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基于荧光的 Xenopus laevis 卵母细胞中膜结合的血管紧张素转换酶 2 活性的测量。

Fluorescence-Based Measurements of Membrane-Bound Angiotensin Converting Enzyme 2 Activity Using Xenopus Laevis Oocytes.

机构信息

Department of Evolutionary Genetics, Max Planck Institute for Evolutionary Anthropology, 04103 Leipzig, Germany.

Department of Neuroscience, Karolinska Institutet, 17177 Stockholm, Sweden.

出版信息

Biosensors (Basel). 2022 Aug 4;12(8):601. doi: 10.3390/bios12080601.

Abstract

Functional investigations of enzymes involving cellular expression systems are important for pharmacological studies. The precise control of expression is challenging in transiently transfected mammalian cell lines. Here, we explored the ability of Xenopus laevis oocytes to express a membrane-bound enzyme for functional characterization using standard 96-well plates and a fluorescence-based plate reader assay. We microinjected oocytes with cRNA encoding the angiotensin converting enzyme 2 (ACE2) and measured the enzymatic activity in single oocytes using a commercial fluorescence-based assay. The injected oocytes showed up to a 50-fold increase in fluorescence compared to uninjected oocytes. This fluorescence intensity was dose-dependent on the amount of cRNA. These results suggest that Xenopus oocytes can be used for the functional evaluation of membrane-bound enzymes, decreasing the experimental workload.

摘要

研究涉及细胞表达系统的酶的功能对于药理学研究非常重要。在瞬时转染的哺乳动物细胞系中,精确控制表达是具有挑战性的。在这里,我们探索了非洲爪蟾卵母细胞表达一种膜结合酶的能力,以便使用标准的 96 孔板和基于荧光的板读数测定法进行功能表征。我们将编码血管紧张素转换酶 2(ACE2)的 cRNA 微注射到卵母细胞中,并使用商业的基于荧光的测定法在单个卵母细胞中测量酶活性。与未注射的卵母细胞相比,注射的卵母细胞的荧光强度增加了多达 50 倍。这种荧光强度与 cRNA 的量呈剂量依赖性。这些结果表明,非洲爪蟾卵母细胞可用于膜结合酶的功能评估,从而减少实验工作量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a48b/9405939/21598c2b5305/biosensors-12-00601-g001.jpg

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