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利用基于氯化的机制来解析亚细胞次氯酸。

Leveraging Chlorination-Based Mechanism for Resolving Subcellular Hypochlorous Acid.

作者信息

Tang Fung Kit, Tucker Lawrence, Nadiveedhi Maheshwara Reddy, Hladun Colby, Morse Jared, Ali Mahnoor, Payne Noah, Schmidt Matthias, Leung Kaho

机构信息

Department of Chemistry & Biochemistry, Clarkson University, NY, 13676, United States.

出版信息

bioRxiv. 2024 Aug 23:2024.08.22.609247. doi: 10.1101/2024.08.22.609247.

Abstract

Hypochlorous acid (HOCl) is crucial for pathogen defense, but an imbalance in HOCl levels can lead to tissue damage and inflammation. Existing HOCl indicators employ an oxidation approach, which may not truly reveal the chlorinative stress environment. We designed a suite of indicators with a new chlorination-based mechanism, termed HOClSense dyes, to resolve HOCl in sub-cellular compartments. HOClSense dyes allow the visualization of HOCl with both switch-on and switch-off detection modes with diverse emission colors, as well as a unique redshift in emission. HOClSense features a minimalistic design with impressive sensing performance in terms of HOCl selectivity, and our design also facilitates functionalization through click chemistry for resolving subcellular HOCl. As a proof of concept, we targeted plasma membrane and lysosomes with HOClSense for subcellular HOCl mapping. With utilizing HOClSense, we discovered the STING pathway-induced HOCl production and the abnormal HOCl production in Niemann-Pick diseases. To the best of our knowledge, this is the first chlorination-based HOCl indicator series for resolving subcellular HOCl.

摘要

次氯酸(HOCl)对病原体防御至关重要,但HOCl水平失衡会导致组织损伤和炎症。现有的HOCl指示剂采用氧化方法,可能无法真正揭示氯化应激环境。我们设计了一套基于新的氯化机制的指示剂,称为HOClSense染料,用于在亚细胞区室中解析HOCl。HOClSense染料能够通过开启和关闭检测模式,以多种发射颜色以及独特的发射红移来可视化HOCl。HOClSense具有简约的设计,在HOCl选择性方面具有令人印象深刻的传感性能,并且我们的设计还通过点击化学促进功能化,以解析亚细胞HOCl。作为概念验证,我们将HOClSense靶向质膜和溶酶体进行亚细胞HOCl定位。利用HOClSense,我们发现了STING途径诱导的HOCl产生以及尼曼-匹克病中异常的HOCl产生。据我们所知,这是首个用于解析亚细胞HOCl的基于氯化的HOCl指示剂系列。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/895b/11370599/729b7b5c08f8/nihpp-2024.08.22.609247v1-f0001.jpg

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