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Contact Info

James L. McGrath, Ph.D. Department of Biomedical Engineering University of Rochester work Box 270168 Rochester, NY 14627-0168 office: Goergen Hall 306 p 585-273-5489 f 585-273-4746 McGrath

Recent Publications

  • (2014 Jul). Highly porous silicon membranes fabricated from silicon nitride/silicon stacks. - Small (Weinheim an der Bergstrasse, Germany).
    • Chung HH
    • Chan CK
    • Khire TS
    • Marsh GA
    • Clark A
    • Waugh RE
    • McGrath JL
    (2014 Jun 17). Highly permeable silicon membranes for shear free chemotaxis and rapid cell labeling. - Lab on a chip.
  • (2013 Dec). Dynamics of adhesion molecule domains on neutrophil membranes: surfing the dynamic cell topography. - European biophysics journal : EBJ.
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Graduate Students

James L. McGrath

  • Ph.D., Harvard–MIT, 1998
Photo of James McGrath
  • Professor

    • Biomedical Engineering

McGrath Lab

Research Overview

Our laboratory maintains research programs in three areas:

  1. The study of molecular and physical mechanisms in cell migration

    We are seeking a mechanistic understanding of the collective cell migration exhibited by endothelial cells as well as the ameboid-like migration of leukocytes. In this work we are developing predictive mathematical models by using quantitative microscopy to determine key model parameters and to test model predictions.

  2. The characterization of nanoparticle interactions with protein and cellular systems

    We are pioneering methods for relating the physical properties of nanoparticles to their capacity for protein binding and to their fate within cells. The goal of this work is to understand the characteristics that make nanoparticles toxic in some cases and effective as probes or delivery vehicles in other instances. These first two research programs rely heavily on our ever-growing repertoire of microscope-based techniques for the quantitatively characterization of living cells.

  3. The development of ultrathin silicon nanomembranes for biological applications

    We are advancing a research program in a broad effort to revolutionize silicon-based membrane material discovered at the University of Rochester. The freestanding, nanoporous membrane material is also molecularly thin and mechanically robust. We have shown that it can be used for size and charge-based separation of proteins and other biomolecules at rates orders-of- magnitude faster than traditional membrane materials. The membranes are also transparent and fully biocompatible so that cells of different types can be grown on either side of the membrane to remain separated by a molecularly thin, porous layer. By developing the membrane material as a cell culture substrate, we are helping biomedical scientists and developmental biologists address long- standing questions about short distance cell-cell communication. more info...