主要组织相容性复合体
抗原处理
MHC I级
抗原呈递
生物
介绍(产科)
计算生物学
免疫学
抗原
免疫系统
T细胞
医学
放射科
作者
Ida Hafstrand,Aure Aflalo,Louise H. Boyle
标识
DOI:10.1016/j.coi.2021.04.011
摘要
The peptide editor TAPBPR is the newest member of the major histocompatibility complex class I (MHC-I) antigen processing and presentation pathway. Since 2013, studies have explored the functions and mechanisms of action of this tapasin homolog. Here, we review the key insights gained from structural studies of the TAPBPR:MHC-I complex and the involvement of the TAPBPR loop in peptide exchange. However, despite recent advances, the question still remains: why do we need TAPBPR? The recent appreciation that different MHC-I allotypes vary in their ability to interact with TAPBPR, together with a role for TAPBPR in alternative presentation pathways highlights that much remains unknown concerning the biological need for TAPBPR.
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