Putative Retina Metal/Metalloid-Binding Proteins: Molecular Functions, Biological Processes and Retina Disease Associations.

IF 2.9 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Metallomics Pub Date : 2024-09-25 DOI:10.1093/mtomcs/mfae045
Marta Ugarte, Craig Lawless
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引用次数: 0

Abstract

Background: The mammalian retina contains high amounts of metals/metalloid-selenium. Their dyshomeostases are associated with certain retinal diseases. We carried out this bioinformatics study to identify the relationships between putative retinal metal/selenium binding proteins, their molecular functions and biological processes.

Methods: Identification of putative mouse metal/selenium binding proteins was based on known binding motifs, domains, patterns, and profiles. Annotations were obtained from Uniprot keyword "metal binding", "metal ion co-factors", "selenium proteins". Protein functions were estimated by associative frequency with key words in UniProt annotations. The raw data of 5 mouse proteomics PRIDE datasets (available to date) were downloaded and processed with Mascot against the mouse taxa of Uniprot (SwissProt/Trembl) and MaxQuant (version 1.6.10.43) for qualitative and quantitative datasets, respectively. Clinically relevant variants were evaluated using archive and aggregates information in ClinVar.

Results: The 438 proteins common to all the retina proteomics datasets were used to identify over-represented Gene Ontology categories. The putative mouse retinal metal/metalloid binding proteins identified are mainly involved in: 1) metabolic processes (enzymes), 2) homeostasis, 3) transport (vesicle mediated, transmembrane, along microtubules), 4) cellular localisation, 5) regulation of signalling and exocytosis, 6) organelle organisation, 7) (de)phosphorylation and 8) complex assembly. Twenty-one proteins were identified as involved in response to light stimulus and/or visual system development. An association of metal ion binding proteins rhodopsin, photoreceptor specific nuclear receptor, calcium binding protein 4 with disease-related mutations in inherited retinal conditions was identified, where the mutations affected an area within or in close proximity to the metal binding site or domain.

Conclusion: These findings suggest a functional role for the putative metal/metalloid binding site in retinal proteins in certain retinal disorders.

视网膜金属/类金属结合蛋白:分子功能、生物过程和视网膜疾病相关性。
背景:哺乳动物视网膜含有大量金属/类金属硒。它们的失调与某些视网膜疾病有关。我们开展了这项生物信息学研究,以确定推定视网膜金属/硒结合蛋白、其分子功能和生物过程之间的关系:方法:根据已知的结合基元、结构域、模式和轮廓鉴定推定的小鼠金属/硒结合蛋白。注释来自 Uniprot 关键字 "金属结合"、"金属离子辅助因子 "和 "硒蛋白"。蛋白质功能是通过与 UniProt 注释中关键词的关联频率来估算的。下载了 5 个小鼠蛋白质组学 PRIDE 数据集(迄今已有)的原始数据,并使用 Mascot 对 Uniprot(SwissProt/Trembl)和 MaxQuant(1.6.10.43 版)的小鼠分类群分别进行了定性和定量数据集处理。利用 ClinVar.Results 中的档案和聚合信息对临床相关变异进行了评估:结果:所有视网膜蛋白质组学数据集共有的 438 个蛋白质被用来识别代表性过高的基因本体类别。鉴定出的推定小鼠视网膜金属/类金属结合蛋白主要涉及以下方面1)代谢过程(酶);2)平衡;3)运输(囊泡介导的、跨膜的、沿微管的);4)细胞定位;5)信号传导和外泌调节;6)细胞器组织;7)(去)磷酸化;8)复合物组装。鉴定出 21 个蛋白质参与了对光刺激的反应和/或视觉系统的发育。在遗传性视网膜疾病中,发现金属离子结合蛋白视网膜蛋白、感光器特异性核受体、钙结合蛋白4与疾病相关的突变有关联,这些突变影响金属结合位点或结构域内的一个区域或靠近该区域的区域:这些发现表明,视网膜蛋白中的假定金属/类金属结合位点在某些视网膜疾病中具有功能性作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Metallomics
Metallomics 生物-生化与分子生物学
CiteScore
7.00
自引率
5.90%
发文量
87
审稿时长
1 months
期刊介绍: Global approaches to metals in the biosciences
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