An Interaction-based Approach for Affinity Prediction between Antigen Peptide and Human Leukocyte Antigen Using COMBINE Analysis

IF 0.4 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Shinya Nakamura, Rie Ohmura, I. Nakanishi
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引用次数: 2

Abstract

In peptide vaccine therapy, a peptide with high affinity for human leukocyte antigen (HLA), is important to stimulate the immune system to kill cancer cells. Several methods to predict HLA–peptide binding have been reported, but most of them rely on informatics to analyze the amino acid sequence of the peptide. Although intermolecular-interaction-based analysis is expected to improve prediction accuracy, such a method generally involves a high computational cost. Therefore, comparative binding energy (COMBINE) analysis, a 3D-quantitative structure–activity relationship method, combined with a rapidly implemented protein modeling method, was applied to solve this problem. The new method enabled quick evaluation of peptide affinity predictions with accuracy beyond a statistical method. In addition, several amino acid residues of HLA, which are known to be important for peptide binding, could be identified.
结合分析抗原肽与人白细胞抗原亲和预测的相互作用方法
在肽疫苗治疗中,一种对人类白细胞抗原(HLA)具有高亲和力的肽对于刺激免疫系统杀死癌细胞非常重要。目前已经报道了几种预测hla -肽结合的方法,但大多数方法依赖于信息学分析肽的氨基酸序列。尽管基于分子间相互作用的分析有望提高预测精度,但这种方法通常涉及较高的计算成本。因此,采用比较结合能(COMBINE)分析,一种三维定量的构效关系方法,结合一种快速实现的蛋白质建模方法来解决这一问题。新方法能够快速评估肽亲和力预测,其准确性超过统计方法。此外,可以鉴定出HLA的几个氨基酸残基,这些氨基酸残基已知对肽结合很重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Chem-Bio Informatics Journal
Chem-Bio Informatics Journal BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
0.60
自引率
0.00%
发文量
8
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