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分析神经炎症细胞中的半胱氨酸蛋白酶活性。

Profiling Cysteine Proteases Activities in Neuroinflammatory Cells.

作者信息

Agost-Beltrán Laura, Canseco-Rodríguez Ania, Schirmeister Tanja, Rodríguez Santiago, Sánchez-Pérez Ana María, González Florenci V

机构信息

Departament de Química Inorgànica i Orgànica, Universitat Jaume I, Castelló de la Plana, 12071, Spain.

Neurobiotecnologia, Institute of advanced materials (INAM), Universitat Jaume I, Castelló de la Plana, 12071, Spain.

出版信息

ChemMedChem. 2025 Feb 1;20(3):e202400520. doi: 10.1002/cmdc.202400520. Epub 2024 Nov 20.

DOI:10.1002/cmdc.202400520
PMID:39475209
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11793851/
Abstract

A new activity-based probe (ABP) of cysteine proteases (FGA139) has been designed and synthesized. The design of the ABP has been done based upon the chemical structure of an irreversible inhibitor of cysteine proteases by attaching a bodipy fluorophore at the N-terminus of the peptide backbone. The synthetic route of the probe has a metathesis and a "click" reaction as key steps. Although some studies have been reported about the role played by cysteine proteases in neurodegenerative diseases, there are not definitive conclusions. The obtained ABP has been employed as a chemical tool to profile activities of cysteine proteases cathepsins B, L, and calpain in neurodegenerative cell models through confocal imaging. Colocalization of the probe to specific antibodies of the proteases and competitive experiments with non-fluorescent inhibitors confirm the specificity of the ABP. From a theranostic perspective, our findings strongly suggest that FGA139 exhibits a protective role in various cell lines against oxidative stress or pro-inflammatory toxicity and it effectively attenuates macrophage activation triggered by LPS.

摘要

一种新型的基于活性的半胱氨酸蛋白酶探针(ABP,FGA139)已被设计并合成。该ABP的设计基于半胱氨酸蛋白酶不可逆抑制剂的化学结构,通过在肽主链的N端连接一个硼二吡咯荧光团来实现。该探针的合成路线以复分解反应和“点击”反应为关键步骤。尽管已经有一些关于半胱氨酸蛋白酶在神经退行性疾病中作用的研究报道,但尚无定论。所获得的ABP已被用作一种化学工具,通过共聚焦成像来分析神经退行性细胞模型中半胱氨酸蛋白酶组织蛋白酶B、L和钙蛋白酶的活性。探针与蛋白酶特异性抗体的共定位以及与非荧光抑制剂的竞争性实验证实了ABP的特异性。从治疗诊断的角度来看,我们的研究结果强烈表明,FGA139在各种细胞系中对氧化应激或促炎毒性具有保护作用,并且它能有效减弱由脂多糖触发的巨噬细胞激活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4d8/11793851/5d7d013ad439/CMDC-20-e202400520-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4d8/11793851/3cdcfdd9f9e2/CMDC-20-e202400520-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4d8/11793851/dcc4733f99fc/CMDC-20-e202400520-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4d8/11793851/7d8d7f4677c0/CMDC-20-e202400520-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4d8/11793851/b70c3b6157c7/CMDC-20-e202400520-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4d8/11793851/906a1153c18e/CMDC-20-e202400520-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4d8/11793851/dfd63f206a05/CMDC-20-e202400520-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4d8/11793851/5d7d013ad439/CMDC-20-e202400520-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4d8/11793851/3cdcfdd9f9e2/CMDC-20-e202400520-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4d8/11793851/dcc4733f99fc/CMDC-20-e202400520-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4d8/11793851/7d8d7f4677c0/CMDC-20-e202400520-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4d8/11793851/b70c3b6157c7/CMDC-20-e202400520-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4d8/11793851/906a1153c18e/CMDC-20-e202400520-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4d8/11793851/dfd63f206a05/CMDC-20-e202400520-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4d8/11793851/5d7d013ad439/CMDC-20-e202400520-g003.jpg

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本文引用的文献

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Impact of the Warhead of Dipeptidyl Keto Michael Acceptors on the Inhibition Mechanism of Cysteine Protease Cathepsin L.二肽基酮迈克尔受体弹头对半胱氨酸蛋白酶组织蛋白酶L抑制机制的影响
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Origin and Early Diversification of the Papain Family of Cysteine Peptidases.半胱氨酸蛋白酶家族的木瓜蛋白酶的起源和早期多样化。
Int J Mol Sci. 2023 Jul 21;24(14):11761. doi: 10.3390/ijms241411761.
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New insights into the genetic etiology of Alzheimer's disease and related dementias.
阿尔茨海默病及相关痴呆症的遗传学病因新见解。
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What We Learned in 25 Years of Interactive Molecular Design Sessions.二十五载交互式分子设计研讨所得
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Elucidating the Dual Mode of Action of Dipeptidyl Enoates in the Inhibition of Rhodesain Cysteine Proteases.阐明二肽基噁唑烷酮类化合物抑制 Rhodesain 半胱氨酸蛋白酶的双重作用模式。
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