The objective of this program is to determine the precise molecular architecture of a diverse class of Alpha-fibrous proteins whose role is both structural and dynamic. The chief methods are coordinated X-ray crystallography, electron microscopy and image analysis. Muscle proteins are a central focus and provide the background for studying related systems. A major aim is to determine the structure and motions in two calcium-dependent protein switches that control contraction. Thus crystals of the regulatory complex tropomyosin/troponin are being analyzed, and the topology of the myosin molecule with its associated light chains will be determined to establish models for regulation. The molecular basis of blood clotting is being studied by a similar approach. The structure of fibrinogen will be determined by X-ray crystallography and its packing established in the fibrin clot. These structural methods will also be applied to certain cytoskeletal and cell surface proteins (including those on human parasites) that play important roles in cell form, movement and interactions. The broad study of these systems is directed towards identifying distinctive features of structure that are essential to their function. Knowledge of the molecular mechanisms of contraction and its regulation in normal muscle is needed to account for their failure in various heart and muscle diseases. Similarly, a full understanding of blood clotting, and its malfunction in certain cardiovascular diseases, requires detailed information about the structure and interactions of the fibrinogen molecule. We now recognize the vital role of the cytoskelton and various arrays of internal and external cell surface proteins in normal cell function and in development, and the responsiveness of these structures to cell transformation. The occurrence of fibrous proteins that may be related to muscle proteins at the surface of pathogenic organisms has important medical implications. We believe that our broad study of the structure and interactions of these fibrous proteins will lead to a deeper understanding of both normal and abnormal cellular function.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Project (R01)
Project #
5R01AR017346-14
Application #
3154952
Study Section
Biophysics and Biophysical Chemistry B Study Section (BBCB)
Project Start
1974-09-01
Project End
1989-08-31
Budget Start
1986-09-01
Budget End
1987-08-31
Support Year
14
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Brandeis University
Department
Type
Schools of Arts and Sciences
DUNS #
616845814
City
Waltham
State
MA
Country
United States
Zip Code
02454
Gillilan, Richard E; Kumar, V S Senthil; O'Neall-Hennessey, Elizabeth et al. (2013) X-ray solution scattering of squid heavy meromyosin: strengthening the evidence for an ancient compact off state. PLoS One 8:e81994
O'Neall-Hennessey, Elizabeth; Reshetnikova, Ludmila; Senthil Kumar, V S et al. (2013) Purification, crystallization and preliminary X-ray crystallographic analysis of squid heavy meromyosin. Acta Crystallogr Sect F Struct Biol Cryst Commun 69:248-52
Brown, Jerry H (2013) Deriving how far structural information is transmitted through parallel homodimeric coiled-coils: a correlation analysis of helical staggers. Proteins 81:635-43
Kumar, V S Senthil; O'Neall-Hennessey, Elizabeth; Reshetnikova, Ludmila et al. (2011) Crystal structure of a phosphorylated light chain domain of scallop smooth-muscle myosin. Biophys J 101:2185-9
Brown, Jerry H; Kumar, V S Senthil; O'Neall-Hennessey, Elizabeth et al. (2011) Visualizing key hinges and a potential major source of compliance in the lever arm of myosin. Proc Natl Acad Sci U S A 108:114-9
Rosenbluth, Jack; Szent-Gyorgyi, Andrew G; Thompson, Joseph T (2010) The ultrastructure and contractile properties of a fast-acting, obliquely striated, myosin-regulated muscle: the funnel retractor of squids. J Exp Biol 213:2430-43
Brown, Jerry H (2010) How sequence directs bending in tropomyosin and other two-stranded alpha-helical coiled coils. Protein Sci 19:1366-75
Himmel, Daniel M; Mui, Suet; O'Neall-Hennessey, Elizabeth et al. (2009) The on-off switch in regulated myosins: different triggers but related mechanisms. J Mol Biol 394:496-505
Mentzer, Sarah E; Sundberg, John P; Awgulewitsch, Alexander et al. (2008) The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered Hoxc gene expression in the ears. Vet Dermatol 19:358-67
Brown, Jerry H; Yang, Yuting; Reshetnikova, Ludmilla et al. (2008) An unstable head-rod junction may promote folding into the compact off-state conformation of regulated myosins. J Mol Biol 375:1434-43

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