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人自然杀伤细胞受体NKR-P1可溶性形式在HEK293S GnTI细胞中的高效表达与纯化

High-level expression and purification of soluble form of human natural killer cell receptor NKR-P1 in HEK293S GnTI cells.

作者信息

Bláha Jan, Kalousková Barbora, Skořepa Ondřej, Pažický Samuel, Novák Petr, Vaněk Ondřej

机构信息

Department of Biochemistry, Faculty of Science, Charles University, Hlavova 2030/8, 12840 Prague, Czech Republic.

Department of Biochemistry, Faculty of Science, Charles University, Hlavova 2030/8, 12840 Prague, Czech Republic; Institute of Microbiology, The Czech Academy of Sciences, BIOCEV, Průmyslová 595, 25250 Vestec, Czech Republic.

出版信息

Protein Expr Purif. 2017 Dec;140:36-43. doi: 10.1016/j.pep.2017.07.016. Epub 2017 Jul 27.

Abstract

Human natural killer receptor protein 1 (NKR-P1, CD161, gene klrb1) is a C-type lectin-like receptor of natural killer (NK) cells responsible for recognition of its cognate protein ligand lectin-like transcript 1 (LLT1). NKR-P1 is the single human orthologue of the prototypical rodent NKR-P1 receptors. Naturally, human NKR-P1 is expressed on the surface of NK cells, where it serves as inhibitory receptor; and on T and NKT cells functioning as co-stimulatory receptor promoting secretion of IFNγ. Most notably, it is expressed on Th17 and Tc17 lymphocytes where presumably promotes targeting into LLT1 expressing immunologically privileged niches. We tested effect of different protein tags (SUMO, TRX, GST, MsyB) on expression of soluble NKR-P1 in E. coli. Then we optimized the expression construct of soluble NKR-P1 by preparing a library of expression constructs in pOPING vector containing the extracellular lectin-like domain with different length of the putative N-terminal stalk region and tested its expression in Sf9 and HEK293 cells. Finally, a high-level expression of soluble NKR-P1 was achieved by stable expression in suspension-adapted HEK293S GnTI cells utilizing pOPINGTTneo expression vector. Purified soluble NKR-P1 is homogeneous, deglycosylatable, crystallizable and monomeric in solution, as shown by size-exclusion chromatography, multi-angle light scattering and analytical ultracentrifugation.

摘要

人类自然杀伤细胞受体蛋白1(NKR-P1,CD161,基因klrb1)是自然杀伤(NK)细胞的一种C型凝集素样受体,负责识别其同源蛋白配体凝集素样转录物1(LLT1)。NKR-P1是典型啮齿动物NKR-P1受体的唯一人类同源物。自然情况下,人类NKR-P1在NK细胞表面表达,作为抑制性受体发挥作用;在T细胞和NKT细胞上表达,作为共刺激受体促进IFNγ的分泌。最值得注意的是,它在Th17和Tc17淋巴细胞上表达,可能促进靶向进入表达LLT1的免疫特权微环境。我们测试了不同蛋白标签(SUMO、TRX、GST、MsyB)对大肠杆菌中可溶性NKR-P1表达的影响。然后,我们通过构建一个包含不同长度推定N端茎区的细胞外凝集素样结构域的pOPING载体表达构建体文库,优化了可溶性NKR-P1的表达构建体,并测试了其在Sf9和HEK293细胞中的表达。最后,利用pOPINGTTneo表达载体在悬浮适应的HEK293S GnTI细胞中稳定表达,实现了可溶性NKR-P1的高水平表达。通过尺寸排阻色谱、多角度光散射和分析超速离心表明,纯化的可溶性NKR-P1在溶液中是均匀的、可去糖基化化的、可结晶的且为单体形式。

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