The overall goal of the applicant's research is to have a detailed understanding of how muscle contraction is regulated at the cellular and molecular levels by myofibrillar protein isoforms, and to transfer this information from basic science into practical clinical knowledge in muscle disorders affecting myosin and myosin-associated proteins in humans. A large proportion of patients evaluated for skeletal muscle weakness still fail to receive specific diagnosis, but improvement of molecular diagnostic tools together with structure-function analyzes of the motor protein myosin will provide the basis for screening patients for possible skeletal myosinopathies. The maximum velocity of unloading shortening (Vo) is one of the most important design parameters of skeletal muscle since muscles develop their maximum power at a shortening velocity of approximately one-third Vo and detailed understanding of Vo regulation and modulation by myofibrillar proteins is of significant importance in both basic and clinical science. This project, focusing on changes in shortening velocity associated with a change in body size (scaling), constitutes a significant component in our attempt to further elucidate the regulation and modulation of muscle contraction in mammalian skeletal muscle. Our knowledge on the regulation of muscle contraction and expression of myofibrillar protein isoforms is primarily based observations in rodents, but there is reason to question whether results from small mammals, such as the rat, can be generalized to larger mammals, such as man, constituting a 250-fold difference in body size. There is accordingly a significant need for projects focusing on the mechanisms underlying scaling-related differences in shortening velocity at the cellular and molecular levels. A combination of biochemical, mass spectrometry, cellular- and molecular-physiological techniques will be used to explore the regulatory and modulatory influence of different contractile protein isoforms on shortening velocity in mammals with a 25,000-fold body size range.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Project (R01)
Project #
1R01AR047318-01A1
Application #
6399308
Study Section
Geriatrics and Rehabilitation Medicine (GRM)
Program Officer
Lymn, Richard W
Project Start
2001-07-13
Project End
2006-06-30
Budget Start
2001-07-13
Budget End
2002-06-30
Support Year
1
Fiscal Year
2001
Total Cost
$281,061
Indirect Cost
Name
Pennsylvania State University
Department
Miscellaneous
Type
Schools of Allied Health Profes
DUNS #
City
University Park
State
PA
Country
United States
Zip Code
16802
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