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二硫键还原剂对海星中1-甲基腺嘌呤诱导的卵母细胞成熟的协同作用。

Synergistic actions of disulfide-reducing agents on 1-methyladenine-induced oocyte maturation in starfish.

作者信息

Yoshikuni M, Ishikawa K, Isobe M, Goto T, Nagahama Y

机构信息

Department of Developmental Biology, National Institute for Basic Biology, Okazaki, Japan.

出版信息

Dev Biol. 1988 Jul;128(1):236-9. doi: 10.1016/0012-1606(88)90285-0.

Abstract

Several disulfide-reducing agents, such as dithiothreitol, 2,3-dimercapto-1-propanol, cysteine ethyl ester, and cysteine methyl ester enhanced the effectiveness of 1-methyladenine (1-MeAde) to induce oocyte maturation in the starfish Asterina pectinifera. This enhancement occurred at relatively low concentrations at which these agents by themselves were ineffective in inducing oocyte maturation. The agents caused a marked (about twofold) increase in specific [1-3H]MeAde binding. The binding increased directly in relation to the potency of the agents in enhancing 1-MeAde action. Scatchard analysis indicated that dithiothreitol increased the Bmax without affecting the affinity of 1-MeAde binding. These results strongly suggest that disulfide-reducing agents enhance the maturational action of 1-MeAde by increasing the number of 1-MeAde binding sites in oocyte cortices.

摘要

几种二硫键还原剂,如二硫苏糖醇、2,3-二巯基-1-丙醇、半胱氨酸乙酯和半胱氨酸甲酯,可增强1-甲基腺嘌呤(1-MeAde)诱导日本海星(Asterina pectinifera)卵母细胞成熟的效果。这种增强作用在相对较低的浓度下就会出现,而在这些浓度下,这些试剂本身并不能诱导卵母细胞成熟。这些试剂使特异性[1-³H]MeAde结合显著增加(约两倍)。结合增加与试剂增强1-MeAde作用的效力直接相关。Scatchard分析表明,二硫苏糖醇增加了Bmax,但不影响1-MeAde结合的亲和力。这些结果有力地表明,二硫键还原剂通过增加卵母细胞皮质中1-MeAde结合位点的数量来增强1-MeAde的成熟作用。

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