Molecular Mechanism of Pathogenesis

发病机制的分子机制

• 批准号: 7393692
• 负责人: JACK E DIXON
• 金额: $ 34.74万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN DIEGO
• 依托单位国家: 美国
• 财政年份: 2004
• 资助国家: 美国
• 起止时间: 2004-05-15 至 2010-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7393692
• 关键词: Actins; Address; Amino Acid Sequence; Arabidopsis RPS5 protein; Bacteria; Bacterial Infections; Biochemical; Biological Process; Bradyrhizobium; Cells; Cleaved cell; Complex; Cysteine Protease; Cytoskeleton; Disruption; Endopeptidases; Event; Family; Family member; Glycine decarboxylase; Lipids; Location; Membrane; Modification; Molecular; Pathogenesis; Peptide Hydrolases; Peptides; Phosphorylation; Plants; Play; Process; Protein Family; Proteins; Pseudomonas; Pseudomonas syringae; Resistance; Rhizobium; Roentgen Rays; Role; Signal Transduction; Site; Structure; System; Triad Acrylic Resin; Yersinia; genetic analysis; insight; member; mutant; research study; response; rho GTP-Binding Proteins

DESCRIPTION (provided by applicant): A Yersinia effector known as YopT and a Pseudomonas avirulence protein known as AvrPphB define a family of 19 proteins involved in bacterial pathogenesis. We show that both YopT and AvrPphB are cysteine proteases, and their proteolytic activities are dependent upon the invariant C/HID residues conserved in the entire YopT family. YopT cleaves the post-translationally modified Rho GTPases near their carboxyl termini, releasing them from the membrane. This leads to the disruption of actin cytoskeleton in host cells. The proteolytic activity of AvrPphB is essential for autoproteolytic cleavage of an AvrPphB precursor as well as for eliciting the hypersensitive response in plants. The biochemical functions of most avirulence (Avr) proteins are unknown. This proposal focuses on developing a molecular understanding of how the AvrPphB family of proteins is activated and post-translationally modified. In addition, efforts to identify the substrate(s) for AvrPphB are described. Finally, we propose to obtain the x-ray structure of AvrPphB complexed with a peptide substrate. These experiments will provide us with new insights into the molecular mechanism of pathogenesis.

描述（由申请人提供）：一种称为YOPT的Yersinia效应子和称为Avrpphb的假单胞菌促进蛋白，定义了与细菌发病机理有关的19个蛋白质家族。我们表明，Yopt和Avrpphb都是半胱氨酸蛋白酶，它们的蛋白水解活性取决于整个Yopt家族中保守的不变C/HID残基。 Yopt在其羧基末端附近裂解了翻译后修饰的Rho GTPase，从膜上释放出来。这导致宿主细胞中肌动蛋白细胞骨架的破坏。 AVRPPHB的蛋白水解活性对于AVRPPHB前体的自负解释以及引起植物中的超敏反应至关重要。大多数活力（AVR）蛋白的生化功能尚不清楚。该提案着重于对蛋白质蛋白的AVRPPHB家族如何被激活和翻译后修饰的分子理解。此外，描述了确定AVRPPHB底物的努力。最后，我们建议获得与肽底物复合的AVRPPHB的X射线结构。这些实验将为我们提供有关发病机理分子机制的新见解。

项目成果

A family of bacterial cysteine protease type III effectors utilizes acylation-dependent and -independent strategies to localize to plasma membranes.

• DOI: 10.1074/jbc.m900519200
• 发表时间: 2009-06-05
• 期刊: The Journal of biological chemistry
• 作者: Dowen RH;Engel JL;Shao F;Ecker JR;Dixon JE
• 通讯作者: Dixon JE

Subversion of myosin function by E. coli.

大肠杆菌破坏肌球蛋白功能。

• DOI: 10.1016/j.devcel.2007.12.016
• 发表时间: 2008
• 期刊: Developmental cell
• 影响因子: 11.8
• 作者: Mattoo,Seema;Alto,NealM;Dixon,JackE
• 通讯作者: Dixon,JackE

Structural basis of Fic-mediated adenylylation.

• DOI: 10.1038/nsmb.1867
• 发表时间: 2010-08
• 期刊: Nature structural & molecular biology
• 影响因子: 16.8

The fic domain: regulation of cell signaling by adenylylation.

• DOI: 10.1016/j.molcel.2009.03.008
• 发表时间: 2009-04-10
• 期刊: MOLECULAR CELL
• 影响因子: 16
• 作者: Worby, Carolyn A.;Mattoo, Seema;Kruger, Robert P.;Corbeil, Lynette B.;Koller, Antonius;Mendez, Juan C.;Zekarias, Bereket;Lazar, Cheri;Dixon, Jack E.
• 通讯作者: Dixon, Jack E.

Protection of mice against H. somni septicemia by vaccination with recombinant immunoglobulin binding protein subunits.

通过接种重组免疫球蛋白结合蛋白亚基来保护小鼠免受睡眠嗜血菌败血症。

• DOI: 10.1016/j.vaccine.2008.06.046
• 发表时间: 2008
• 期刊: Vaccine
• 影响因子: 5.5
• 作者: Geertsema,RogerS;Worby,Carolyn;Kruger,RobertP;Tagawa,Yuichi;Russo,Riccardo;Herdman,DScott;Lo,Kimby;Kimball,RichardA;Dixon,Jack;Corbeil,LynetteB
• 通讯作者: Corbeil,LynetteB