NPB Neurobiology, Physiology & Behavior

Samantha Harris
Assistant Professor
189 Briggs Hall
Office: 530.752.0642
Lab: 530.754.9860
samharris (at) ucdavis (dot) edu
Lab web page

Degrees:
B.S., University of Illinois, 1988
PhD., University of Michigan, 1995

Awards:
American Heart Association New Investigator Award, 2003
American Heart Association McClain Research Award, 2002
American Heart Association Chippewa Valley Research Award, 1998
American Physiological Society Caroline tum Suden Professional Opportunity Award for Meritorious Research, 1993


Research Interests:
Research in my lab is focused on understanding the molecular mechanisms of cardiac contraction and the role contractile proteins play in inherited cardiomyopathies and heart failure. Muscle contraction, including contraction of the heart, occurs as the result of cyclic interactions between myosin and actin, two of the major contractile proteins found in muscle. Numerous other contractile proteins also contribute to contraction and help determine the force and speed of contraction, factors which in turn affect the strength and speed at which the heart pumps blood. Recent discoveries show that many instances of heart disease, including many instances of sudden death in otherwise young, healthy individuals, are due to defects in contractile proteins. Multiple, distinct defects in over 10 different contractile proteins have been identified that together account for a wide spectrum of disease symptoms from very mild to sudden death. Understanding how these numerous contractile proteins work together to produce force and how defects in them can ultimately lead to disease is the central research interest of my lab.

To pursue these research questions we employ a combination of genetic, molecular, biochemical, and biophysical approaches. In particular, we’ve used gene targeting techniques to “knockout” or alter specific myofilament proteins. Structural and functional deficits produced by these genetic manipulations are then assessed using a variety of echocardiographic, histological and ultrastructural imaging, and northern and western blotting methods. Mechanical force measurements, including measurements of shortening velocity, rate of activation, and isometric tension are utilized to determine the functional effects of mutations on force in individual heart cells. Results from these studies provide a better understanding of the molecular mechanisms of muscle contraction and how defects in contractile proteins can cause altered heart function and ultimately lead to disease.

Selected Publications:
C.M. Jeffries, A.E. Whitten, S.P. Harris, and J. Trewhella. Small-Angle X-ray Scattering Reveals the N-Terminal Domain Organization of Cardiac Myosin Binding Protein C. J Mol Biol., Feb 4, 2008. [Epub ahead of print]

R.W. Kensler and S.P. Harris. The Structure of Isolated Myosin Thick Filaments from cMyBP-C Knockout Mice. Biophys J, Mar 1;94(5):1707-18, 2008. [Epub 2007 Nov 9]

J.F. Shaffer, M. Razumova, A-Y Tu, M. Regnier, and S.P. Harris. Myosin S2 is Not Required for Effects of Myosin Binding Protein-C on Motility. FEBS Letters, 581: 1501-1504, 2007.

M. Razumova, J. Shaffer, A.Y. Tu, G. Flint, M. Regnier, and S.P.Harris. Effects of the N-Terminal Domains of Myosin Binding Protein-C in an In Vitro Motility Assay: Evidence for Long-Lived Cross-Bridges. Journal of Biological Chemistry, 281:35846-35854, 2006.

S.P. Harris, E. Rostkova, M. Gautel, and R.L. Moss. Binding of Myosin Binding Protein-C to Myosin Subfragment S2 Affects Contractility Independent of a Tether Mechanism. Circulation Research, 95:930-936, 2004.

S.P. Harris, E. Rostkova, M. Gautel, and R.L. Moss. Binding of Myosin Binding Protein-C to Myosin Subfragment S2 Affects Contractility Independent of a Tether Mechanism. Circulation Research, In press, 2004.

B.M. Palmer, D. Georgakopoulos, P.M. Janssen, Y. Wuang, D.F. Belardi, P.G. Burgon, C.E. Seidman, J.G. Seidman, S.P. Harris, R.L. Moss, N.R. Alpert, D.W. Maughan, and D.A. Kass. Role of Cardiac Myosin Binding Protein C in Sustaining Left Ventricular Systolic Stiffening. Circulation Research, 94:1249-55, 2004.

F.S. Korte, K.S. McDonald, S.P. Harris, and R.L. Moss. Loaded Shortening, Power Output, and Rate of Force Redevelopment are Increased with Knockout of Cardiac Myosin Binding Protein-C. Circulation Research, 93:752-758, 2003.

S.P. Harris, W.T. Heller, M.L. Greaser, R.L. Moss, and J. Trewhella. Solution Structure of Heavy Meromyosin by Small-Angle Scattering. Journal of Biological Chemistry, 278:6034-6040, 2003.

S.P. Harris, C.R. Bartley, T.A. Hacker, K.S. McDonald, P.S. Douglas, M.L. Greaser, P.A. Powers, and R.L. Moss. Hypertrophic Cardiomyopathy in Cardiac Myosin Binding Protein-C (cMyBP-C) Knockout Mice. Circulation Research, 90:594-601, 2002.

S.P. Harris, J.R. Patel, L.J. Marton, and R.L. Moss. Polyamines Decrease Ca2+ Sensitivity of Tension and Increase Rates of Tension Development in Skinned Cardiac Myocytes. American Journal of Physiology 279: H1383-1391, 2000.