Mining Multiple Solvent Crystal Structures for Properties of Protein Binding Sites
挖掘多种溶剂晶体结构以了解蛋白质结合位点的特性
基本信息
- 批准号:0818678
- 负责人:
- 金额:$ 57.65万
- 依托单位:
- 依托单位国家:美国
- 项目类别:Continuing Grant
- 财政年份:2008
- 资助国家:美国
- 起止时间:2008-08-01 至 2012-04-30
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Intellectual meritProteins are biological polymers that fold into specific three-dimensional structures. They are the molecular workhorses of life and are involved in a wide variety of functions such as increasing the rates of chemical reactions, storing and transporting small molecules such as oxygen, mediating the propagation of signals or "instructions" within the cell and much more. Most protein function involves binding to a small molecule or another protein through special features on the surface within so-called binding sites. Dr. Mattos and members of her group are interested in understanding the features that distinguish binding sites on proteins from other areas on the protein surface. This project aims to do this by observing how a variety of small molecules bind to a set of well-studied proteins using a method called X-ray crystallography that allows visualization of the three-dimensional structure of proteins and the associated small molecules at near atomic resolution. The Mattos lab has collected the experimental data sets necessary for this type of analysis and is now using computational methods to mine the data sets for fundamental properties of protein surfaces in general and binding sites in particular. The quantitative methods will be used to validate the correspondence between protein surface properties obtained in the small molecule solvent environment and those observed in the more natural aqueous environment. Once the validation is complete the fundamental protein binding site properties will be directly obtained from experimental data sets acquired in the non-natural solvent environment. Understanding the properties of protein binding sites is critical to understanding of how proteins work and therefore a very important step in making sense of the complicated processes of life.Broader impactDr. Mattos has developed this project in such a way that research is an integral part of teaching undergraduates. The research will build on the thriving and diverse educational environment that she has already created in her group. Ten undergraduates from her classes each year will be invited to work with graduate students and the more senior members of the laboratory. The team will participate in an international collaboration with Prof. Janet Thornton's group at the European Bioinformatics Institute (EBI) in England, which is at the forefront of computational analysis of protein experimental databases. Dr. Mattos has recently returned from a sabbatical at the EBI, during which both a graduate and an undergraduate student also participated. She plans to continue to engage students in this international collaboration. In addition, Dr. Mattos is involved in mentoring minority junior faculty members at various universities in the United States and is working to encourage minority undergraduate and graduate students at North Carolina State University to write research proposals for fellowship applications to graduate school.
智能优点蛋白质是一种生物聚合物,可以折叠成特定的三维结构。它们是生命中的分子主力,参与各种功能,如加快化学反应速度,储存和运输氧气等小分子,调节细胞内信号或“指令”的传播等。大多数蛋白质的功能涉及通过所谓的结合位点内表面的特殊功能与一个小分子或另一种蛋白质结合。马托斯博士和她的团队成员对了解蛋白质结合部位与蛋白质表面其他区域的区别特征很感兴趣。该项目旨在通过使用一种名为X射线结晶学的方法观察各种小分子如何与一系列研究良好的蛋白质结合来实现这一点,这种方法可以在接近原子分辨率的情况下可视化蛋白质及其相关小分子的三维结构。马托斯实验室已经收集了这类分析所需的实验数据集,现在正在使用计算方法来挖掘蛋白质表面一般和特别是结合位点的基本性质的数据集。定量方法将被用来验证在小分子溶剂环境中获得的蛋白质表面性质与在更自然的水环境中观察到的蛋白质表面性质之间的一致性。一旦验证完成,将直接从在非天然溶剂环境中获得的实验数据集获得基本的蛋白质结合位点属性。了解蛋白质结合部位的性质对于了解蛋白质是如何工作的至关重要,因此也是理解生命复杂过程的重要一步。马托斯开发这个项目的方式是,研究是本科生教学中不可或缺的一部分。这项研究将建立在她已经在她的团队中创造的蓬勃发展和多样化的教育环境之上。每年,她班上的10名本科生将被邀请与研究生和实验室更资深的成员一起工作。该团队将参与英国欧洲生物信息学研究所(EBI)珍妮特·桑顿教授的国际合作,该研究所处于蛋白质实验数据库计算分析的前沿。马托斯博士最近刚从EBI休假归来,在此期间,一名研究生和一名本科生也参加了这次活动。她计划继续让学生参与到这个国际合作中来。此外,马托斯博士还参与指导美国多所大学的少数族裔初级教职员工,并鼓励北卡罗来纳州立大学的少数族裔本科生和研究生为研究生院的奖学金申请撰写研究计划书。
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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Carla Mattos其他文献
Locating and characterizing binding sites on proteins
定位和表征蛋白质上的结合位点
- DOI:
10.1038/nbt0596-595 - 发表时间:
1996-05-01 - 期刊:
- 影响因子:41.700
- 作者:
Carla Mattos;Dagmar Ringe - 通讯作者:
Dagmar Ringe
Analysis of two-residue turns in proteins.
蛋白质中两个残基转角的分析。
- DOI:
- 发表时间:
1994 - 期刊:
- 影响因子:5.6
- 作者:
Carla Mattos;G. Petsko;M. Karplus - 通讯作者:
M. Karplus
Mass spectrometry methods and mathematical PK/PD model for decision tree-guided covalent drug development
用于决策树指导的共价药物开发的质谱方法和数学药代动力学/药效学模型
- DOI:
10.1038/s41467-025-56985-6 - 发表时间:
2025-02-19 - 期刊:
- 影响因子:15.700
- 作者:
Md Amin Hossain;Rutali R. Brahme;Brandon C. Miller;Jakal Amin;Marcela de Barros;Jaime L. Schneider;Jared R. Auclair;Carla Mattos;Qingping Wang;Nathalie Y. R. Agar;David J. Greenblatt;Roman Manetsch;Jeffrey N. Agar - 通讯作者:
Jeffrey N. Agar
Carla Mattos的其他文献
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{{ truncateString('Carla Mattos', 18)}}的其他基金
Allosteric effects in the complexes between Ras proteins and Raf
Ras 蛋白和 Raf 复合物的变构效应
- 批准号:
2121426 - 财政年份:2021
- 资助金额:
$ 57.65万 - 项目类别:
Standard Grant
Allosteric elements in the superfamily of small GTPases
小 GTP 酶超家族中的变构元素
- 批准号:
1517295 - 财政年份:2015
- 资助金额:
$ 57.65万 - 项目类别:
Standard Grant
REU Site: Research Opportunities in Biological and Chemical Catalysis
REU 网站:生物和化学催化领域的研究机会
- 批准号:
1262734 - 财政年份:2013
- 资助金额:
$ 57.65万 - 项目类别:
Standard Grant
Mechanism of Intrinsic Hydrolysis in Small GTPases
小 GTP 酶的固有水解机制
- 批准号:
1244203 - 财政年份:2013
- 资助金额:
$ 57.65万 - 项目类别:
Continuing Grant
Mining Multiple Solvent Crystal Structures for Properties of Protein Binding Sites
挖掘多种溶剂晶体结构以了解蛋白质结合位点的特性
- 批准号:
1237512 - 财政年份:2012
- 资助金额:
$ 57.65万 - 项目类别:
Continuing Grant
MRI: Acquisition of X-Ray protein crystallography equipment at Northeastern University
MRI:购置东北大学X射线蛋白质晶体学设备
- 批准号:
1228897 - 财政年份:2012
- 资助金额:
$ 57.65万 - 项目类别:
Standard Grant
PECASE: Probing protein surfaces using multiple solvent crystal structures
PECASE:使用多种溶剂晶体结构探测蛋白质表面
- 批准号:
0237297 - 财政年份:2003
- 资助金额:
$ 57.65万 - 项目类别:
Continuing Grant
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