Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.
Protein Eng Des Sel. 2011 Sep;24(9):701-9. doi: 10.1093/protein/gzr035. Epub 2011 Jul 13.
Reliable and robust systems for engineering functional major histocompatibility complex class II (MHCII) proteins have proved elusive. Availability of such systems would enable the engineering of peptide-MHCII (pMHCII) complexes for therapeutic and diagnostic applications. In this paper, we have developed a system based on insect cell surface display that allows functional expression of heterodimeric DR2 molecules with or without a covalently bound human myelin basic protein (MBP) peptide, which is amenable to directed evolution of DR2-MBP variants with improved T cell receptor (TCR)-binding affinity. This study represents the first example of functional display of human pMHCII complexes on insect cell surface. In the process of developing this pMHCII engineering system, we have also explored the potential of using yeast surface display for the same application. Our data suggest that yeast display is a useful system for analysis and engineering of peptide binding of MHCII proteins, but not suitable for directed evolution of pMHC complexes that bind with low affinity to self-reactive TCRs.
可靠且稳健的工程功能性主要组织相容性复合体 II 类 (MHCII) 蛋白的系统一直难以实现。此类系统的可用性将能够为治疗和诊断应用工程化肽-MHCII (pMHCII) 复合物。在本文中,我们开发了一种基于昆虫细胞表面展示的系统,该系统允许功能性表达具有或不具有共价结合的人髓鞘碱性蛋白 (MBP) 肽的异二聚体 DR2 分子,该系统可用于定向进化具有改善的 T 细胞受体 (TCR) 结合亲和力的 DR2-MBP 变体。这项研究代表了在昆虫细胞表面功能性展示人 pMHCII 复合物的首例。在开发这种 pMHCII 工程系统的过程中,我们还探索了使用酵母表面展示进行相同应用的可能性。我们的数据表明,酵母展示是分析和工程 MHCII 蛋白肽结合的有用系统,但不适合结合低亲和力自身反应性 TCR 的 pMHC 复合物的定向进化。