用于评估蛋白激酶A活性的激酶迁移转移试验(KiMSA)。

IF 1 Q3 BIOLOGY
Analia G Novero, Tomás J Steeman, Catalina Curcio, Lara Buccolini, Andres Binolfi, Diego Krapf, Mariano G Buffone, Dario Krapf, Cintia Stival
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引用次数: 0

摘要

camp依赖性蛋白激酶(PKA)是细胞内信号级联中分布最广泛的激酶之一,在包括精子细胞获能在内的各种过程的调控中起着关键作用。传统的PKA活性评估依赖于[γ-32P] ATP和Kemptide肽作为底物的利用。这一战略有几个主要缺点,包括成本高和操纵放射性同位素带来的健康风险。在这项工作中,我们引入了一种增强的非放射性分析来量化PKA活性,称为激酶迁移量转移分析(KiMSA),基于使用荧光标记的Kemptide (Kemptide- fitc)。一旦激酶反应终止,产物可以很容易地通过琼脂糖凝胶电泳和荧光密度测定法进行分辨。我们发现KiMSA既适用于分离的PKA,也适用于细胞提取物中的酶。此外,它还可以量化小鼠精子获能过程中的PKA活性。此外,该检测还可以监测活细胞中药理学抑制剂对PKA的抑制作用。因此,设置实验和最佳分析条件,以便KiMSA可以用于评估精子细胞中体外和体内PKA活性。最后,这种方法可以测量cAMP浓度,为cAMP/PKA途径的研究提供了一种通用的技术。•KiMSA是一种多功能激酶迁移转移测定法,用于测量精子生理中的PKA活性,用荧光标记的底物代替放射性测定法,具有高灵敏度。•这种体外检测能够评估纯化或突变后的激活状态、药物效应或PKA动力学。•该试验测量来自细胞提取物的PKA活性,反映裂解前激活状态和细胞内信号传导,尽管不是真实的体内读数。•标准方案完成时间为一天,包括精子准备,激酶反应,电泳和荧光定量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Kinase Mobility Shift Assay (KiMSA) for Assessing Protein Kinase A Activity.

The cAMP-dependent protein kinase (PKA) is one of the most extensively distributed kinases among intracellular signal cascades, with a pivotal role in the regulation of various processes, including the capacitation of sperm cells. Traditional assessments of PKA activity rely on the utilization of [γ-32P] ATP and the Kemptide peptide as a substrate. This strategy presents several major drawbacks, including high costs and health risks derived from the manipulation of radioactive isotopes. In this work, we introduce an enhanced non-radioactive assay to quantify PKA activity, termed kinase mobility shift assay (KiMSA), based on the use of a fluorescent-labeled Kemptide (Kemptide-FITC). Once the kinase reaction is terminated, the products can be easily resolved through electrophoresis on an agarose gel and quantified by fluorescence densitometry. We show that KiMSA is suitable for isolated PKA as well as for the enzyme in cell extracts. In addition, it enables quantification of PKA activity during the progression of mouse sperm capacitation. Furthermore, the assay enables monitoring the inhibition of PKA with pharmacological inhibitors in live cells. Therefore, the experimental and optimal assay conditions are set so that KiMSA can be used to assess in vitro as well as in vivo PKA activity in sperm cells. Finally, this method allows for measurement of cAMP concentrations, rendering a versatile technique for the study of cAMP/PKA pathways. Key features • KiMSA is a versatile kinase mobility shift assay for measuring PKA activity in sperm physiology, replacing radioactive assays with a fluorescence-labeled substrate for high sensitivity. • This in vitro assay enables evaluation of activation state, drug effects, or PKA kinetics after purification or mutation. • This assay measures PKA activity from cell extracts, reflecting pre-lysis activation status and intracellular signaling, though not a true in vivo readout. • The standard protocol completion time is one day, including sperm preparation, kinase reactions, electrophoresis, and fluorescence quantification.

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