Defining the role of site-specific proteolysis in innate defense signaling
Defining the role of site-specific proteolysis in innate defense signaling
批准号:
10650829
负责人:
Mohsan Saeed
金额:
$41.25万
依托单位国家:
美国
项目类别:
财政年份:
2022
资助国家:
美国
项目状态:
未结题
起止时间:
2022-07-01 至 2027-04-30
关键词:
AcetylationAwardCellsDefense MechanismsDevelopmentDiseaseEnvironmentFunctional disorderGoalsHumanInnate Immune ResponseInvadedInvestigationKnowledgeLabelMissionMolecular BiologyN-terminalOrganPathway interactionsPeptide HydrolasesPerformancePhosphorylationPost-Translational Modification SitePost-Translational Protein ProcessingProcessProteinsProteolysisProteolytic ProcessingRegulationResearchResolutionRoleSignal TransductionSiteSystems BiologyTissuesToxinUbiquitinationUnited States National Institutes of HealthViralcell growth regulationdefense responsedesignexperienceimprovedinsightmicrobialmicrobial diseasepathogenpotential biomarkertherapeutic target
中文摘要
点击翻译按钮获取中文摘要
英文摘要
PROJECT SUMMARY
Human cells respond to foreign agents such as pathogens and toxins by initiating a strong innate defense
response that creates a protective environment in the cells and incapacitates the invading pathogens and
foreign substances. The initiation, activation, and resolution of this innate defense response is a carefully
regulated process designed to avoid both hyperactivation and underactivation, either of which can lead to
tissue damage, organ dysfunction, and microbial diseases.
A key strategy that cells use to achieve tight regulatory control of innate defense signaling is the alteration of
protein post-translational modifications (PTMs: phosphorylation, ubiquitination, acetylation, etc.). The goal of
my lab for the next five years will be to explore the role of an understudied PTM, the site-specific proteolysis,
in regulating innate defense signaling. I have extensive experience in studying antiviral innate immune
responses, and have recently optimized a robust protein N-terminal labeling approach that provides an
unbiased view of site-specific proteolysis in cells — expertise that will enable me to decipher the regulatory
functions of site-specific proteolysis in innate defense mechanisms.
With this MIRA award, my group will pursue two specific research directions. First, we will determine the role
of the proteolytic N-end rule pathway in controlling the stability of proteins involved in defense signaling.
Second, we will investigate the ways in which internal protein cleavages activate defense responses. For the
proposed studies, we will employ a combination of focused molecular biology investigations and systems
biology approaches, such as activity-based protease profiling and protein N-terminal labeling. These efforts
will generate new knowledge about the role of proteases in the regulation of cellular defenses and inform the
development of strategies to improve the performance of innate defense mechanisms against escalating
microbial and environmental threats.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Functional characterization of the enteroviral degradome
-
批准号:10503958
-
项目类别:
-
资助金额:$51.98万
-
财政年份:2022
-
负责人:Mohsan Saeed
-
依托单位:
Defining the role of site-specific proteolysis in innate defense signaling
-
批准号:10500999
-
项目类别:
-
资助金额:$41.25万
-
财政年份:2022
-
负责人:Mohsan Saeed
-
依托单位:
Functional characterization of the enteroviral degradome
-
批准号:10661758
-
项目类别:
-
资助金额:$51.08万
-
财政年份:2022
-
负责人:Mohsan Saeed
-
依托单位:
海外基金