Techniques for Theoretical Prediction of Immunogenic Peptides

Robert Friedman
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Abstract

Small peptides are an important component of the vertebrate immune system. They are important molecules for distinguishing proteins that originate in the host from proteins derived from a pathogenic organism, such as a virus or bacterium. Consequently, these peptides are central for the vertebrate host response to intracellular and extracellular pathogens. Computational models for prediction of these peptides have been based on a narrow sample of data with an emphasis on the position and chemical properties of the amino acids. In past literature, this approach has resulted in higher predictability than models that rely on the geometrical arrangement of atoms. However, protein structure data from experiment and theory are a source for building models at scale, and, therefore, knowledge on the role of small peptides and their immunogenicity in the vertebrate immune system. The following sections introduce procedures that contribute to theoretical prediction of peptides and their role in immunogenicity. Lastly, deep learning is discussed as it applies to immunogenetics and the acceleration of knowledge by a capability for modeling the complexity of natural phenomena.
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免疫原肽的理论预测技术
小肽是脊椎动物免疫系统的重要组成部分。它们是区分宿主体内的蛋白质和来自病毒或细菌等病原体的蛋白质的重要分子。因此,这些肽是脊椎动物宿主应对细胞内和细胞外病原体的核心。预测这些肽的计算模型一直是基于狭窄的数据样本,重点是氨基酸的位置和化学性质。在过去的文献中,这种方法比依赖原子几何排列的模型具有更高的可预测性。然而,来自实验和理论的蛋白质结构数据是建立大规模模型的源泉,因此也是了解小肽在脊椎动物免疫系统中的作用及其免疫原性的源泉。下文将介绍有助于理论预测多肽及其免疫原性作用的程序。最后,将讨论深度学习在免疫遗传学中的应用,以及通过对复杂自然现象建模的能力来加速知识的发展。
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