Leyton-Castro Nestor F, Brigido Marcelo M, Maranhão Andrea Q
Molecular Pathology Graduation Programme, School of Medicine, University of Brasilia, Brasilia, Brazil.
Department of Cell Biology, Institute of Biological Sciences, University of Brasilia, Brasilia, Brazil.
Methods Mol Biol. 2020;2086:13-26. doi: 10.1007/978-1-0716-0146-4_2.
CAR-T cell therapy emerged in the last years as a great promise to cancer treatment. Nowadays, there is a run to improve the breadth of its use, and thus, new chimeric antigen receptors (CAR) are being proposed. The antigen-binding counterpart of CAR is an antibody fragment, scFv (single chain variable fragment), that recognizes a membrane protein associated to a cancer cell. In this chapter, the use of human scFv phage display libraries as a source of new mAbs against surface antigen is discussed. Protocols focusing in the use of extracellular domains of surface protein in biotinylated format are proposed as selection antigen. Elution with unlabeled peptide and selection in solution is described. The analysis of enriched scFvs throughout the selection using NGS is also outlined. Taken together these protocols allow for the isolation of new scFvs able to be useful in the construction of new chimeric antigen receptors for application in cancer therapy.
嵌合抗原受体(CAR)T细胞疗法在过去几年中成为癌症治疗的巨大希望。如今,人们竞相扩大其应用范围,因此提出了新的嵌合抗原受体(CAR)。CAR的抗原结合部分是一个抗体片段,即单链可变片段(scFv),它识别与癌细胞相关的膜蛋白。在本章中,将讨论使用人scFv噬菌体展示文库作为针对表面抗原的新单克隆抗体的来源。提出了以生物素化形式使用表面蛋白细胞外结构域作为选择抗原的方案。描述了用未标记肽洗脱和在溶液中进行选择的方法。还概述了使用NGS对整个筛选过程中富集的scFv进行分析。综合这些方案,可以分离出新的scFv,这些scFv可用于构建用于癌症治疗的新嵌合抗原受体。