Minami Shintaro, Chikenji George, Ota Motonori
Department of Complex Systems Science, Graduate School of Informatics, Nagoya University, Nagoya, 464-8601, Japan.
Department of Computational Science and Engineering, Graduate School of Engineering, Nagoya University, Nagoya, 464-8601, Japan.
Protein Sci. 2017 Nov;26(11):2257-2267. doi: 10.1002/pro.3285. Epub 2017 Sep 19.
In protein structures, the fold is described according to the spatial arrangement of secondary structure elements (SSEs: α-helices and β-strands) and their connectivity. The connectivity or the pattern of links among SSEs is one of the most important factors for understanding the variety of protein folds. In this study, we introduced the connectivity strings that encode the connectivities by using the types, positions, and connections of SSEs, and computationally enumerated all the connectivities of two-layer αβ sandwiches. The calculated connectivities were compared with those in natural proteins determined using MICAN, a nonsequential structure comparison method. For 2α-4β, among 23,000 of all connectivities, only 48 were free from irregular connectivities such as loop crossing. Of these, only 20 were found in natural proteins and the superfamilies were biased toward certain types of connectivities. A similar disproportional distribution was confirmed for most of other spatial arrangements of SSEs in the two-layer αβ sandwiches. We found two connectivity rules that explain the bias well: the abundances of interlayer connecting loops that bridge SSEs in the distinct layers; and nonlocal β-strand pairs, two spatially adjacent β-strands located at discontinuous positions in the amino acid sequence. A two-dimensional plot of these two properties indicated that the two connectivity rules are not independent, which may be interpreted as a rule for the cooperativity of proteins.
在蛋白质结构中,折叠是根据二级结构元件(SSEs:α螺旋和β链)的空间排列及其连接性来描述的。SSEs之间的连接性或连接模式是理解蛋白质折叠多样性的最重要因素之一。在本研究中,我们引入了连接串,通过使用SSEs的类型、位置和连接来编码连接性,并通过计算枚举了两层αβ三明治的所有连接性。将计算得到的连接性与使用非顺序结构比较方法MICAN确定的天然蛋白质中的连接性进行了比较。对于2α-4β,在所有23000种连接性中,只有48种没有诸如环交叉等不规则连接。其中,只有20种在天然蛋白质中被发现,并且超家族偏向于某些类型的连接性。对于两层αβ三明治中SSEs的大多数其他空间排列,也证实了类似的不均衡分布。我们发现了两条很好地解释这种偏向性的连接规则:连接不同层中SSEs的层间连接环的丰度;以及非局部β链对,即位于氨基酸序列中不连续位置的两个空间相邻的β链。这两个属性的二维图表明这两条连接规则不是独立的,这可以解释为蛋白质协同作用的规则。