Amari Shinji, Kataoka Ryoichi, Ikegami Takashi, Hirayama Noriaki
Science and Technology Systems Division, Computational Science Department, Ryoka Systems Inc., 1-1-2 Oshiage, Sumida-ku, Tokyo 131-0045, Japan.
Basic Medical Science and Molecular Medicine, Tokai University School of Medicine, 147 Shimokasuya, Isehara, Kanagawa 259-1143, Japan.
Int J Med Chem. 2013;2013:690513. doi: 10.1155/2013/690513. Epub 2013 Nov 27.
The three-dimensional (3D) structures of human leukocyte antigen (HLA) molecules are indispensable for the studies on the functions at molecular level. We have developed a homology modeling system named HLA-modeler specialized in the HLA molecules. Segment matching algorithm is employed for modeling and the optimization of the model is carried out by use of the PFROSST force field considering the implicit solvent model. In order to efficiently construct the homology models, HLA-modeler uses a local database of the 3D structures of HLA molecules. The structure of the antigenic peptide-binding site is important for the function and the 3D structure is highly conserved between various alleles. HLA-modeler optimizes the use of this structural motif. The leave-one-out cross-validation using the crystal structures of class I and class II HLA molecules has demonstrated that the rmsds of nonhydrogen atoms of the sites between homology models and crystal structures are less than 1.0 Å in most cases. The results have indicated that the 3D structures of the antigenic peptide-binding sites can be reproduced by HLA-modeler at the level almost corresponding to the crystal structures.
人类白细胞抗原(HLA)分子的三维(3D)结构对于分子水平的功能研究不可或缺。我们开发了一个专门针对HLA分子的同源建模系统,名为HLA-modeler。采用片段匹配算法进行建模,并使用考虑隐式溶剂模型的PFROSST力场对模型进行优化。为了高效构建同源模型,HLA-modeler使用了HLA分子3D结构的本地数据库。抗原肽结合位点的结构对其功能很重要,并且该3D结构在各种等位基因之间高度保守。HLA-modeler优化了这种结构基序的使用。使用I类和II类HLA分子的晶体结构进行的留一法交叉验证表明,在大多数情况下,同源模型与晶体结构之间位点的非氢原子均方根偏差(rmsds)小于1.0 Å。结果表明,HLA-modeler能够在几乎与晶体结构相当的水平上重现抗原肽结合位点的3D结构。