EVOLUTION OF THE RIBONUCLEASE SUPERFAMILY
核糖核酸酶超家族的进化
基本信息
- 批准号:6386317
- 负责人:
- 金额:$ 14.57万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1998
- 资助国家:美国
- 起止时间:1998-09-01 至 2003-08-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
DESCRIPTION: The goal of this grant is to develop a new strategy for
joining physiological function to biochemical behavior in proteins. This
approach combines protein structure, mechanism, and engineering with
evolutionary analyses. Central to this analysis is the reconstruction of
evolutionary history of the protein superfamily from sequence data, and
preparing ancient proteins from extinct organisms in the laboratory where
they can be studied. The evolution of molecular and biological behavior is
set in a historical context by correlating it with the evolution of
organisms (deduced from paleontology) and the surrounding ecology, allowing
construction of testable hypotheses concerning the structure-behavior
relationships in this family, mechanisms by which these compounds exert
their biological activities, and possible physiological function(s) of the
proteins, as well as allowing to engineer new proteins with desired
behaviors. The work here will use ribonuclease as a system to develop this
strategy. Bovine pancreatic RNase A belongs to a superfamily of proteins
that has, in various members, evolved to an enormous range of interesting
biological behaviors. RNase homologs are known that are immunosuppressive,
block the growth of tumor cells (But not normal cells), kill Schistosoma and
Trichinella, cause neurological damage, cause lung damage in asthmatic
patients, display lectin-like behavior, inhibit infection of mammalian cells
by HIV-1, or do none of these. These behaviors have medical relevance;
several RNase variants are now in clinical and preclinical stages of testing
for their useful biomedical activities. In the next phase of this ongoing
research program, the physiological significance of biological behaviors of
seminal RNase will be assessed, a crystal structure solved to determine the
mechanism by which seminal RNase binds and melts duplex DNA, the impact of
the introduction of cysteines on the kinetics of folding and the
thermodynamics of the folded structure will be examined and new sequence
data will be collected to complete the model of the evolutionary history of
this important class of molecules. This study will show how new
biomolecular function is created in higher organisms, by mutation,
insertion, deletion gene duplication and recruitment of duplicate genes.
This evolutionary approach differs from that pursued in other laboratories,
and this work will continue to develop a new paradigm where evolutionary
information is integrated with chemical and biological information to solve
biomedical research problems in a "post-genome" environment.
描述:这笔赠款的目标是制定一项新的战略
在蛋白质中将生理功能与生化行为结合起来。这
方法将蛋白质的结构、机制和工程学与
进化论分析。这一分析的核心是重建
来自序列数据的蛋白质超家族的进化历史,以及
在实验室里从灭绝的生物体中制备古代蛋白质
它们是可以研究的。分子和生物行为的进化是
设置在历史背景下,将其与
生物体(源自古生物学)和周围的生态,允许
关于结构-行为的可验证性假设的构造
在这个家族中的关系,这些化合物发挥作用的机制
它们的生物学活动,以及可能的生理功能(S)
蛋白质,以及允许对所需的新蛋白质进行工程
行为。这里的工作将使用核糖核酸酶作为一种系统来开发这种
策略。牛胰腺核糖核酸酶A属于蛋白质超家族
在不同的成员中,这已经演变成了一系列有趣的
生物学行为。已知的核糖核酸酶同系物具有免疫抑制作用,
阻断肿瘤细胞(但不是正常细胞)的生长,杀死血吸虫和
旋毛虫引起神经损伤,导致哮喘患者肺损伤
患者表现出凝集素样行为,抑制哺乳动物细胞的感染
被HIV-1感染,或者什么都不做。这些行为与医学有关;
几种核糖核酸酶变体目前正处于临床和临床前测试阶段
因为他们有用的生物医学活动。在正在进行的下一阶段
研究计划,生物行为的生理学意义
将对种子核糖核酸酶进行评估,解决晶体结构问题以确定
精液核糖核酸酶结合和融化双链DNA的机制,
介绍了半胱氨酸对折叠动力学的影响以及半胱氨酸对折叠的影响。
将对褶皱结构的热力学进行研究,并对新的序列
将收集数据以完成生物进化历史的模型
这类重要的分子。这项研究将展示新的
生物分子功能是在高等生物体中通过突变而产生的,
插入、缺失、基因复制和重复基因的招募。
这种进化方法不同于其他实验室所采用的方法,
这项工作将继续发展一种新的范式,即进化
将信息与化学和生物信息整合起来解决
“后基因组”环境下的生物医学研究问题。
项目成果
期刊论文数量(3)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Evolutionary history of the uterine serpins.
子宫丝氨酸蛋白酶抑制剂的进化史。
- DOI:
- 发表时间:2000
- 期刊:
- 影响因子:0
- 作者:Peltier,MR;Raley,LC;Liberles,DA;Benner,SA;Hansen,PJ
- 通讯作者:Hansen,PJ
Analysis of transitions at two-fold redundant sites in mammalian genomes. Transition redundant approach-to-equilibrium (TREx) distance metrics.
哺乳动物基因组中两倍冗余位点的转变分析。
- DOI:10.1186/1471-2148-6-25
- 发表时间:2006
- 期刊:
- 影响因子:3.4
- 作者:Li,Tang;Chamberlin,StephenG;Caraco,MDaniel;Liberles,DavidA;Gaucher,EricA;Benner,StevenA
- 通讯作者:Benner,StevenA
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STEVEN A BENNER其他文献
STEVEN A BENNER的其他文献
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{{ truncateString('STEVEN A BENNER', 18)}}的其他基金
Basic Research for Diagnostics and Surveillance in Lower Resource Environments
低资源环境诊断和监测基础研究
- 批准号:
10669039 - 财政年份:2021
- 资助金额:
$ 14.57万 - 项目类别:
Easily Used Kits to Evolve Reagents that Covalently Tag and Inactivate Proteins
易于使用的试剂盒可进化出共价标记和灭活蛋白质的试剂
- 批准号:
10626917 - 财政年份:2021
- 资助金额:
$ 14.57万 - 项目类别:
Basic Research for Diagnostics and Surveillance in Lower Resource Environments
低资源环境诊断和监测基础研究
- 批准号:
10468606 - 财政年份:2021
- 资助金额:
$ 14.57万 - 项目类别:
Easily Used Kits to Evolve Reagents that Covalently Tag and Inactivate Proteins
易于使用的试剂盒可进化出共价标记和灭活蛋白质的试剂
- 批准号:
10478279 - 财政年份:2021
- 资助金额:
$ 14.57万 - 项目类别:
Easily Used Kits to Evolve Reagents that Covalently Tag and Inactivate Proteins
易于使用的试剂盒可进化出共价标记和灭活蛋白质的试剂
- 批准号:
10298982 - 财政年份:2021
- 资助金额:
$ 14.57万 - 项目类别:
Equipment Supplement to 1R01GM141391-01A1 (Easily Used Kits to Evolve Reagents that Covalently Tag and Inactivate Proteins)
1R01GM141391-01A1 的设备补充(易于使用的试剂盒,用于进化共价标记和灭活蛋白质的试剂)
- 批准号:
10580301 - 财政年份:2021
- 资助金额:
$ 14.57万 - 项目类别:
PHS2019-02 Omnibus Solic of the NIH, CDC, and FDA for SBIR Apps No Clinical Trial (Parent SBIR R43/4
PHS2019-02 NIH、CDC 和 FDA 的 SBIR 应用程序综合 Solic 尚未进行临床试验(母公司 SBIR R43/4
- 批准号:
10476977 - 财政年份:2021
- 资助金额:
$ 14.57万 - 项目类别:
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