Preprotein Binding by the SecA ATPase
SecA ATP 酶结合前蛋白
基本信息
- 批准号:RGPIN-2018-05519
- 负责人:
- 金额:$ 2.62万
- 依托单位:
- 依托单位国家:加拿大
- 项目类别:Discovery Grants Program - Individual
- 财政年份:2022
- 资助国家:加拿大
- 起止时间:2022-01-01 至 2023-12-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
The research proposal addresses bacterial protein secretion, the process by which bacteria transport protein molecules from their site of synthesis inside the cell, to the exterior environment. All bacteria have a "General Secretory System" (GSS), or "Preprotein Translocase", that is able to recognize proteins that are destined for secretion (proteins with a secretory signal sequence, otherwise known as "preproteins"). Once they are recognized as secretory proteins, preproteins are prevented from folding, and then targeted to sites on the cell membrane where they can be passed through a pore to the outside environment, a process termed "translocation". The targeting and translocation processes are mediated by the SecA ATPase, which uses the energy of ATP hydrolysis to catalyze protein secretion.This GSS is absolutely required for bacterial growth, and is not present in mammalian cells. On this basis, the GSS, and in particular the SecA ATPase, are good potential targets for therapeutic antibiotics. In addition, certain bacteria, such as Mycobacterium tuberculosis, contain two SecA molecules, SecA1 and SecA2. SecA2 fulfills specialized functions including the secretion of virulence factors that allow the bacteria to survive in host cells. Therefore, increasing our understanding of how the GSS works could open new avenues for antimicrobial therapies. A deeper knowledge of GSS function will also enable the development of novel systems for protein expression and secretion in bacteria for biotechnological applications.The proposed research is focussed on understanding how SecA binds to its preprotein substrates. This binding interaction is important for the initial recognition of the preprotein, which takes place at the ribosome as the preprotein is synthesized, and ensures that the preprotein is correctly targeted to the secretion pathway. SecA-preprotein interactions are also important for translocation, where the preprotein is guided through a membrane pore by SecA.
该研究计划涉及细菌蛋白质分泌,即细菌将蛋白质分子从细胞内的合成位点运输到外部环境的过程。所有细菌都有一个“通用分泌系统”(GSS)或“前蛋白转位酶”,它能够识别注定要分泌的蛋白质(具有分泌信号序列的蛋白质,也称为“前蛋白”)。一旦它们被识别为分泌蛋白,前蛋白就被阻止折叠,然后靶向细胞膜上的位点,在那里它们可以通过孔到达外部环境,这一过程称为“易位”。靶向和转运过程由SecA ATP酶介导,该酶利用ATP水解的能量催化蛋白质分泌。这种GSS是细菌生长所必需的,而哺乳动物细胞中不存在。在此基础上,GSS,特别是SecA ATP酶,是治疗性抗生素的良好潜在靶点。此外,某些细菌,如结核分枝杆菌,含有两种SecA分子,SecA 1和SecA 2。SecA 2具有特殊的功能,包括分泌毒力因子,使细菌能够在宿主细胞中存活。因此,增加我们对GSS如何工作的理解可以为抗菌治疗开辟新的途径。对GSS功能的深入了解也将有助于开发用于生物技术应用的细菌蛋白表达和分泌的新系统。拟议的研究重点是了解SecA如何与其前蛋白底物结合。这种结合相互作用对于前蛋白的初始识别是重要的,其在前蛋白合成时发生在核糖体处,并确保前蛋白正确地靶向分泌途径。SecA-前蛋白相互作用对于易位也很重要,其中前蛋白被SecA引导通过膜孔。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Shilton, Brian其他文献
Specific quinone reductase 2 inhibitors reduce metabolic burden and reverse Alzheimer's disease phenotype in mice.
- DOI:
10.1172/jci162120 - 发表时间:
2023-10-02 - 期刊:
- 影响因子:15.9
- 作者:
Gould, Nathaniel L.;Scherer, Gila R.;Carvalho, Silvia;Shurrush, Khriesto;Kayyal, Haneen;Edry, Efrat;Elkobi, Alina;David, Orit;Foqara, Maria;Thakar, Darshit;Pavesi, Tommaso;Sharma, Vijendra;Walker, Matthew;Maitland, Matthew;Dym, Orly;Albeck, Shira;Peleg, Yoav;Germain, Nicolas;Babaev, Ilana;Sharir, Haleli;Lalzar, Maya;Shklyar, Boris;Hazut, Neta;Khamaisy, Mohammad;Levesque, Maxime;Lajoie, Gilles;Avoli, Massimo;Amitai, Gabriel;Lefker, Bruce;Subramanyam, Chakrapani;Shilton, Brian;Barr, Haim;Rosenblum, Kobi - 通讯作者:
Rosenblum, Kobi
Shilton, Brian的其他文献
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{{ truncateString('Shilton, Brian', 18)}}的其他基金
Preparative Ultracentrifuge and Rotors for Western BioCORE Facility
用于 Western BioCORE 设施的制备型超速离心机和转头
- 批准号:
RTI-2023-00211 - 财政年份:2022
- 资助金额:
$ 2.62万 - 项目类别:
Research Tools and Instruments
Preprotein Binding by the SecA ATPase
SecA ATP 酶结合前蛋白
- 批准号:
RGPIN-2018-05519 - 财政年份:2021
- 资助金额:
$ 2.62万 - 项目类别:
Discovery Grants Program - Individual
Preprotein Binding by the SecA ATPase
SecA ATP 酶结合前蛋白
- 批准号:
RGPIN-2018-05519 - 财政年份:2020
- 资助金额:
$ 2.62万 - 项目类别:
Discovery Grants Program - Individual
Preprotein Binding by the SecA ATPase
SecA ATP 酶结合前蛋白
- 批准号:
RGPIN-2018-05519 - 财政年份:2019
- 资助金额:
$ 2.62万 - 项目类别:
Discovery Grants Program - Individual
Preprotein Binding by the SecA ATPase
SecA ATP 酶结合前蛋白
- 批准号:
RGPIN-2018-05519 - 财政年份:2018
- 资助金额:
$ 2.62万 - 项目类别:
Discovery Grants Program - Individual
Conformational Switching and Energetics in the Maltose Transporter
麦芽糖转运蛋白的构象转换和能量学
- 批准号:
217494-2013 - 财政年份:2017
- 资助金额:
$ 2.62万 - 项目类别:
Discovery Grants Program - Individual
Conformational Switching and Energetics in the Maltose Transporter
麦芽糖转运蛋白的构象转换和能量学
- 批准号:
217494-2013 - 财政年份:2016
- 资助金额:
$ 2.62万 - 项目类别:
Discovery Grants Program - Individual
Conformational Switching and Energetics in the Maltose Transporter
麦芽糖转运蛋白的构象转换和能量学
- 批准号:
217494-2013 - 财政年份:2015
- 资助金额:
$ 2.62万 - 项目类别:
Discovery Grants Program - Individual
Conformational Switching and Energetics in the Maltose Transporter
麦芽糖转运蛋白的构象转换和能量学
- 批准号:
217494-2013 - 财政年份:2014
- 资助金额:
$ 2.62万 - 项目类别:
Discovery Grants Program - Individual
Conformational Switching and Energetics in the Maltose Transporter
麦芽糖转运蛋白的构象转换和能量学
- 批准号:
217494-2013 - 财政年份:2013
- 资助金额:
$ 2.62万 - 项目类别:
Discovery Grants Program - Individual
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