Haralson M A, Mitchell W M, Rhodes R K, Miller E J
Arch Biochem Biophys. 1984 Mar;229(2):509-18. doi: 10.1016/0003-9861(84)90182-6.
The collagenous protein synthesized by cultured Chinese hamster lung (CHL) cells and present in the culture medium has been isolated after limited pepsin digestion and differential salt precipitation. Molecular size analysis of this material indicates that the CHL cell medium collagen contains chains which exhibit an apparent molecular mass of approximately 85,000 Da. When chromatographed on CM-cellulose under denaturing conditions, the reduced and alkylated CHL cell medium collagen chains elute slightly after the human alpha1(I) chain but well before the pepsin-derived alpha1(V) chain, which is the constituent chain present in the CHL cell cellular matrix collagen. Analysis of the peptides derived by CNBr cleavage of the CHL medium collagen chains by chromatography on CM-cellulose reveals, however, that these chains contain peptides which correspond both in size and in chemical properties to those derived from the alpha1(V) collagen chain, but clearly lack two peptides (alpha1(V)-CB4 and alpha1(V)-CB5) which are normally present in pepsin-derived alpha1(V) chains. Furthermore, analysis of the CHL cell culture medium collagenous material obtained without pepsin digestion indicates the presence of collagenous chains that exhibit after reduction a molecular mass of approximately 160,000 Da, which is smaller than the proposed size of the pro alpha1(V) collagen chain. These results demonstrate that the collagenous protein present in the culture medium of CHL cells is directly related at the primary structural level to the alpha1(V) collagen chain, and it is postulated that this material represents the large fragment derived from a collagenase cleavage of the [pro alpha1(V)]3 molecules present in the cell layer. Furthermore, these results and previous reports indicate that the only identifiable genetic type of procollagen chain synthesized by this cloned cell line in culture corresponds to the pro alpha1(V) chain.
通过培养的中国仓鼠肺(CHL)细胞合成并存在于培养基中的胶原蛋白,经有限的胃蛋白酶消化和分级盐沉淀后已被分离出来。对该物质的分子大小分析表明,CHL细胞培养基胶原蛋白包含的链的表观分子量约为85,000道尔顿。当在变性条件下于CM - 纤维素上进行色谱分析时,还原和烷基化后的CHL细胞培养基胶原蛋白链在人α1(I)链之后略微洗脱,但远在胃蛋白酶衍生的α1(V)链之前洗脱,α1(V)链是CHL细胞细胞基质胶原蛋白中的组成链。然而,通过在CM - 纤维素上进行色谱分析对CHL培养基胶原蛋白链经溴化氰裂解得到的肽段进行分析发现,这些链包含的肽段在大小和化学性质上均与源自α1(V)胶原蛋白链的肽段相对应,但明显缺少通常存在于胃蛋白酶衍生的α1(V)链中的两个肽段(α1(V) - CB4和α1(V) - CB5)。此外,对未经胃蛋白酶消化获得的CHL细胞培养基胶原物质的分析表明,存在还原后分子量约为160,000道尔顿的胶原链,这比推测的前α1(V)胶原蛋白链的大小要小。这些结果表明,CHL细胞培养基中存在的胶原蛋白在一级结构水平上与α1(V)胶原蛋白链直接相关,据推测该物质代表了细胞层中存在的[前α1(V)]3分子经胶原酶裂解产生的大片段。此外,这些结果和先前的报道表明,该克隆细胞系在培养中合成的唯一可识别的原胶原链遗传类型对应于前α1(V)链。