Individual
cells have the ability to perform complex mechanical tasks that
are essential for organism development and survival. For example,
single cells crawl or swim in the direction of external signals
during infection or embryogenesis, and groups of cells change shape
and coordinate movement to repair wounds or construct organs.
These dynamic
changes in cell morphology and location are mediated by the cytoskeleton,
a complex array of filaments and associated proteins that act as
the scaffold of cells. While many of the molecular components of
the cytoskeleton are well known, their collective interactions in
the form of a dynamic, adaptive mechanical system are not. Failures
in the regulation of the cytoskeleton can contribute to diseases
of the immune system and development, while engineering control
of cell movements could enable new biotechnologies that permit directed
drug delivery, promote tissue repair, or improve detection of infectious
agents.
The Fletcher
Lab studies the mechanics and dynamics of cell motility and shape
change on three levels:
- Purified proteins,
which are used for reconstitution and identification of minimal
systems for force generation, shape change, and spatial organization
- Whole cells, which
are used to investigate the ability of single cells to crawl,
swim, attach, and deform
- Groups of cells,
which are used to study aggregation and collective behavior
For these
studies, we are developing new instrumentation and measurement technologies
to quantify cell and molecular mechanics. Our tools include optical
microscopy, atomic force microscopy (AFM), optical trapping, and
microfabrication, as well as biophysical modeling and simulation.
Based on our understanding of cell and molecular mechanics, we are
developing medical devices that aid in clinical diagnosis and treatment
of disease.
Major support:
NSF (BES), NIH (NIGMS), DOE (LBL, LLNL), NCIIA, CRCC |
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