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聚焦结构基因组学:昆士兰大学的结构生物学流程

Focusing in on structural genomics: the University of Queensland structural biology pipeline.

作者信息

Puri Munish, Robin Gautier, Cowieson Nathan, Forwood Jade K, Listwan Pawel, Hu Shu-Hong, Guncar Gregor, Huber Thomas, Kellie Stuart, Hume David A, Kobe Bostjan, Martin Jennifer L

机构信息

Institute for Molecular Bioscience, University of Queensland, Brisbane, Queensland, Australia.

出版信息

Biomol Eng. 2006 Dec;23(6):281-9. doi: 10.1016/j.bioeng.2006.09.002. Epub 2006 Oct 7.

Abstract

The flood of new genomic sequence information together with technological innovations in protein structure determination have led to worldwide structural genomics (SG) initiatives. The goals of SG initiatives are to accelerate the process of protein structure determination, to fill in protein fold space and to provide information about the function of uncharacterized proteins. In the long-term, these outcomes are likely to impact on medical biotechnology and drug discovery, leading to a better understanding of disease as well as the development of new therapeutics. Here we describe the high throughput pipeline established at the University of Queensland in Australia. In this focused pipeline, the targets for structure determination are proteins that are expressed in mouse macrophage cells and that are inferred to have a role in innate immunity. The aim is to characterize the molecular structure and the biochemical and cellular function of these targets by using a parallel processing pipeline. The pipeline is designed to work with tens to hundreds of target gene products and comprises target selection, cloning, expression, purification, crystallization and structure determination. The structures from this pipeline will provide insights into the function of previously uncharacterized macrophage proteins and could lead to the validation of new drug targets for chronic obstructive pulmonary disease and arthritis.

摘要

新的基因组序列信息洪流,再加上蛋白质结构测定方面的技术创新,催生了全球范围内的结构基因组学(SG)计划。SG计划的目标是加速蛋白质结构测定过程,填补蛋白质折叠空间,并提供有关未表征蛋白质功能的信息。从长远来看,这些成果可能会对医学生物技术和药物研发产生影响,从而加深对疾病的理解,并推动新疗法的开发。在此,我们描述澳大利亚昆士兰大学建立的高通量流程。在这个重点流程中,用于结构测定的目标是在小鼠巨噬细胞中表达且据推测在先天免疫中起作用的蛋白质。其目的是通过使用并行处理流程来表征这些目标的分子结构以及生化和细胞功能。该流程旨在处理数十至数百种目标基因产物,包括目标选择、克隆、表达、纯化、结晶和结构测定。此流程得出的结构将为先前未表征的巨噬细胞蛋白质的功能提供见解,并可能促成慢性阻塞性肺疾病和关节炎新药靶点的验证。

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