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Protein-protein interaction network and potential drug target candidates of Streptococcus suis

文献类型: 外文期刊

作者: Tan, M. -F. 1 ; Zou, G. 1 ; Wei, Y. 2 ; Liu, W. -Q. 1 ; Li, H. -Q. 2 ; Hu, Q. 1 ; Zhang, L. -S. 1 ; Zhou, R. 1 ;

作者机构: 1.Huazhong Agr Univ, State Key Lab Agr Microbiol, Coll Vet Med, Wuhan, Peoples R China

2.Jiangxi Acad Agr Sci, Inst Anim Husb & Vet Med, Nanchang, Jiangxi, Peoples R China

3.Minist Sci & Technol China, Int Res Ctr Anim Dis, Wuhan, Peoples R China

4.Cooperat Innovat Ctr Sustainable Pig Prod, Wuhan, Peoples R China

关键词: bacterial two‐ hybrid; drug target; FtsZ; homologous protein mapping; protein– protein interaction network; Streptococcus suis

期刊名称:JOURNAL OF APPLIED MICROBIOLOGY ( 影响因子:3.772; 五年影响因子:3.963 )

ISSN: 1364-5072

年卷期:

页码:

收录情况: SCI

摘要: Aims This study aimed to explore potential drug targets of Streptococcus suis at the system level. Methods and Results A homologous protein mapping method was used in the construction of a protein-protein interaction (PPI) network of S. suis, which presented 1147 non-redundant interaction pairs among 286 proteins. The parameters of PPI networks were calculated and showed scale-free network properties. In all, 41 possibly essential proteins identified from 47 highly connected proteins were selected as potential drug target candidates. Of these proteins, 30 were already regarded as drug targets in other bacterial species. Six transporters with high connections to other functional proteins were identified as probably not essential but important functional proteins. Afterward, the subnetwork centred with cell division protein FtsZ was used in confirming the PPI network through bacterial two-hybrid analysis. Conclusions The predicted PPI network covers 13 center dot 04% of the proteome in S. suis. The selected 41 potential drug target candidates are conserved between S. suis and several model bacteria. Significance and Impact of the Study The predictions included proteins known to be drug targets, and a verifying experiment confirmed the reliability of predicted interactions. This work is the first to present systematic computational PPI data for S. suis and provides potential drug targets, which are valuable in exploring novel anti-streptococcus drugs.

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