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使用iTRAQ技术鉴定房水中与白内障形成相关的蛋白质。

Identification of proteins in the aqueous humor associated with cataract development using iTRAQ methodology.

作者信息

Xiang Minhong, Zhang Xingru, Li Qingsong, Wang Hanmin, Zhang Zhenyong, Han Zhumei, Ke Meiqing, Chen Xingxing

机构信息

Department of Ophthalmology, Putuo Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai 200062, P.R. China.

出版信息

Mol Med Rep. 2017 May;15(5):3111-3120. doi: 10.3892/mmr.2017.6345. Epub 2017 Mar 21.

Abstract

Proteins in the aqueous humor (AH) are important in the induction of cataract development. The identification of cataract-associated proteins assists in identifying patients and predisposed to the condition and improve treatment efficacy. Proteomics analysis has previously been used for identifying protein markers associated with eye diseases; however, few studies have examined the proteomic alterations in cataract development due to high myopia, glaucoma and diabetes. The present study, using the isobaric tagging for relative and absolute protein quantification methodology, aimed to examine cataract-associated proteins in the AH from patients with high myopia, glaucoma or diabetes, and controls. The results revealed that 445 proteins were identified in the AH groups, compared with the control groups, and 146, 264 and 130 proteins were differentially expressed in the three groups of patients, respectively. In addition, 44 of these proteins were determined to be cataract‑associated, and the alterations of five randomly selected proteins were confirmed using enzyme-linked immunosorbent assays. The biological functions of these 44 cataract-associated proteins were analyzed using Gen Ontology/pathways annotation, in addition to protein‑protein interaction network analysis. The results aimed to expand current knowledge of the pathophysiologic characteristics of cataract development and provided a panel of candidates for biomarkers of the disease, which may assist in further diagnosis and the monitoring of cataract development.

摘要

房水中的蛋白质在白内障形成过程中起着重要作用。鉴定与白内障相关的蛋白质有助于识别易患该疾病的患者,并提高治疗效果。蛋白质组学分析此前已被用于识别与眼部疾病相关的蛋白质标志物;然而,很少有研究探讨高度近视、青光眼和糖尿病导致的白内障发展过程中的蛋白质组学变化。本研究采用相对和绝对蛋白质定量的等压标记方法,旨在检测高度近视、青光眼或糖尿病患者及对照组房水中与白内障相关的蛋白质。结果显示,与对照组相比,房水组共鉴定出445种蛋白质,三组患者分别有146、264和130种蛋白质差异表达。此外,确定其中44种蛋白质与白内障相关,并通过酶联免疫吸附试验证实了随机选择的5种蛋白质的变化。除蛋白质-蛋白质相互作用网络分析外,还使用基因本体论/通路注释分析了这44种与白内障相关蛋白质的生物学功能。这些结果旨在扩展目前对白内障发展病理生理特征的认识,并提供一组疾病生物标志物候选物,这可能有助于进一步诊断和监测白内障的发展。

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