Department of Chemistry , University of Wisconsin-Madison , Madison , Wisconsin 53706 , United States.
Graduate Program in Biophysics , University of Wisconsin-Madison , Madison , Wisconsin 53706 , United States.
J Am Chem Soc. 2019 Jan 30;141(4):1583-1592. doi: 10.1021/jacs.8b11246. Epub 2019 Jan 15.
The structural principles that govern interactions between l- and d-peptides are not well understood. Among natural proteins, coiled-coil assemblies formed between or among α-helices are the most regular feature of tertiary and quaternary structures. We recently reported the first high-resolution structures for heterochiral coiled-coil dimers, which represent a starting point for understanding associations of l- and d-polypeptides. These structures were an unexpected outcome from crystallization of a racemic peptide corresponding to the transmembrane domain of the influenza A M2 protein (M2-TM). The reported structures raised the possibility that heterochiral coiled-coil dimers prefer an 11-residue (hendecad) sequence repeat, in contrast to the 7-residue (heptad) sequence repeat that is dominant among natural coiled coils. To gain insight on sequence repeat preferences of heterochiral coiled-coils, we have examined three M2-TM variants containing substitutions intended to minimize steric clashes between side chains at the coiled-coil interface. In each of the three new crystal structures, we observed heterochiral coiled-coil associations that closely match a hendecad sequence motif, which strengthens the conclusion that this motif is intrinsic to the pairing of α-helices with opposite handedness. In each case, the presence of a hendecad motif was established by comparing the observed helical frequency to that of an ideal hendecad. This comparison revealed that decreasing the size of the amino acid side chain at positions that project toward the superhelical axis produces tighter packing, as determined by the size of the coiled-coil radius. These results provide a basis for future design of heterochiral coiled-coil pairings.
目前人们对于控制 l- 和 d- 型肽相互作用的结构原理还知之甚少。在天然蛋白质中,α-螺旋之间或之内形成的螺旋束结构是三级和四级结构最常见的特征。我们最近报道了第一个手性杂合螺旋二聚体的高分辨率结构,这为理解 l-和 d-多肽的缔合提供了一个起点。这些结构是流感 A M2 蛋白跨膜结构域(M2-TM)的手性肽的晶体结构的意外结果。所报道的结构提出了这样一种可能性,即手性杂合螺旋二聚体可能优先采用 11 个残基(hendecad)的序列重复,而不是在天然螺旋中占主导地位的 7 个残基(heptad)序列重复。为了深入了解手性杂合螺旋的序列重复偏好性,我们研究了三个 M2-TM 变体,这些变体含有旨在最小化螺旋界面侧链之间空间位阻的取代。在三个新的晶体结构中,我们观察到手性杂合螺旋的缔合与 hendecad 序列基序非常匹配,这加强了这样的结论,即该基序是与相反手性的α-螺旋配对的内在特征。在每种情况下,通过将观察到的螺旋频率与理想 hendecad 的频率进行比较,确定了 hendecad 基序的存在。这种比较表明,减小位于超螺旋轴方向上的氨基酸侧链的大小会产生更紧密的包装,这由螺旋半径的大小决定。这些结果为未来手性杂合螺旋对的设计提供了依据。