将II类MHC结合基序转化为定量预测模型的迭代算法。

R R Mallios
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引用次数: 4

摘要

生物化学家和分子生物学家已经根据实验室结果和晶体结构提出了描述肽片段和II类主要组织相容性复合体(MHC)分子结合的基序。本文提出的迭代算法将建议的基序转换为基于定量数据的模型。所访问的数据库由已知与特定单倍型的II类MHC分子结合或不结合的肽片段组成。逐步判别分析利用增加或减少基序系数,直到得到的基序正确分类所有结合物和非结合物。逐步判别分析是一个标准的多元统计程序,并可在全面的商业统计软件包。本研究采用BMDP统计软件中的7M程序。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An iterative algorithm for converting a class II MHC binding motif into a quantitative predictive model.

Biochemists and molecular biologists have suggested motifs for characterizing the binding of peptide fragments and class II major histocompatibility complex (MHC) molecules based on laboratory results and crystal structures. The iterative algorithm presented here converts a suggested motif into a quantitative data-based model. The database accessed consists of peptide fragments known to bind or not bind to class II MHC molecules of particular haplotypes. Stepwise discriminant analysis is utilized to increase or decrease motif coefficients until the resulting motif classifies all binders and non-binders correctly. Stepwise discriminant analysis is a standard multivariate statistical procedure and is available in comprehensive commercial statistical packages. Program 7M of BMDP Statistical Software was used in this study.

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