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免疫亲和纯化IM-9成淋巴细胞P物质受体的膜蛋白成分。

Immunoaffinity purification of membrane protein constituents of the IM-9 lymphoblast receptor for substance P.

作者信息

McGillis J P, Organist M L, Payan D G

机构信息

Howard Hughes Medical Institute, San Francisco, California.

出版信息

Anal Biochem. 1987 Aug 1;164(2):502-13. doi: 10.1016/0003-2697(87)90525-2.

Abstract

Substance P (SP) is an undecapeptide neuromediator that stimulates human T-lymphocyte function by binding to stereospecific membrane receptors. Human IM-9 cultured B-lymphoblasts express approximately 20,000 receptors per cell for [125I]SP with a Kd of 0.3 nM. [125I]SP was specifically crosslinked by disuccinimidyl suberate to IM-9 cell membrane proteins of 78, 58, and 33 kDa. An indirect immunoaffinity purification procedure has now been developed based on immunoabsorption of detergent-solubilized [125I]SP-labeled IM-9 cell membrane proteins to anti-SP antibody that was bound to an epoxide ultraffinity high-performance liquid chromatography column, followed by elution in acidic 8 M urea. The 58- and 33-kDa SP-receptor complexes were purified to apparent homogeneity by immunoaffinity chromatography and identified by autoradiography and silver staining of sodium dodecyl sulfate-polyacryl-amide gels.

摘要

P物质(SP)是一种十一肽神经介质,它通过与立体特异性膜受体结合来刺激人T淋巴细胞功能。人IM - 9培养的B淋巴母细胞每个细胞表达约20,000个[125I]SP受体,解离常数(Kd)为0.3 nM。[125I]SP通过辛二酸二琥珀酰亚胺酯与78、58和33 kDa的IM - 9细胞膜蛋白特异性交联。现在已经开发出一种间接免疫亲和纯化方法,该方法基于将去污剂溶解的[125I]SP标记的IM - 9细胞膜蛋白免疫吸附到与环氧超亲和高效液相色谱柱结合的抗SP抗体上,然后在酸性8 M尿素中洗脱。通过免疫亲和色谱将58 kDa和33 kDa的SP受体复合物纯化至表观均一性,并通过放射自显影和十二烷基硫酸钠 - 聚丙烯酰胺凝胶的银染进行鉴定。

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