ISSN 0371-0874, CN 31-1352/Q

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小鼠精子热休克蛋白90的棕榈酰化

李瑞, 李坤, 杨岳, 孙培蓓, 陈爱君, 倪崖

温州医科大学检验医学院,生命科学学院,温州 325035;浙江省医学科学院生殖医学研究中心,杭州 310013

摘要

蛋白质棕榈酰化是指饱和十六碳的棕榈酸盐通过硫酯键或者酰胺键连接在蛋白质肽链的半胱氨酸上,属翻译后修饰,可影响蛋白质的相互作用、稳定性及定位等功能。热休克蛋白90 (heat shock protein 90, Hsp90)是一种重要的分子伴侣,已证明其参与精子获能等生理过程。然而,哺乳动物精子中是否存在蛋白质棕榈酰化,Hsp90在精子不同生理状态下是否发生棕榈酰化,目前尚不清楚。本研究首先采用酰基-生物素置换法检测小鼠附睾尾部成熟精子总蛋白质棕榈酰化情况,然后通过CSS-Palm 4.0软件预测Hsp90的棕榈酰化位点,再进一步结合免疫沉淀方法检测附睾头部、附睾尾部精子的Hsp90棕榈酰化情况。结果显示,小鼠附睾尾部精子多种蛋白质存在棕榈酰化,其中分子量大小约50、65、72、85和130 kDa的蛋白质发生棕榈酰化最为显著;软件预测显示Hsp90两个亚型共有5个棕榈酰化位点;免疫沉淀结果也显示小鼠精子存在棕榈酰化的Hsp90,且其棕榈酰化水平与小鼠精子的生理状态有关:附睾尾部棕榈酰化水平比附睾头部高,而获能后的棕榈酰化水平比获能前明显升高。以上结果表明,哺乳动物精子中存在蛋白棕榈酰化,且Hsp90棕榈酰化可能参与精子生理状态的调节。

关键词: 精子; 棕榈酰化; 酰基-生物素置换法; 热休克蛋白90

分类号:R169

[Palmitoylation of heat shock protein 90 in mouse sperm.] [Article in Chinese]

LI Rui, LI Kun, YANG Yue, SUN Pei-Bei, CHEN Ai-Jun, NI Ya

School of Laboratory Medicine and Life Science, Wenzhou Medical University, Wenzhou 325035, China; Center for Reproductive Medicine, Zhejiang Academy of Medical Sciences, Hangzhou 310013, China

Abstract

Protein palmitoylation, one of post-translation modifications, refers to the addition of saturated 16-carbon palmitic acid to cysteine residues via the thioester bond. It plays key roles in various functional activities, such as the interaction, stability and location of proteins. Heat shock protein 90 (Hsp90), an important molecular chaperone, has been reported to be involved in sperm capacitation. However, it remains unclear whether protein palmitoylation exists in sperm and whether Hsp90 in sperm is palmitoylated under different physiological conditions. In this study, we examined whether the protein palmitoylation is present in mouse cauda epididymis sperm using acyl-biotin exchange method, predicted the potential palmitoylated sites of Hsp90 by the software CSS-Palm 4.0 and detected the palmitoylated Hsp90 in the mouse sperm from caput epididymis and cauda epididymis by immunoprecipitation. We found that some proteins, approximately 50, 65, 72, 85 and 130 kDa, were palmitoylated in mouse cauda epididymis sperm. Five sites in two Hsp90 isoforms were predicted to be palmitoylated. The results also showed that Hsp90 in mouse sperm was palmitoylated and its palmitoylation level was involved in different physiological conditions: the palmitoylation level of cauda epididymis sperm was higher than that of caput epididymis sperm; and the palmitoylation level after capacitation was much higher than that before capacitation. In conclusion, this study reveals that protein palmitoylation is present in mouse sperm and the palmitoylated Hsp90 is associated with different physiological conditions in sperm.

Key words: Sperm; protein palmitoylation; acyl-biotin exchange method; heat shock protein 90

收稿日期:2017-01-14  录用日期:2017-04-06

通讯作者:倪崖  E-mail: niya99@126.com

引用本文:

李瑞, 李坤, 杨岳, 孙培蓓, 陈爱君, 倪崖. 小鼠精子热休克蛋白90的棕榈酰化[J]. 生理学报 2017; 69 (3): 298-304.

LI Rui, LI Kun, YANG Yue, SUN Pei-Bei, CHEN Ai-Jun, NI Ya. [Palmitoylation of heat shock protein 90 in mouse sperm.] [Article in Chinese]. Acta Physiol Sin 2017; 69 (3): 298-304 (in Chinese with English abstract).