靶向TREM2-TYROBP跨膜结合的药物筛选

IF 6 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
M Cobas-Carreño, A Esteban-Martos, L Tomas-Gallardo, I Iribarren, L Gonzalez-Palma, A Rivera-Ramos, J Elena-Guerra, E Alarcon-Martin, R Ruiz, M J Bravo, J L Venero, X Morató, A Ruiz, J L Royo
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引用次数: 0

摘要

TREM2编码一种参与疾病相关小胶质细胞(DAM)表型的小胶质膜受体,其激活需要与TYROBP跨膜相互作用。TREM2突变是阿尔茨海默病(AD)的一个高影响危险因素,这使TREM2成为一个重要的药物靶点。我们提出了一种细菌双杂交(B2H)系统,设计用于高通量筛选TREM2-TYROBP跨膜相互作用的调节剂。在一项初步研究中,对315种fda批准的药物进行了分析,以确定潜在的结合调节剂。我们的管道包括多个过滤步骤,以确保候选的特异性。筛选提出了两种潜在的候选者,最终在人类小胶质细胞系HMC3中进行了测试。用抗trem2单抗刺激后,在候选蛋白存在的情况下计算pSYK/SYK比率。因此,我们发现伐尼克兰,一种戒烟药物,可以被认为是TREM2-TYROBP相互作用的跨膜激动剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Drug screening targeting TREM2-TYROBP transmembrane binding.

TREM2 encodes a microglial membrane receptor involved in the disease-associated microglia (DAM) phenotype whose activation requires the transmembrane interaction with TYROBP. Mutations in TREM2 represent a high-impact risk factor for Alzheimer's disease (AD) which turned TREM2 into a significant drug target. We present a bacterial two-hybrid (B2H) system designed for high-throughput screening of modulators for the TREM2-TYROBP transmembrane interaction. In a pilot study, 315 FDA-approved drugs were analyzed to identify potential binding modifiers. Our pipeline includes multiple filtering steps to ensure candidate specificity. The screening suggested two potential candidates that were finally assayed in the human microglial cell line HMC3. Upon stimulation with anti-TREM2 mAb, pSYK/SYK ratios were calculated in the presence of the candidates. As a result, we found that varenicline, a smoking cessation medication, can be considered as a transmembrane agonist of the TREM2-TYROBP interaction.

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来源期刊
Molecular Medicine
Molecular Medicine 医学-生化与分子生物学
CiteScore
8.60
自引率
0.00%
发文量
137
审稿时长
1 months
期刊介绍: Molecular Medicine is an open access journal that focuses on publishing recent findings related to disease pathogenesis at the molecular or physiological level. These insights can potentially contribute to the development of specific tools for disease diagnosis, treatment, or prevention. The journal considers manuscripts that present material pertinent to the genetic, molecular, or cellular underpinnings of critical physiological or disease processes. Submissions to Molecular Medicine are expected to elucidate the broader implications of the research findings for human disease and medicine in a manner that is accessible to a wide audience.
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