Suppr超能文献

一种用于成像蛋白质胞吐作用的荧光化学遗传pH传感器。

A Fluorogenic Chemogenetic pH Sensor for Imaging Protein Exocytosis.

作者信息

Coïs Justine, Niepon Marie-Laure, Wittwer Manon, Sepasi Tehrani Hessam, Bun Philippe, Mallet Jean-Maurice, Vialou Vincent, Dumat Blaise

机构信息

Laboratoire des biomolécules, LBM, Département de chimie, École normale supérieure, PSL University, Sorbonne Université, CNRS, 75005 Paris, France.

Laboratoire Neurosciences Paris Seine, Sorbonne Université, CNRS, INSERM, Paris 75005, France.

出版信息

ACS Sens. 2024 Sep 27;9(9):4690-4700. doi: 10.1021/acssensors.4c01057. Epub 2024 Aug 15.

Abstract

Fluorescent protein-based pH biosensors enable the tracking of pH changes during protein trafficking and, in particular, exocytosis. The recent development of chemogenetic reporters combining synthetic fluorophores with self-labeling protein tags offers a versatile alternative to fluorescent proteins that combines the diversity of chemical probes and indicators with the selectivity of the genetic encoding. However, this hybrid protein labeling strategy does not avoid common drawbacks of organic fluorophores such as the risk of off-target signal due to unbound molecules. Here, we describe a novel fluorogenic and chemogenetic pH sensor based on a cell-permeable molecular pH indicator called , whose fluorescence can be locally activated in cells by reaction with HaloTag, ensuring excellent signal selectivity in wash-free imaging experiments. was selected out of a series of four fluorogenic molecular rotor structures based on protein chromophore analogues. It displays good pH sensitivity with a p of 6.3 well-suited to monitor pH variations during exocytosis and an excellent labeling selectivity in cells. It was applied to follow the secretion of CD63-HaloTag fusion proteins using TIRF microscopy. We anticipate that this strategy based on the combination of a tunable and chemically accessible fluorogenic probe with a well-established protein tag will open new possibilities for the development of versatile alternatives to fluorescent proteins for elucidating the dynamics and regulatory mechanisms of proteins in living cells.

摘要

基于荧光蛋白的pH生物传感器能够追踪蛋白质运输过程中的pH变化,尤其是胞吐作用期间的pH变化。近期,将合成荧光团与自标记蛋白标签相结合的化学遗传报告分子的发展,为荧光蛋白提供了一种通用的替代方案,该方案将化学探针和指示剂的多样性与遗传编码的选择性结合在一起。然而,这种杂交蛋白标记策略并不能避免有机荧光团的常见缺点,比如未结合分子导致的脱靶信号风险。在此,我们描述了一种基于一种名为的可穿透细胞的分子pH指示剂的新型荧光和化学遗传pH传感器,其荧光可通过与HaloTag反应在细胞内局部激活,从而在免洗成像实验中确保出色的信号选择性。是从基于蛋白质发色团类似物的一系列四种荧光分子转子结构中筛选出来的。它具有良好的pH敏感性,pKa为6.3,非常适合监测胞吐作用期间的pH变化,并且在细胞中具有出色的标记选择性。它被应用于使用全内反射荧光显微镜(TIRF显微镜)追踪CD63-HaloTag融合蛋白的分泌。我们预计,这种基于可调谐且化学上可及的荧光探针与成熟的蛋白标签相结合的策略,将为开发用于阐明活细胞中蛋白质动力学和调控机制的荧光蛋白通用替代方案开辟新的可能性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验