研究荧光探针与锥虫- trna合成酶的结合:荧光光谱和分子动力学研究。

IF 3.8 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Archives of biochemistry and biophysics Pub Date : 2025-02-01 DOI:10.1016/j.abb.2024.110263
Pratyasha Bhowal , David Jameson , Rajat Banerjee
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引用次数: 0

摘要

鉴于美洲恰加斯病的高流行率,我们针对其病原体克氏锥虫独特的精氨酸- trna合成酶。在其许多可能的用途中,萘衍生的荧光配体,如ANS和双ANS,可用于药代动力学研究。尽管ANS和bis-ANS已经成为蛋白质表征的重要荧光探针,但蛋白质-ANS/bis-ANS复合物的结构和光谱特征在很大程度上仍然未知。两种荧光染料都与蛋白质的折叠或部分折叠的疏水区域结合。此外,它们还用于识别熔融的球状中间物。这些探针已被用于研究蛋白质结构的折叠问题和蛋白质-蛋白质相互作用的机制。在与TcArgRS结合后,ANS和bis-ANS的发射光谱明显增强和蓝移,TcArgRS是负责将l -精氨酸附着到相应tRNA上的主要酶。通过荧光光谱和计算研究,我们得出bis-ANS与TcArgRS结合更紧密,ATP影响了bis-ANS的荧光信号。因此,这些探针是研究蛋白质在结构、功能和机制方面复杂的分子间关系的有用资源。我们的研究为识别TcArgRS中存在的疏水区域提供了一个框架。疏水贴片在蛋白质上用于药物靶向是值得注意的,因为它们可以帮助识别蛋白质表面可能与配体相互作用的区域。这些补丁有助于识别在确定结合亲和力中起重要作用的热点残基。药物本质上主要是小而疏水的,它们靶向具有互补性质的蛋白质表面。在这项研究中,我们阐明了TcArgRS作为对抗锥虫病和延长预期寿命的靶点的潜力。
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Investigating the binding of fluorescent probes to a trypanosomal-tRNA synthetase: A fluorescence spectroscopic and molecular dynamics study
Given the high prevalence of Chagas disease in the Americas, we targeted the unique arginyl-tRNA synthetase of its causative agent Trypanosoma cruzi. Among their many possible uses, naphthalene-derived fluorescent ligands, such as ANS and bis-ANS, may be employed in pharmacokinetic research. Although ANS and bis-ANS have become prominent fluorescent probes for protein characterization, the structural and spectroscopic characteristics of protein-ANS/bis-ANS complexes remain largely unknown. Both fluorescent dyes bind to either the folded or partially folded hydrophobic regions of proteins. Additionally, they serve to identify molten globule-like intermediates. These probes have been used to study the folding problems of protein structures and the mechanisms of protein-protein interactions. ANS and bis-ANS exhibited significant enhancement and blue shift in their emission spectra upon binding to TcArgRS, the primary enzyme responsible for attaching l-arginine to its corresponding tRNA. Through fluorescence spectroscopy and computational studies, we concluded that bis-ANS binds more tightly to TcArgRS and that ATP affects bis-ANS fluorescence signal. Thus, these probes are useful resources for studying the intricate intermolecular relationships between proteins in terms of their structure, function, and mechanism. Our study provides a framework for identifying the hydrophobic regions present in TcArgRS. The utilization of hydrophobic patches on proteins for drug targeting is noteworthy because they can assist in identifying regions on the surface of proteins that are likely to interact with ligands. These patches help identify hotspot residues that play a vital role in determining binding affinity. Drugs are mainly small and hydrophobic in nature, and they target protein surfaces which have complementary properties. In this study, we elucidated the potential of TcArgRS as a target for combating trypanosomal diseases and extending life expectancy.
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来源期刊
Archives of biochemistry and biophysics
Archives of biochemistry and biophysics 生物-生化与分子生物学
CiteScore
7.40
自引率
0.00%
发文量
245
审稿时长
26 days
期刊介绍: Archives of Biochemistry and Biophysics publishes quality original articles and reviews in the developing areas of biochemistry and biophysics. Research Areas Include: • Enzyme and protein structure, function, regulation. Folding, turnover, and post-translational processing • Biological oxidations, free radical reactions, redox signaling, oxygenases, P450 reactions • Signal transduction, receptors, membrane transport, intracellular signals. Cellular and integrated metabolism.
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