(taken from the application): Despite the importance of smooth muscle in health and disease, many details of its function and how it is regulated remain unclear. This renewal application is a continued effort to gain more insights into this area. The overall goal is to use molecular and cellular methodologies to obtain information on the functional roles of various smooth muscle proteins and to enhance our understanding of the regulatory mechanism of smooth muscle contraction. The program contains five projects, one facility core. Projects 0002 and 0004 deal with the thick filament regulation by investigating the mechanisms of myosin light chain kinase and myosin light chain phosphatase, respectively, by which the level of myosin activation is regulated. Project 0003 studies the structure and function of caldesmon to elucidate its roles in the thin filament-based regulation of smooth muscle contraction. Project 0008 is a new initiative to gain high-resolution structural information on the regulatory proteins in smooth muscles, starting with actin-caldesmon and myosin light chain phosphatase. In Project 0006 the integrated system of the thick and the thin filaments will be examined, and the role of tropomyosin in the cooperative properties of smooth muscle thin filament will be explored. This highly interactive and multi-disciplinary program utilizes a wide spectrum of different approaches, including analytical ultracentrifugation, chemical cross linking, fluorescence resonance energy transfer, circular dichroism, isothermal titration calorimetry, site-directed mutagenesis, X-ray crystallography, physiological measurements of smooth muscle tissues, and gene knockout experiments. In addition, rapid kinetics, chemical and enzymatic proteolysis, synthetic peptides, mass spectrometry and Immuno-electron microscopy will also be used. In particular, Project II proposes to use segmental isotope labeling techniques to study the structure of caldesmon by NMR spectroscopy. All subprojects will be supported by a ophysical/ Biochemical Core, which provides protein chemistry, analytical ultracentriftigation and electron microscopy and immunocytochemistry services. Funding of this program will enable us to expand our current investigation on the regulatory mechanisms in the smooth muscle system and lead to possible therapeutic measures of smooth muscle related diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Program Projects (P01)
Project #
5P01AR041637-14
Application #
7008157
Study Section
Special Emphasis Panel (ZAR1-RJB-B (J1))
Program Officer
Nuckolls, Glen H
Project Start
1992-09-30
Project End
2008-05-31
Budget Start
2005-12-01
Budget End
2007-05-31
Support Year
14
Fiscal Year
2006
Total Cost
$2,068,304
Indirect Cost
Name
Boston Biomedical Research Institute
Department
Type
DUNS #
058893371
City
Watertown
State
MA
Country
United States
Zip Code
02472
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