This subproject is one of many research subprojects utilizing theresources provided by a Center grant funded by NIH/NCRR. The subproject andinvestigator (PI) may have received primary funding from another NIH source,and thus could be represented in other CRISP entries. The institution listed isfor the Center, which is not necessarily the institution for the investigator.The principle mechanism responsible for the contraction and relaxation of smooth muscle involves the reversible phosphorylation of the 20 kDa regulatory myosin light chain (rMLC). Typically, elevations in intracellular Ca2+ result in rMLC phosphorylation at the serine-19 (or adjacent threonine-18) residue by the Ca2+/calmodulin-activated MLC kinase (MLCK). The studies in this collaboration are intended to extend findings with respect to the physiological importance of this alternate-site phosphorylation in vascular smooth muscle, and the signaling pathways involved. Continued studies are proposed using accurate mass-driven analysis and rapid parallel MS/MS acquisition to further identify and clarify the physiological conditions under which this alternate site rMLC phosphorylation occurs.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR000954-31
Application #
7721488
Study Section
Special Emphasis Panel (ZRG1-BPC-H (40))
Project Start
2008-02-01
Project End
2009-01-31
Budget Start
2008-02-01
Budget End
2009-01-31
Support Year
31
Fiscal Year
2008
Total Cost
$1,604
Indirect Cost
Name
Washington University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
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