HIGH RESOLUTION EM OF NUDAURELIA CAPENSIS OMEGA VIRUS (NWV) MUTANTS
HIGH RESOLUTION EM OF NUDAURELIA CAPENSIS OMEGA VIRUS (NWV) MUTANTS
批准号:
7602764
负责人:
JOAN JOHNSON
金额:
$0.89万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-08-13 至 2008-07-31
关键词:
Active SitesCaliberCleaved cellComplexComputer Retrieval of Information on Scientific Projects DatabaseEnvironmentFundingGrantHalf-LifeIn VitroInstitutionLeftModelingMutationParticle SizePhenotypeProcessProteolysisReporterResearchResearch PersonnelResolutionResourcesRestRoentgen RaysSiteSourceStructureTimeUnited States National Institutes of HealthVirusbasemutantparticlepolypeptide
中文摘要
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英文摘要
This subproject is one of many research subprojects utilizing the
resources provided by a Center grant funded by NIH/NCRR. The subproject and
investigator (PI) may have received primary funding from another NIH source,
and thus could be represented in other CRISP entries. The institution listed is
for the Center, which is not necessarily the institution for the investigator.
Virus maturation occurs in virtually all complex viruses. Following maturation the virus acquires infectivity and usually the stability required for the extra-cellular environment. We used Nudaurelia Capensis omega virus (NwV) as a model to understand this process and to control it by mutation.
The NwV procapsid is 480 A diameter and formed by240, 70kDa subunits. The mature particle is 410 A in diameters and is formed by 240 copies of residues 1-570 (beta) and 240 copies of the polypeptide 571-644 (gamma). The autocatalysis of alpha (1-644) to beta + gamma is a convenient reporter of maturation. In vitro, maturation is initiated by lowering the pH from 7.5 to 4.0. The particle size changes in less than one second and the cleavage has a half life of approximately 45 min at pH=5.0. Based on the previously determined X-ray structure mutations were made and characterized by examining the extent of subunit proteolysis. One mutant displaying an intriguing phenotype was E73Q. Within experimental error 50% of the subunits cleaved, leaving the rest uncleaved for an extended period of time. This suggested that we selectively perturbed the autocatalytic site in half the subunits and that this was probably due to a perturbation of subunit contacts that are required for completing the active site.
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MG2+ BLOCK AND CA2+ SELECTIVITY IN THE NMDA RECEPTOR
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批准号:8364297
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项目类别:
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资助金额:$0.11万
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财政年份:2011
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负责人:JOAN JOHNSON
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依托单位:
STRUCTURAL MODELING OF THE NMDA RECEPTOR CHANNEL
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批准号:8171850
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项目类别:
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资助金额:$0.11万
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财政年份:2010
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负责人:JOAN JOHNSON
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依托单位:
MG2+ BLOCK AND CA2+ SELECTIVITY IN THE NMDA RECEPTOR
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批准号:8171913
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项目类别:
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资助金额:$0.11万
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财政年份:2010
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负责人:JOAN JOHNSON
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依托单位:
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批准号:7956155
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项目类别:
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资助金额:$0.08万
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财政年份:2009
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负责人:JOAN JOHNSON
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依托单位:
STRUCTURAL MODELING OF THE NMDA RECEPTOR CHANNEL
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批准号:7723285
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项目类别:
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资助金额:$0.05万
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财政年份:2008
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负责人:JOAN JOHNSON
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依托单位:
HIGH RESOLUTION STRUCTURE OF BACTERIOPHAGE P22
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批准号:7602734
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项目类别:
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资助金额:$3.58万
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财政年份:2007
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负责人:JOAN JOHNSON
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依托单位:
STRUCTURAL MODELING OF THE NMDA RECEPTOR CHANNEL
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批准号:7601548
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项目类别:
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资助金额:$0.03万
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财政年份:2007
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负责人:JOAN JOHNSON
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依托单位:
HIGH RESOLUTION STRUCTURE OF BACTERIOPHAGE P2
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批准号:7369612
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项目类别:
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资助金额:$2.52万
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财政年份:2006
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负责人:JOAN JOHNSON
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依托单位:
CONFORMATIONAL CHANGE IN ICOSAHEDRAL VIRUSES
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批准号:7181256
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项目类别:
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资助金额:$0.96万
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财政年份:2005
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负责人:JOAN JOHNSON
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依托单位:
HIGH RESOLUTION STRUCTURE OF BACTERIOPHAGE P22
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批准号:7183088
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项目类别:
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资助金额:$1.31万
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财政年份:2005
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负责人:JOAN JOHNSON
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依托单位:
海外基金