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用于研究L-乳酸生物学作用的光笼型L-乳酸的合成与应用。

Synthesis and application of a photocaged-L-lactate for studying the biological roles of L-lactate.

作者信息

Miyazaki Ikumi, Tsao Kelvin K, Kamijo Yuki, Nasu Yusuke, Terai Takuya, Campbell Robert E

机构信息

Department of Chemistry, Graduate School of Science, The University of Tokyo, Bunkyo-ku, Tokyo, Japan.

Global Standard Science Education Division, Graduate School of Science, The University of Tokyo, Bunkyo-ku, Tokyo, Japan.

出版信息

Commun Chem. 2025 Apr 5;8(1):104. doi: 10.1038/s42004-025-01495-1.

Abstract

L-Lactate, once considered a metabolic waste product of glycolysis, is now recognized as a vitally important metabolite and signaling molecule in multiple biological pathways. However, exploring L-lactate's emerging intra- and extra-cellular roles is hindered by a lack of tools to perturb L-lactate concentration intracellularly and extracellularly. Photocaged compounds are a powerful way to introduce bioactive molecules with spatiotemporal precision using illumination. Here, we report the development of a photocaged derivative of L-lactate, 4-methoxy-7-nitroindolinyl-L-lactate (MNI-L-lac), that releases L-lactate upon illumination. We validated MNI-L-lac in cell culture by demonstrating that the photorelease of L-lactate elicits a response from genetically encoded extra- and intracellular L-lactate biosensors (eLACCO1, eLACCO2.1, R-iLACCO1.2). To demonstrate the utility of MNI-L-lac, we employed the photorelease of L-lactate to activate G protein-coupled receptor 81 (GPR81), as revealed by the inhibition of adenylyl cyclase activity and concomitant decrease of cAMP. These results indicate that MNI-L-lac may be useful for perturbing the concentration of endogenous L-lactate in order to investigate L-lactate's roles in metabolic and signaling pathways.

摘要

L-乳酸,曾被认为是糖酵解的代谢废物,如今被公认为多种生物途径中至关重要的代谢物和信号分子。然而,由于缺乏在细胞内和细胞外扰动L-乳酸浓度的工具,探索L-乳酸新出现的细胞内和细胞外作用受到了阻碍。光笼化合物是一种利用光照以时空精确性引入生物活性分子的有效方法。在此,我们报告了一种L-乳酸的光笼衍生物,4-甲氧基-7-硝基吲哚啉基-L-乳酸(MNI-L-lac)的开发,其在光照下会释放L-乳酸。我们通过证明L-乳酸的光释放引发了基因编码的细胞外和细胞内L-乳酸生物传感器(eLACCO1、eLACCO2.1、R-iLACCO1.2)的反应,在细胞培养中验证了MNI-L-lac。为了证明MNI-L-lac的实用性,我们利用L-乳酸的光释放来激活G蛋白偶联受体81(GPR81),这通过腺苷酸环化酶活性的抑制和cAMP的相应减少得以揭示。这些结果表明,MNI-L-lac可能有助于扰动内源性L-乳酸的浓度,以便研究L-乳酸在代谢和信号通路中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/effb/11972357/c3abdf6e6b5a/42004_2025_1495_Fig1_HTML.jpg

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