Boulter Jonathan M, Glick Meir, Todorov Penio T, Baston Emma, Sami Malkit, Rizkallah Pierre, Jakobsen Bent K
Avidex Ltd. 57 Milton Park, Abingdon, Oxon OX14 4RX, UK.
Protein Eng. 2003 Sep;16(9):707-11. doi: 10.1093/protein/gzg087.
Antibody and T-cell receptors (TCRs) are the primary recognition molecules of the adaptive immune system. Antibodies have been extensively characterized and are being developed for a large number of therapeutic applications. This has been possible because of the ability to manufacture stable, soluble, monoclonal antibodies which retain the antigen specificity of B cells. Unlike antibodies, TCRs are not expressed in a soluble form, but are anchored to the T-cell surface by an insoluble trans-membrane domain. Characterization and development of TCRs has been hampered by the lack of suitable methods for producing them as soluble and stable proteins. Here we report the engineering of soluble human TCRs suitable for crystallization studies and potentially for in vivo therapeutic use.
抗体和T细胞受体(TCR)是适应性免疫系统的主要识别分子。抗体已得到广泛表征,并正被开发用于大量治疗应用。这之所以成为可能,是因为能够制造出保留B细胞抗原特异性的稳定、可溶性单克隆抗体。与抗体不同,TCR不以可溶性形式表达,而是通过不可溶的跨膜结构域锚定在T细胞表面。由于缺乏将TCR制备成可溶性和稳定蛋白质的合适方法,TCR的表征和开发受到了阻碍。在此,我们报告了适合结晶研究以及潜在体内治疗用途的可溶性人TCR的工程化。