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. Assembly and disassembly of a viral capsid, or a protein shell, are essential steps in the life cycle of a virus. Understanding of viral assembly/disassembly can provide additional insights to other oligomerization processes as in protein association in large cellular assemblies, which occurs through a similar mechanism. Additionally, understanding the properties and function of the capsid shell alone is important for inferring all steps involved in host cell entry and release of the enveloped genetic material and can aid in proposing efficient ways of interfering with capsid assembly and stability via structure-based design of antiviral therapeutics. One of the most intensely studied viruses has been the cowpea chlorotic mottle virus (CCMV), a positive strand RNA plant-infecting virus which belongs to the Bromoviridae family. It is composed of a protein capsid and viral RNA which is packed inside. It has been widely used as a model system for understanding of biological assembly because of its icosahedral structure and the limited number of gene products required for its assembly. CCMV offers an accessible model system for examining the processes that regulate viral assembly, disassembly, and stability, both for theoretical and experimental studies.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
2P41RR008605-16
Application #
7955247
Study Section
Special Emphasis Panel (ZRG1-SBIB-C (40))
Project Start
2009-05-01
Project End
2010-04-30
Budget Start
2009-05-01
Budget End
2010-04-30
Support Year
16
Fiscal Year
2009
Total Cost
$3,181
Indirect Cost
Name
University of California San Diego
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
804355790
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Pantoja, Joe Luis; Morgan, Ashley E; Grossi, Eugene A et al. (2017) Undersized Mitral Annuloplasty Increases Strain in the Proximal Lateral Left Ventricular Wall. Ann Thorac Surg 103:820-827
Morgan, Ashley E; Wozniak, Curtis J; Gulati, Sarthak et al. (2017) Association of Uneven MitraClip Application and Leaflet Stress in a Finite Element Model. JAMA Surg 152:111-114
Morgan, Ashley E; Pantoja, Joe L; Grossi, Eugene A et al. (2016) Neochord placement versus triangular resection in mitral valve repair: A finite element model. J Surg Res 206:98-105
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Ebeida, Mohamed S; Rushdi, Ahmad A; Awad, Muhammad A et al. (2016) Disk Density Tuning of a Maximal Random Packing. Comput Graph Forum 35:259-269
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Watson, Shana R; Liu, Piaomu; Peña, Edsel A et al. (2016) Comparison of Aortic Collagen Fiber Angle Distribution in Mouse Models of Atherosclerosis Using Second-Harmonic Generation (SHG) Microscopy. Microsc Microanal 22:55-62
Ge, Liang; Wu, Yife; Soleimani, Mehrdad et al. (2016) Moderate Ischemic Mitral Regurgitation After Posterolateral Myocardial Infarction in Sheep Alters Left Ventricular Shear but Not Normal Strain in the Infarct and Infarct Borderzone. Ann Thorac Surg 101:1691-9
Morgan, Ashley E; Pantoja, Joe Luis; Weinsaft, Jonathan et al. (2016) Finite Element Modeling of Mitral Valve Repair. J Biomech Eng 138:021009

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