Department of Biochemistry, University of Bristol, Bristol, UK.
Vox Sang. 2011 Jan;100(1):129-39. doi: 10.1111/j.1423-0410.2010.01424.x.
The red cell surface membranes contain a large variety of proteins, many of which express blood group activity as a result of variation in their oligosaccharide or amino acid sequences. To understand the nature of the blood group epitopes, the functions of the proteins that express them and their relationship to each other, computer modelling has been employed to provide predictions of their structures. Modelling is an excellent method of first resort when experimental structural data for the protein of interest are absent or incomplete. The model can then be used to explain previous experimental data and to direct future experiments. In this review, examples of protein modelling are taken from the Rh, RHAG, Kell, LW, Lutheran, Duffy, Dombrock and RAPH blood group systems.
红细胞表面膜含有多种蛋白质,其中许多由于其糖链或氨基酸序列的变化而表现出血型活性。为了了解血型抗原的性质、表达它们的蛋白质的功能以及它们之间的关系,人们采用计算机建模来预测它们的结构。当感兴趣的蛋白质的实验结构数据缺失或不完整时,建模是首选的极好方法。然后,可以使用模型来解释以前的实验数据并指导未来的实验。在这篇综述中,从 Rh、RHAG、Kell、LW、Lutheran、Duffy、Dombrock 和 RAPH 血型系统中选取了蛋白质建模的例子。