Center for Translational Science, Florida International University, Port St. Lucie, Florida.
Nova Southeastern University, Fort Lauderdale, Florida.
Curr Protoc. 2022 Mar;2(3):e378. doi: 10.1002/cpz1.378.
This article presents a combinatorial library method that consists of the synthesis and screening of mixture-based synthetic combinatorial libraries of peptide molecules to identify B and T cell epitopes. The protocols employ peptide libraries to identify peptides recognized by MAbs and T cells. The first protocol uses a positional scanning peptide library made up of hexapeptides to identify antigenic determinants recognized by MAbs. The 120 mixtures in the hexapeptide library are tested for their inhibitory activity in a competitive ELISA. The second protocol uses a decapeptide library to identify T cell peptide ligands. The 200 mixtures of the decapeptide library are tested for their ability to induce T cell activation. Support protocols cover optimization of the assay conditions for each MAb or T cell, to achieve the best level of sensitivity and reproducibility, and preparation of a hexapeptide library, along with deconvolution approaches. © 2022 Wiley Periodicals LLC. Basic Protocol 1: Screening peptide library for antibody inhibition Basic Protocol 2: Screening a peptide library to identify CD4 Or CD8 T cell ligands Support Protocol 1: Optimizing antigen and antibody concentrations for screening assay Support Protocol 2: Preparing a positional scanning peptide library.
本文提出了一种组合文库方法,包括合成和筛选基于混合物的肽分子合成组合文库,以鉴定 B 和 T 细胞表位。该方案采用肽文库来鉴定被单抗和 T 细胞识别的肽。第一个方案使用由六肽组成的位置扫描肽文库来鉴定单抗识别的抗原决定簇。在竞争性 ELISA 中测试六肽文库中的 120 种混合物的抑制活性。第二个方案使用十肽文库来鉴定 T 细胞肽配体。测试 200 种十肽文库混合物诱导 T 细胞激活的能力。支持方案涵盖了优化每个单抗或 T 细胞的测定条件,以达到最佳的灵敏度和重现性,并制备六肽文库以及解码方法。© 2022 Wiley Periodicals LLC. 基本方案 1:筛选肽文库以检测抗体抑制 基本方案 2:筛选肽文库以鉴定 CD4 或 CD8 T 细胞配体 支持方案 1:优化筛选测定中的抗原和抗体浓度 支持方案 2:制备位置扫描肽文库。