High-level expression and purification of soluble form of human natural killer cell receptor NKR-P1 in HEK293S GnTI- cells
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
PubMed
28757467
DOI
10.1016/j.pep.2017.07.016
PII: S1046-5928(17)30333-9
Knihovny.cz E-zdroje
- Klíčová slova
- CD161, HEK293, LLT1, NK cells, NKR-P1, klrb1,
- MeSH
- bioreaktory MeSH
- buňky NK metabolismus MeSH
- buňky Th17 metabolismus MeSH
- Escherichia coli genetika MeSH
- HEK293 buňky MeSH
- lektinové receptory NK-buněk - podrodina B biosyntéza genetika izolace a purifikace MeSH
- lektiny typu C metabolismus MeSH
- lidé MeSH
- ligandy MeSH
- receptory buněčného povrchu metabolismus MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- CLEC2D protein, human MeSH Prohlížeč
- KLRB1 protein, human MeSH Prohlížeč
- lektinové receptory NK-buněk - podrodina B MeSH
- lektiny typu C MeSH
- ligandy MeSH
- receptory buněčného povrchu MeSH
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.
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