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基于荧光素酶的分裂测定法,使用 hiPSC 衍生的运动神经元检测肉毒神经毒素。

Split luciferase-based assay to detect botulinum neurotoxins using hiPSC-derived motor neurons.

机构信息

IPSEN Innovation, 5 avenue du Canada, 91940, Les Ulis, France.

Department of Urology, Boston Children's Hospital, Boston, MA, 02115, USA.

出版信息

Commun Biol. 2023 Jan 30;6(1):122. doi: 10.1038/s42003-023-04495-w.

Abstract

Botulinum neurotoxins (BoNTs) have been widely used clinically as a muscle relaxant. These toxins target motor neurons and cleave proteins essential for neurotransmitter release like Synaptosomal-associated protein of 25 kDa (SNAP-25). In vitro assays for BoNT testing using rodent cells or immortalized cell lines showed limitations in accuracy and physiological relevance. Here, we report a cell-based assay for detecting SNAP-25-cleaving BoNTs by combining human induced Pluripotent Stem Cells (hiPSC)-derived motor neurons and a luminescent detection system based on split NanoLuc luciferase. This assay is convenient, rapid, free-of-specialized antibodies, with a detection sensitivity of femtomolar concentrations of toxin, and can be used to study the different steps of BoNT intoxication.

摘要

肉毒神经毒素(BoNTs)已被广泛临床应用为肌肉松弛剂。这些毒素以运动神经元为靶点,切割神经递质释放所必需的蛋白质,如突触相关蛋白 25kDa(SNAP-25)。使用啮齿动物细胞或永生化细胞系进行 BoNT 检测的体外测定在准确性和生理相关性方面存在局限性。在这里,我们通过结合人诱导多能干细胞(hiPSC)衍生的运动神经元和基于分裂 NanoLuc 荧光素酶的发光检测系统,报告了一种用于检测切割 SNAP-25 的 BoNTs 的基于细胞的测定法。该测定法方便、快速、无需专用抗体,对毒素的检测灵敏度达到飞摩尔浓度,可用于研究 BoNT 中毒的不同步骤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76a6/9886929/c85b117366db/42003_2023_4495_Fig1_HTML.jpg

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