人类龋齿致病菌变形链球菌的结构基因组学研究。

Lanfen Li, Jie Nan, Dan Li, Erik Brostromer, Zixi Wang, Cong Liu, Qiaoming Hou, Xuexin Fan, Zhaoyang Ye, Xiao-Dong Su
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引用次数: 7

摘要

革兰氏阳性细菌变形链球菌是人类龋齿的主要病原体。为了在原子结构水平上更好地了解这种病原体,并建立潜在的药物和疫苗靶点,我们自2005年以来开展了结构基因组学研究。为了实现这一目标,我们开发了多种内部自动化系统,包括新型高通量结晶设备和方法,并在此基础上建立了大型,高效,低成本的实验室平台。从1963个带注释的开放阅读框中,选择1391个非膜靶点,根据蛋白质序列与未知结构的相似性进行优先排序,并根据限制性位点进行聚类,以实现经济高效的高通量常规克隆。选择的蛋白在不同的大肠杆菌菌株中过表达。选择表达可溶性蛋白的克隆,扩增,纯化表达蛋白并进行结晶试验。最后,对蛋白质晶体进行x射线分析,并用晶体学方法确定其结构。利用先前建立的程序,我们迄今已经获得了200多种蛋白质晶体和100种涉及不同生物途径的晶体结构。在本文中,我们展示并回顾了在中等实验室规模进行结构基因组学研究的可能性。此外,我们的研究开发的技术和方法可以广泛应用于传统的结构生物学研究实践。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Structural genomics studies of human caries pathogen Streptococcus mutans.

Gram-positive bacterium Streptococcus mutans is the primary causative agent of human dental caries. To better understand this pathogen at the atomic structure level and to establish potential drug and vaccine targets, we have carried out structural genomics research since 2005. To achieve the goal, we have developed various in-house automation systems including novel high-throughput crystallization equipment and methods, based on which a large-scale, high-efficiency and low-cost platform has been establish in our laboratory. From a total of 1,963 annotated open reading frames, 1,391 non-membrane targets were selected prioritized by protein sequence similarities to unknown structures, and clustered by restriction sites to allow for cost-effective high-throughput conventional cloning. Selected proteins were over-expressed in different strains of Escherichia coli. Clones expressed soluble proteins were selected, expanded, and expressed proteins were purified and subjected to crystallization trials. Finally, protein crystals were subjected to X-ray analysis and structures were determined by crystallographic methods. Using the previously established procedures, we have so far obtained more than 200 kinds of protein crystals and 100 kinds of crystal structures involved in different biological pathways. In this paper we demonstrate and review a possibility of performing structural genomics studies at moderate laboratory scale. Furthermore, the techniques and methods developed in our study can be widely applied to conventional structural biology research practice.

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