Dixit S N, Seyer J M, Kang A H
J Biol Chem. 1982 May 10;257(9):4864-8.
This communication describes the immunochemical and biochemical characterization of three polypeptide chains, alpha 1(IV)130K, alpha 1(IV)110K, and alpha 1(IV)75K belonging to the alpha 1(IV) chain of basement membrane collagen isolated from a pepsin digest of bovine kidney cortices. From the CNBr digests of the mixture of these chain fragments three peptides, a major and two minor peptides with an apparent Mr = 32,000, 24,000 and 13,000, respectively, were purified and characterized. The data presented show that CNBr peptides 24K and 13K are generated from CNBr peptide 32K by pepsin cleavage in the native molecule at the NH2-terminal end. Antisera were raised in rabbits against peptide CB32K. Inhibition assays using enzyme-linked immunoadsorbant assays (ELISA) showed cross-reactivity with alpha 1(IV)130K, alpha 1(IV)110K and alpha 1(IV)75K fragments. Peptides CB24K and 13K also inhibited the antiserum. Antiserum was not active when tested against alpha 1(IV)95K, alpha 1(IV)55K, alpha 2(IV)120K, and alpha 2(IV)95K fragments as inhibitors. These studies provide further evidence that alpha 1(IV)130K, 110K, and 75K are derived from the same parent chain. The pepsin cleavage sites resulting in the formation of these fragments and their internal alignment are described.
本通讯描述了从牛肾皮质胃蛋白酶消化物中分离出的基底膜胶原蛋白α1(IV)链的三条多肽链α1(IV)130K、α1(IV)110K和α1(IV)75K的免疫化学和生物化学特征。从这些链片段混合物的溴化氰消化物中,纯化并鉴定了三种肽,一种主要肽和两种次要肽,其表观分子量分别为32,000、24,000和13,000。所呈现的数据表明,溴化氰肽24K和13K是由溴化氰肽32K在天然分子的NH2末端经胃蛋白酶切割产生的。用针对肽CB32K的兔抗血清进行了实验。使用酶联免疫吸附测定(ELISA)的抑制试验表明,该抗血清与α1(IV)130K、α1(IV)110K和α1(IV)75K片段有交叉反应性。肽CB24K和13K也能抑制该抗血清。当作为抑制剂针对α1(IV)95K、α1(IV)55K、α2(IV)120K和α2(IV)95K片段进行测试时,抗血清无活性。这些研究进一步证明α1(IV)130K、110K和75K来自同一条母链。描述了导致这些片段形成的胃蛋白酶切割位点及其内部排列。