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计算方法预测构象 B 细胞表位。

Computational Methods to Predict Conformational B-Cell Epitopes.

机构信息

Department of Chemistry and Biochemistry, Yeshiva College, Yeshiva University, New York, NY 10033, USA.

出版信息

Biomolecules. 2024 Aug 10;14(8):983. doi: 10.3390/biom14080983.

Abstract

Accurate computational prediction of B-cell epitopes can greatly enhance biomedical research and rapidly advance efforts to develop therapeutics, monoclonal antibodies, vaccines, and immunodiagnostic reagents. Previous research efforts have primarily focused on the development of computational methods to predict linear epitopes rather than conformational epitopes; however, the latter is much more biologically predominant. Several conformational B-cell epitope prediction methods have recently been published, but their predictive performances are weak. Here, we present a review of the latest computational methods and assess their performances on a diverse test set of 29 non-redundant unbound antigen structures. Our results demonstrate that ISPIPab performs better than most methods and compares favorably with other recent antigen-specific methods. Finally, we suggest new strategies and opportunities to improve computational predictions of conformational B-cell epitopes.

摘要

准确的 B 细胞表位计算预测可以极大地促进生物医学研究,并快速推进治疗方法、单克隆抗体、疫苗和免疫诊断试剂的开发。以前的研究工作主要集中在开发用于预测线性表位的计算方法上,而不是构象表位;然而,后者在生物学上更为重要。最近已经发表了几种构象 B 细胞表位预测方法,但它们的预测性能较弱。在这里,我们对最新的计算方法进行了综述,并在一个由 29 个非冗余未结合抗原结构组成的多样化测试集上评估了它们的性能。我们的结果表明,ISPIPab 的性能优于大多数方法,并与其他最近的抗原特异性方法相比具有优势。最后,我们提出了改进构象 B 细胞表位计算预测的新策略和机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/257d/11352882/5fb7b31a096e/biomolecules-14-00983-g001.jpg

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