利用序列挖掘技术鉴定糖尿病视网膜病变的蛋白质生物标志物

Ratnagiri Devarapu, G. Murali, H. Thota
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引用次数: 1

摘要

生物信息学和序列挖掘是数据挖掘技术的应用和发展,通过理解生物数据来解决问题。序列分析是序列挖掘技术中最原始的操作。现代序列挖掘研究专门分析相互关联和不同的序列模式,并利用检索到的序列来分析不同蛋白质序列之间的相似性和距离。糖尿病视网膜病变是导致大多数成年糖尿病患者失明的主要原因,也是世界各地糖尿病的常见问题。各种研究分析表明,有许多蛋白质被发现参与糖尿病视网膜病变。在本文中,我们利用多重比对工具Clustal Omega对某些与糖尿病视网膜病变密切相关的蛋白质进行了评估,并获得了从国家生物技术信息中心(NCBI)收集的28个蛋白质序列的系统发育树。在这项工作中,称为序列挖掘的数据挖掘技术在提供通过邻居连接算法获得的系统图方面发挥着重要作用。从系统发育树上可以看出,皮质醇抑制素、维生素D受体和生长抑素蛋白与糖尿病视网膜病变密切相关。还进行了分子对接研究,这是计算蛋白质-配体相互作用最广泛使用的方法。在计算机对接研究中表明,四种抑制性化合物,即槲皮素、山奈酚、纳林宁和Melicitrin,与醛糖还原酶相互作用,醛糖还原酶也被发现在糖尿病视网膜病变中发挥作用。结果表明,旨在标准化皮质醇抑制素、维生素D受体和生长抑素活性的技术在抑制糖尿病视网膜病变方面具有巨大优势和益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of Protein Biomarkers for Diabetic Retinopathy using Sequence Mining Techniques
Bioinformatics and sequence mining are the application and development of data mining techniques to solve problems by comprehending biological data. Sequence analysis is the most primitive operation in sequence mining techniques. Modern sequence mining research is specialized in analyzing sequential patterns which are relevant and distinct from one another and utilizing retrieved sequences similarity and distance between different protein sequences can be analyzed. Diabetic retinopathy is the major cause of blindness in individuals mostly adults with diabetes and is it is the common problem of diabetes mellitus across the world. Various research analyses stated that there are many proteins which are found to take part in diabetic retinopathy. In this paper, we have evaluated certain proteins which are closely related with diabetic retinopathy with the help of multiple alignment tool viz. Clustal Omega and obtained a phylogenetic tree of 28 protein sequences gathered from National Center for Biotechnology Information (NCBI). In this work data mining technique called sequence mining plays a significant role in providing phylogram obtained with Neighbor-Joining algorithm. From the phylogenetic tree it was recognized that cortistatin, vitamin-D receptor and somatostatin proteins has close connection with diabetic retinopathy. Molecular docking studies have also been performed which is the most extensively used method for the calculation of protein-ligand interactions. In silico docking studies indicated that four inhibitory compounds i.e. Quercetin, Kaempferol, Naringenin and Melicitrin interact with aldose reductase which also found to have role in diabetic retinopathy. Outcomes infer that techniques intended to standardize cortistatin, vitamin-D receptor and somatostatin activities be of huge advantage and provide benefit in inhibiting diabetic retinopathy.
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