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HL60细胞中两种不同肿瘤坏死因子受体的纯化及部分氨基酸序列分析

Purification and partial amino acid sequence analysis of two distinct tumor necrosis factor receptors from HL60 cells.

作者信息

Loetscher H, Schlaeger E J, Lahm H W, Pan Y C, Lesslauer W, Brockhaus M

机构信息

Central Research Units, F. Hoffmann-La Roche Ltd., Basel, Switzerland.

出版信息

J Biol Chem. 1990 Nov 25;265(33):20131-8.

PMID:2173696
Abstract

Two distinct tumor necrosis factor (TNF) receptors of 55- and 75-kDa apparent molecular masses previously identified on the cell surface by monoclonal antibodies have been solubilized with Triton X-100 from HL60 cells. A filter-based dot blot assay was developed to monitor specific 125I-TNF alpha binding during fractionation of the cell extract. By a combination of immuno- and ligand affinity chromatography and reverse phase high performance liquid chromatography both receptor proteins were purified to apparent homogeneity. Analysis by sodium dodecyl sulfate-polyacrylamide gel electrophoresis showed two bands at 55 and 51 kDa for the 55-kDa TNF receptor and a major 75-kDa and a minor 65-kDa band for the 75-kDa TNF receptor. All these bands specifically bound TNF alpha and TNF beta in ligand blot experiments. The exclusive specificity of monoclonal antibodies of the utr series for the 75.65-kDa bands and of the htr series for the 55.51-kDa bands was demonstrated with the purified antigens on Western blots. Both TNF receptor types were found to contain N-linked carbohydrates. N-terminal amino acid sequence analysis of the 55- and 51-kDa bands of the 55-kDa TNF receptor revealed identical sequences suggesting a possible truncation at the C-terminal end. Two different N-terminal sequences were determined for the 65-kDa band. One corresponded to the published sequence of ubiquitin; the other was therefore assumed to be a unique sequence of the 75-kDa TNF receptor. Additional internal sequences of this receptor were determined after proteolytic cleavage.

摘要

先前通过单克隆抗体在细胞表面鉴定出的两种表观分子量分别为55 kDa和75 kDa的不同肿瘤坏死因子(TNF)受体,已用Triton X-100从HL60细胞中溶解出来。开发了一种基于滤膜的斑点印迹分析方法,以监测细胞提取物分级分离过程中特异性的125I-TNFα结合。通过免疫亲和色谱、配体亲和色谱和反相高效液相色谱相结合的方法,两种受体蛋白均被纯化至表观均一。十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分析显示,55 kDa的TNF受体有两条带,分别位于55 kDa和51 kDa处;75 kDa的TNF受体有一条主要的75 kDa带和一条次要的65 kDa带。在配体印迹实验中,所有这些条带均能特异性结合TNFα和TNFβ。在蛋白质印迹上用纯化的抗原证明了utr系列单克隆抗体对75/65 kDa条带以及htr系列单克隆抗体对55/51 kDa条带的专一特异性。发现两种TNF受体类型均含有N-连接的碳水化合物。对55 kDa TNF受体的55 kDa和51 kDa条带进行N端氨基酸序列分析,结果显示序列相同,表明可能在C端发生了截短。对65 kDa条带确定了两种不同的N端序列。一种与已发表的泛素序列相对应;因此另一种被认为是75 kDa TNF受体的独特序列。在蛋白水解切割后确定了该受体的其他内部序列。

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