T细胞受体
生物
底漆(化妆品)
基因
遗传学
BETA(编程语言)
计算生物学
分子生物学
T细胞
免疫系统
计算机科学
有机化学
化学
程序设计语言
作者
Angela Chiew Wen Ch’ng,Soo Khim Chan,Joshua Ignatius,Theam Soon Lim
标识
DOI:10.1002/eji.201747328
摘要
Abstract The application of human TCR in cancer immunotherapy has gained momentum with developments in tumor killing strategies using endogenous adaptive immune responses. The successful coverage of a diverse TCR repertoire is mainly attributed to the primer design of the human TCR V genes. Here, we present a refined primer design strategy of the human TCR V gene by clustering V gene sequence homolog for degenerate primer design based on the data from IMGT. The primers designed were analyzed and the PCR efficiency of each primer set was optimized. A total of 112 alpha and 160 beta sequences were aligned and clustered using a phylogram yielding 32 and 27 V gene primers for the alpha and beta family. The new primer set was able to provide 93.75% and 95.63% coverage for the alpha and beta family, respectively. A semi‐qualitative approach using the designed primer set was able to provide a relative view of the TCR V gene diversity in different populations. Taken together, the new primers provide a more comprehensive coverage of the TCR gene diversity for improved TCR library generation and TCR V gene analysis studies.
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