism (CD) and equilibrium sedimentation centrifugation. The helix orientation preference has been measured using covalently linked, disulfide-containing heterodimers in which the constituent peptides are constrained to interact in either a parallel or an antiparallel orientation. Although both the parallel and antiparallel heterodimers form stable, helical structures, the antiparallel heterodimer is the predominant species at equilibrium when the heterodimers are allowed to undergo thiol-disulfide exchange. In addition, the antiparallel heterodimer is more stable to chemical denaturation than the parallel counterpart by approximately 2.3 kcal/mol. These results demonstrate that a single buried polar interaction in the interface between the helices of a coiled coil is sufficient to determine the relative orientation of its constituent helices.

摘要

卷曲螺旋由两个或更多α-螺旋束组成,这些螺旋以平行或反平行的相对取向排列。设计的肽Acid-p1和Base-p1在溶液中缔合形成平行的异源二聚体双链卷曲螺旋[奥谢,E.K.,伦布,K.J.,和金,P.S.(1993年)《当代生物学》3,658]。该复合物的埋藏界面由疏水亮氨酸残基形成,每条链上有一个天冬酰胺残基除外,该天冬酰胺残基的位置可参与埋藏的极性相互作用。用亮氨酸残基取代这些埋藏的天冬酰胺残基会导致结构独特性丧失,这在Acid-Base卷曲螺旋复合物中缺乏特定的螺旋取向得到证明[伦布,K.J.,和金,P.S.(1995年)《生物化学》34,8642]。在这里,我们改变了Acid和Base肽中天冬酰胺残基的位置,使得只有当螺旋处于反平行取向时才预期会发生埋藏的极性相互作用。所得的肽Acid-a1和Base-a1缔合形成螺旋异源二聚体,如圆二色性(CD)和平衡沉降离心所示。使用共价连接的含二硫键的异源二聚体测量了螺旋取向偏好,其中组成肽被限制以平行或反平行取向相互作用。虽然平行和反平行异源二聚体都形成稳定的螺旋结构,但当允许异源二聚体进行硫醇-二硫键交换时,反平行异源二聚体在平衡时是主要物种。此外,反平行异源二聚体比平行异源二聚体对化学变性更稳定,约为2.3千卡/摩尔。这些结果表明,卷曲螺旋螺旋之间界面中的单个埋藏极性相互作用足以确定其组成螺旋的相对取向。

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