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小鼠垂体细胞培养物中促肾上腺皮质激素和内啡肽常见前体形式的加工过程中涉及的步骤。

Steps involved in the processing of common precursor forms of adrenocorticotropin and endorphin in cultures of mouse pituitary cells.

作者信息

Roberts J L, Phillips M, Rosa P A, Herbert E

出版信息

Biochemistry. 1978 Aug 22;17(17):3609-18. doi: 10.1021/bi00610a030.

Abstract

The initial steps in the processing of the common precursor to adrenocorticotropin (ACTH) and endorphin in mouse pituitary tumor cells (AtT-20) have been investigated. Three forms of the precursor have been resolved by sodium dodecyl sulfate (NaDodSO4)-polyacrylamide gel electrophoresis with apparent molecular weights of 29 000 (29K ACTH-endorphin), 32 000 (32K ACTH-endorphin) and 34 000 (34K ACTH-endorphin). These forms have a similar peptide backbone, but their carbohydrate content differs. In particular, a tryptic glycopeptide has been observed in 32K ACTH-endorphin which is not present in 29K ACTH-endorphin and has been identified as the tryptic peptide containing the alpha(22--39) sequence of ACTH. Similar heterogeneity in carbohydrate has been observed in some of the smaller molecular weight forms of ACTH which are resolved by NaDodSO4 gel electrophoresis. Pulse chase and continuous labeling studies using radioactive amino acids and sugars suggest that the 29K ACTH-endorphin is converted to 32K and 34K ACTH-endorphin by the addition of carbohydrate. The glycopeptide and pulse chase studies suggest that 29K ACTH-endorphin is at a branch point in the processing pathways. It can either be converted to 4.5K ACTH by proteolytic processing or to 32K ACTH-endorphin by the further addition of carbohydrate. The 32K ACTH-endorphin can then be converted to 13K ACTH, the glycosylated form of 4.5K ACTH (Eipper, B.A., & Mains,, R.E. (1977) J.Biol. Chem.252, 882), by proteolytic processing. A comparison of the distribution of the different molecular weight forms of ACTH and endorphin in mouse pituitary extracts and in the mouse pituitary tumor cells reveals that the pituitary contains all of the forms of ACTH and endorphin seen in the tumor cells, including the three forms of the ACTH-endorphin precursor. However, the molecular weight distribution of the forms in the anterior lobe is very different from that in the intermediate lobe of mouse pituitary.

摘要

对小鼠垂体瘤细胞(AtT-20)中促肾上腺皮质激素(ACTH)和内啡肽共同前体的加工初始步骤进行了研究。通过十二烷基硫酸钠(NaDodSO4)-聚丙烯酰胺凝胶电泳分离出前体的三种形式,其表观分子量分别为29000(29K ACTH-内啡肽)、32000(32K ACTH-内啡肽)和34000(34K ACTH-内啡肽)。这些形式具有相似的肽骨架,但碳水化合物含量不同。特别是,在32K ACTH-内啡肽中观察到一种胰蛋白酶糖肽,而在29K ACTH-内啡肽中不存在,并且已被鉴定为含有ACTH的α(22 - 39)序列的胰蛋白酶肽。在通过NaDodSO4凝胶电泳分离的一些较小分子量的ACTH形式中也观察到了类似的碳水化合物异质性。使用放射性氨基酸和糖的脉冲追踪和连续标记研究表明,29K ACTH-内啡肽通过添加碳水化合物转化为32K和34K ACTH-内啡肽。糖肽和脉冲追踪研究表明,29K ACTH-内啡肽处于加工途径的分支点。它可以通过蛋白水解加工转化为4.5K ACTH,或者通过进一步添加碳水化合物转化为32K ACTH-内啡肽。然后,32K ACTH-内啡肽可以通过蛋白水解加工转化为13K ACTH,即4.5K ACTH的糖基化形式(Eipper,B.A.,& Mains,R.E.(1977)J.Biol.Chem.252,882)。对小鼠垂体提取物和小鼠垂体瘤细胞中不同分子量形式的ACTH和内啡肽分布的比较表明,垂体包含在肿瘤细胞中所见的所有ACTH和内啡肽形式,包括ACTH-内啡肽前体的三种形式。然而,前叶中这些形式的分子量分布与小鼠垂体中间叶中的非常不同。

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