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Atomic Force Microscopy for Physiological Studies at the Nano Scale
Sat. April 1—1:00-3:00 PM
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| Chaired: |
Gerald A. Meininger, Texas A&M
Univ. Hlth. Sci. Ctr.
Michael J. Davis, Texas A&M Univ. Hlth. Sci. Ctr. |
A major barrier to the advancement of scientific
understanding in a field is intimately tied to technical limitations. Thus,
important new advances are frequently catalyzed by the introduction of new
technology into a field. Developments in the use of Atomic Force Microscopy
for biological studies represents an example of how a new technology is
stimulating advances in microscopy, understanding cell and subcellular
mechanical properties, cell signaling, molecular sensing and recognition.
This workshop will include an introduction and four presentationsby
recognized experts in the field that will highlight application of atomic
force microscopy to address questions of relevance to physiologists and cell
biologists. The presentations will be designed to provide the audience with
an overview of the general theory and principles of operation behind atomic
force microscopy followed by specific examples of how this technology can be
used.
Our principal aim in this workshop is to
highlight several applications of atomic force microscopy that cover studies
of cell mechanical properties and responses to mechanical responses,
cell-cell adhesive interactions, cell-protein (receptor-ligand)
interactions, and molecular recognition imaging.
The workshop will include an introduction that
highlights the history of Atomic Force Microscopy and its use in
experimental biology and medicine and presents the conceptual format the
areas to be covered by the various speakers. The first speaker will be Dr.
Peter Hinterdorfer, a recognized leader in the field of molecular
recognition imaging. Molecular recognition imaging provides insights into
the dynamics of the receptor-ligand recognition process and gives
investigators information about the nature of binding sites, binding energy
barriers, and the kinetics of reactions. Applications of this approach are
useful for study of isolated proteins, native membranes, viruses, and intact
cells. The second speaker will be Dr. Michael Horton who has been a major
proponent of the use of atomic force microscopy to probe the mechanical
properties of osteoblasts and the responses of osteoblasts to applied
mechanical forces. He has been a pioneer in the hybridization of atomic
force microscopy with confocal microscopy for fluorescence studies in order
to simultaneously combine measurements made with the atomic force microscope
with fluorescent signals relevant to cell signaling. The third speaker will
be Dr. Andreea Trache, an optical physicist with biophysics expertise, who
will discuss a unique atomic force-multioptical imaging integrated
microscope that she has designed for studies of vascular cell
mechanotransduction, extracellular matrix-integrin interactions and focal
contact remodeling in response to applied mechanical force. The fourth and
last speaker will be Dr. Vincent Moy who has expertise using the atomic
force microscope to characterize the mechanical properties of receptor-ligand
interactions as a function of the mechanical loading rate and has adapted
his approaches to permit studies of white cell-endothelial cell adhesive
interactions using intact cells.
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1:00 PM |
Chairman’s
introduction.
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1:20 PM |
Molecular recognition force microscopy for detection
and recognition of single Molecules
Peter Hinterdorfer, Johannes Kepler Univesity of Linz
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1:40 PM |
Single cell mechanotransduction and modulation in bone
cells: approaches combing atomic force microscopy and confocal
microscopy
Andrew Pelling, Univ. Col. London
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2:00 PM |
An atomic
force-multi-optical imaging integrated microscope for monitoring
vascular cell responses to mechanical forces and focal contact
remodeling.
Andreea Trache, Texas A&M Univ.
Hlth. Sci. Ctr.
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2:20 PM |
Atomic force microscopy: A tool for
studies of molecular and cell adhesion and cell mechanics
Vincent T. Moy, Univ. of Miami
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2:40 PM |
General discussion. |
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