RESEARCH
Current Funding: National Institutes of Health
Project Title: Inositol
Isomer Transport Kinetics and Utilization
Duration:
Principal Investigator: Phillip E. Ryals,
Ph.D.
Description: The
importance in eukaryotes of polyphospho-myo-inositides
and polyphospho-myo-inositols in mediating
cellular responses to specific extracellular signals
is well established. In addition, myo-inositol is found in other important, more
complex molecules such as glycosyl phosphatidyl (GPI)-anchored proteins, where it may also
participate in signaling cascades. It is
becoming increasingly apparent that non-myo-inositol-containing,
isomeric phosphoinositides are more common than once
believed, with (1D)chiro-
and/or scyllo-inositol-containing phosphatidylinositols having been reported in mammals,
plants, and a lower eukaryote. Given the
importance of understanding the potential of non-myo-inositol-containing
lipids and second messengers in transmembrane and
intracellular signaling, it is imperative to examine the biochemistry of these
molecules. Using the technique of radioisotopic labeling in conjunction with kinetic
analyses, chromatography, electrophoresis, and other methods, the applicant
will (1) characterize the transport kinetics of three inositol
isomers, (2) examine the utilization of these isomers in the biosynthesis of phosphoinositides, phosphoinositols,
and GPI-anchored proteins, (3) characterize the utilization of inositol isomers by phosphatidylinositol
synthase, and (4) determine the susceptibility of
non-myo-inositol-containing phosphatidylinositol to degradation by seven common phospholipases. By
understanding the basic mechanisms of inositol isomer
uptake, utilization, biosynthesis, and degradation, the foundation is laid for
accomplishing the long term goals of this project, which include an examination
of the structure/function relationships among the isomeric inositol
lipids, the influence these lipids exert on the biophysical properties of membranes,
and the role non-myo-inositol second
messengers play in signaling cascades.
Current Funding: Merck/AAAS
Undergraduate Interdisciplinary Research Program
Duration: 05/04
– 05/10
Principal Investigators: T. Fox, P. Ryals, V. Sharma (Department
of Biology)
M.
Huggins, T. Royappa, T. Sirvent
(Department of Chemistry)
Description: Funding is provided for 3 separate research projects. Each project represents a collaborative
effort directed by a pair of principal investigators from the Biology and
Chemistry departments. A total of 6
undergraduates participate each year. Matching
funds provided by the