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人胎盘层粘连蛋白完整片段及胃蛋白酶衍生片段的分离、纯化与表征

Isolation, purification and characterization of intact and pepsin-derived fragments of laminin from human placenta.

作者信息

Dixit S N

出版信息

Connect Tissue Res. 1985;14(1):31-40. doi: 10.3109/03008208509089841.

Abstract

Human laminin, in intact form and as pepsin cleaved fragments, was isolated and purified from placenta. The intact laminin was extracted by 1-M NaCl at neutral pH in the presence of 10-mM EDTA and 3% Triton X-100. This recovered material was purified by DEAE-cellulose and agarose gel chromatography. The laminin fragments P1, P2 and P3 were prepared by limited pepsin proteolysis. Antibodies were prepared against fragment P2. The laminin and its fragments were characterized by amino acid composition, NaDoSO4-polyacrylamide gel electrophoresis and immunochemistry. Results from these studies show that substantial quantities of laminin can be prepared from placenta in this manner.

摘要

从胎盘中分离并纯化了完整形式以及经胃蛋白酶切割片段的人层粘连蛋白。完整的层粘连蛋白在中性pH值、10 mM乙二胺四乙酸(EDTA)和3% Triton X - 100存在的条件下,用1 M氯化钠提取。回收的物质通过二乙氨基乙基纤维素(DEAE - 纤维素)和琼脂糖凝胶色谱法进行纯化。层粘连蛋白片段P1、P2和P3通过有限的胃蛋白酶蛋白水解制备。制备了针对片段P2的抗体。通过氨基酸组成、十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳(NaDoSO4 - PAGE)和免疫化学对层粘连蛋白及其片段进行了表征。这些研究结果表明,通过这种方式可以从胎盘中制备出大量的层粘连蛋白。

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