A framework is presented for understanding the common character of proteins. Proteins are linear chain molecules. However, the simple model of a polymer viewed as spheres tethered together does not account for many of the observed characteristics of protein structures. The authors show here that proteins may be regarded as tubes of nonzero thickness. This approach allows one to bridge the conventional compact polymer phase with a novel phase employed by Nature to house biomolecular structures. The continuum description of a tube (or a sheet) of arbitrary thickness entails using appropriately chosen many-body interactions rather than two-body interactions. The authors suggest that the structures of folded proteins are selected based on geometrical considerations and are poised at the edge of compaction, thus accounting for their versatility and flexibility. This approach also offers an explanation for why helices and sheets are the building blocks of protein structures.
翻译:蛋白质是一个框架,用于了解蛋白质的共性。蛋白质是线性链分子。然而,作为球体捆绑在一起的聚合物的简单模型并不反映蛋白质结构的许多观察到的特性。作者在这里表明,蛋白质可以被视为非零厚的管子。这种方法可以将常规的紧凑聚合物阶段与自然用于容纳生物分子结构的新阶段相连接。任意厚度管(或薄片)的连续描述需要使用适当选择的多体相互作用,而不是两体相互作用。作者认为,折叠蛋白质的结构是根据几何因素选择的,并处于紧凑的边缘,从而说明其多功能性和灵活性。这种方法还解释了为何 helics和薄片是蛋白质结构的构件。