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如何使用 MixMHC2pred 预测新 MHC-II 等位基因的结合特异性和配体

How to Predict Binding Specificity and Ligands for New MHC-II Alleles with MixMHC2pred.

机构信息

Department of Oncology UNIL CHUV, Ludwig Institute for Cancer Research, University of Lausanne, Lausanne, Switzerland.

Swiss Institute of Bioinformatics (SIB), Lausanne, Switzerland.

出版信息

Methods Mol Biol. 2024;2809:215-235. doi: 10.1007/978-1-0716-3874-3_14.

Abstract

MHC-II molecules are key mediators of antigen presentation in vertebrate species and bind to their ligands with high specificity. The very high polymorphism of MHC-II genes within species and the fast-evolving nature of these genes across species has resulted in tens of thousands of different alleles, with hundreds of new alleles being discovered yearly through large sequencing projects in different species. Here we describe how to use MixMHC2pred to predict the binding specificity of any MHC-II allele directly from its amino acid sequence. We then show how both MHC-II ligands and CD4 T cell epitopes can be predicted in different species with our approach. MixMHC2pred is available at http://mixmhc2pred.gfellerlab.org/ .

摘要

MHC-II 分子是脊椎动物物种中抗原呈递的关键介质,它们与配体具有高度特异性结合。在物种内,MHC-II 基因具有非常高的多态性,而这些基因在物种间的快速进化特性导致了数万个不同的等位基因,每年通过不同物种的大型测序项目都会发现数百个新的等位基因。在这里,我们描述了如何使用 MixMHC2pred 直接从 MHC-II 等位基因的氨基酸序列预测其结合特异性。然后,我们展示了如何使用我们的方法在不同物种中预测 MHC-II 配体和 CD4 T 细胞表位。MixMHC2pred 可在 http://mixmhc2pred.gfellerlab.org/ 获得。

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