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Martin Muschol,
Assistant Professor
Ph.D. physics, 1992 City University of New York
office:
PHY102A
(813) 974-2564
lab: PHY102B/C
(813) 974-9827
e-mail:
mmuschol@cas.usf.edu

research interests: optical methods in biological physics
● Imaging Neuronal Activity
● Modeling Neuronal Information
Processing
● Optical Detection of Protein
Interactions and Aggregation
● Colloidal Models of Protein
Interactions
● New Optical Techniques for
Biological Physics
research outline:
Short-Term Plastic Changes in Neurons:
One fundamental property of neurons is their "plasticity", i.e.
their ability to change their response after repeated stimulation.
This ability is thought to underlie such essential processes as
learning and memory formation. We are using high-speed optical
recording techniques to monitor stimulation-induced changes in
electrical activity and the spatio-temporal patterns of calcium
levels in the axons and nerve terminals of hypothalamic neurons.
Using these optical data and simplified computational models, we are
trying to unravel the cellular and sub-cellular mechanisms giving
rise to neuronal plasticity at the presynaptic level.
Colloidal Models of Protein Aggregation:
Proteins in solutions frequently form disordered precipitates. We
have shown previously that colloidal models of protein interactions
can provide valuable insights into the ubiquitous tendency of
proteins to aggregate. We are now investigating if and how these
colloidal models can help us understand protein aggregation that
occurs in neurodegenerative diseases like Alzheimer's or Parkinson
disease. To do so, we are using advanced optical techniques to
follow the kinetics of protein aggregation. We then compare our
experimental observations with predictions of colloidal models for
the phase behavior of proteins in solution.
Curriculum Vitae
additional info:
Optical Recording of
Electrical Activity in the Posterior Pituitary Gland:
The four images
below display an optical recording of the voltage signal (action
potential) invading the posterior pituitary gland after in response
to a single stimulus. A large bundle of axons form the hypothalamus
enters the posterior pituitary gland (at the top of the image) and
arborizes extensively within the gland. The pituitary gland was
stained with a voltage-sensitive dye and the axons entering the
gland were stimulated with a bipolar electrode (located at the top,
just outside the view field). These four fluorescence images show
the changes in fluorescence intensity induced by the propagation of
the compound action potential (i.e. the electrical excitation wave)
through the gland in response to a single stimulus. This sequence
cover a time span of only 10 ms.

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