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Structural Basis of Motility

Cryo-Electron Microscopy


Understanding biological function requires knowledge of the three-dimensional structures of the macromolecular complexes that power the cell. Recent, revolutionary advances in cryo-electron microscopy make it possible to observe protein structure at near-atomic resolution, both in purified complexes and in the cell. We use cryo-EM (together with other EM and X-ray diffraction techniques) to determine the structures of the protein molecules of muscle, and the higher order complexes that they form, in different functional states. We make use of the superbly equipped cryo-EM Core at UMass Medical School (Massachusetts Facility for High-resolution Cryo-electron Microscopy) to carry out this work.

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Research Focus


Cryo-EM Studies Elucidate Motor Protein Function

Movement is a defining feature of life. Our goal is to understand how muscles contract to move the body, and how cells move and change shape. We use cryo-electron microscopy and image analysis to study the structure of the motor proteins and filaments that underlie these movements. We are especially interested in the molecular switches that turn contraction and motility on and off. We study skeletal, cardiac, smooth and nonmuscle cells, and complement this work with low-angle X-ray diffraction of muscle and solution biophysical techniques. Our studies provide a structural basis for understanding diseases that result from mutations in contractile proteins.

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