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蛋白质组学方法与酒精中毒新治疗靶点的鉴定

Proteomic approaches and identification of novel therapeutic targets for alcoholism.

作者信息

Gorini Giorgio, Harris R Adron, Mayfield R Dayne

机构信息

Waggoner Center for Alcohol and Addiction Research, The University of Texas at Austin, Austin, TX, USA.

出版信息

Neuropsychopharmacology. 2014 Jan;39(1):104-30. doi: 10.1038/npp.2013.182. Epub 2013 Jul 31.

Abstract

Recent studies have shown that gene regulation is far more complex than previously believed and does not completely explain changes at the protein level. Therefore, the direct study of the proteome, considerably different in both complexity and dynamicity to the genome/transcriptome, has provided unique insights to an increasing number of researchers. During the past decade, extraordinary advances in proteomic techniques have changed the way we can analyze the composition, regulation, and function of protein complexes and pathways underlying altered neurobiological conditions. When combined with complementary approaches, these advances provide the contextual information for decoding large data sets into meaningful biologically adaptive processes. Neuroproteomics offers potential breakthroughs in the field of alcohol research by leading to a deeper understanding of how alcohol globally affects protein structure, function, interactions, and networks. The wealth of information gained from these advances can help pinpoint relevant biomarkers for early diagnosis and improved prognosis of alcoholism and identify future pharmacological targets for the treatment of this addiction.

摘要

最近的研究表明,基因调控比之前认为的要复杂得多,并且不能完全解释蛋白质水平的变化。因此,对蛋白质组的直接研究,其在复杂性和动态性方面与基因组/转录组有很大不同,为越来越多的研究人员提供了独特的见解。在过去十年中,蛋白质组学技术取得了非凡进展,改变了我们分析神经生物学条件改变背后蛋白质复合物和信号通路的组成、调控及功能的方式。当与互补方法相结合时,这些进展为将大数据集解码为有意义的生物适应性过程提供了背景信息。神经蛋白质组学通过使人们更深入地了解酒精如何全面影响蛋白质结构、功能、相互作用和网络,为酒精研究领域带来了潜在突破。从这些进展中获得的丰富信息有助于确定酒精中毒早期诊断和改善预后的相关生物标志物,并识别未来治疗这种成瘾性疾病的药理学靶点。

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