Tramontano A, Chothia C, Lesk A M
European Molecular Biology Laboratory, Heidelberg, F.R.G.
J Mol Biol. 1990 Sep 5;215(1):175-82. doi: 10.1016/S0022-2836(05)80102-0.
Analysis of the immunoglobulins of known structure reveals systematic differences in the position and main-chain conformation of the second hypervariable region of the VH domain (H2). We show that the major determinant of the position of H2 is the size of the residue at site 71, a site that is in the conserved framework of the VH domain. It is likely that for about two thirds of the known VH sequences the size of the residue at this site is also a major determinant of the conformation of H2. This effect can override the predisposition of the sequence, as in the case of the H2 loop of J539, which is an exception to the rules relating sequence and conformation of short hairpin loops. Understanding the relationship between the residue at position 71 and the position and conformation of H2 has applications to the prediction and engineering of antigen-binding sites of immunoglobulins.
对已知结构的免疫球蛋白进行分析后发现,VH结构域(H2)的第二个高变区在位置和主链构象上存在系统性差异。我们发现,H2位置的主要决定因素是第71位残基的大小,该位点位于VH结构域的保守框架内。对于大约三分之二的已知VH序列而言,该位点残基的大小可能也是H2构象的主要决定因素。这种效应可以超越序列的倾向性,例如J539的H2环就是一个例子,它是与短发夹环的序列和构象相关规则的一个例外。了解第71位残基与H2的位置和构象之间的关系,对于免疫球蛋白抗原结合位点的预测和工程设计具有应用价值。