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利用荧光凝胶迁移电泳快速检测小鼠精子中的糖原合酶激酶-3活性

Rapid Detection of Glycogen Synthase Kinase-3 Activity in Mouse Sperm Using Fluorescent Gel Shift Electrophoresis.

作者信息

Choi Hoseok, Choi Bomi, Seo Ju Tae, Lee Kyung Jin, Gye Myung Chan, Kim Young-Pil

机构信息

Department of Life Science, Hanyang University, Seoul 04763, Korea.

Research Institute for Natural Sciences, Hanyang University, Seoul 04763, Korea.

出版信息

Sensors (Basel). 2016 Apr 16;16(4):551. doi: 10.3390/s16040551.

Abstract

Assaying the glycogen synthase kinase-3 (GSK3) activity in sperm is of great importance because it is closely implicated in sperm motility and male infertility. While a number of studies on GSK3 activity have relied on labor-intensive immunoblotting to identify phosphorylated GSK3, here we report the simple and rapid detection of GSK3 activity in mouse sperm using conventional agarose gel electrophoresis and a fluorescent peptide substrate. When a dye-tethered and prephosphorylated (primed) peptide substrate for GSK3 was employed, a distinct mobility shift in the fluorescent bands on the agarose was observed by GSK3-induced phosphorylation of the primed peptides. The GSK3 activity in mouse testes and sperm were quantifiable by gel shift assay with low sample consumption and were significantly correlated with the expression levels of GSK3 and p-GSK3. We suggest that our assay can be used for reliable and rapid detection of GSK3 activity in cells and tissue extracts.

摘要

检测精子中的糖原合酶激酶-3(GSK3)活性非常重要,因为它与精子活力和男性不育密切相关。虽然许多关于GSK3活性的研究依赖于劳动强度大的免疫印迹法来鉴定磷酸化的GSK3,但在此我们报告使用传统琼脂糖凝胶电泳和荧光肽底物对小鼠精子中的GSK3活性进行简单快速的检测。当使用与染料相连且预磷酸化(引发)的GSK3肽底物时,通过引发肽的GSK3诱导磷酸化,在琼脂糖上的荧光带中观察到明显的迁移率变化。通过凝胶迁移分析可对小鼠睾丸和精子中的GSK3活性进行定量,样品消耗量低,且与GSK3和p-GSK3的表达水平显著相关。我们认为我们的检测方法可用于可靠且快速地检测细胞和组织提取物中的GSK3活性。

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