Expression, Purification, and Crystallization of the Vγ9Vδ2 T-cell Receptor Recognizing Protein/Peptide Antigens

IF 1.9 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY The Protein Journal Pub Date : 2023-08-25 DOI:10.1007/s10930-023-10151-3
Chaofei Cheng, Zhendong Zhao, Guangzhi Liu
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Abstract

γδ T cells, especially Vγ9Vδ2 T cells, play an important role in mycobacterial infection. We have identified some Vγ9Vδ2 T cells that recognize protein/peptide antigens derived from mycobacteria, which may induce protective immune responses to mycobacterial infection. To clarify the structural basis of the molecular recognition mechanism, we tried many methods to express the Vγ9Vδ2 T-cell receptor (TCR). The Vγ9Vδ2 TCR was not expressed well in a prokaryotic expression system or a baculovirus expression system, even after extensive optimization. In a mammalian cell expression system, the Vγ9Vδ2 TCR was expressed in the form of a soluble heterodimer, which was suitable for crystal screening. Reduced-temperature cultivation (cold shock) increased the yield of the recombinant TCR. The recombinant purified TCR was used for crystal trials, and crystals that could be used for X-ray diffraction were obtained. Although we have not yet determined the crystal structure of the Vγ9Vδ2 TCR, we have established a procedure for Vγ9Vδ2 TCR expression and purification, which is useful for basic research and potentially for clinical application.

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Vγ9Vδ2 T细胞受体识别蛋白/肽抗原的表达、纯化和结晶。
γδT细胞,特别是Vγ9Vδ2 T细胞,在分枝杆菌感染中起着重要作用。我们已经鉴定了一些Vγ9Vδ2 T细胞,它们识别来自分枝杆菌的蛋白质/肽抗原,可能诱导对分枝杆菌感染的保护性免疫反应。为了阐明分子识别机制的结构基础,我们尝试了多种方法来表达Vγ9Vδ2 T细胞受体(TCR)。即使经过广泛的优化,Vγ9Vδ2 TCR在原核表达系统或杆状病毒表达系统中也不能很好地表达。在哺乳动物细胞表达系统中,Vγ9Vδ2 TCR以可溶性异二聚体的形式表达,适合于晶体筛选。低温培养(冷激)提高了重组TCR的产量。将重组纯化的TCR用于晶体试验,并获得可用于X射线衍射的晶体。虽然我们还没有确定Vγ9Vδ2 TCR的晶体结构,但我们已经建立了Vγ9Vδ2 TCR的表达和纯化程序,这对基础研究和临床应用都很有用。
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来源期刊
The Protein Journal
The Protein Journal 生物-生化与分子生物学
CiteScore
5.20
自引率
0.00%
发文量
57
审稿时长
12 months
期刊介绍: The Protein Journal (formerly the Journal of Protein Chemistry) publishes original research work on all aspects of proteins and peptides. These include studies concerned with covalent or three-dimensional structure determination (X-ray, NMR, cryoEM, EPR/ESR, optical methods, etc.), computational aspects of protein structure and function, protein folding and misfolding, assembly, genetics, evolution, proteomics, molecular biology, protein engineering, protein nanotechnology, protein purification and analysis and peptide synthesis, as well as the elucidation and interpretation of the molecular bases of biological activities of proteins and peptides. We accept original research papers, reviews, mini-reviews, hypotheses, opinion papers, and letters to the editor.
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