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Department of Biology |
Joseph McCray
Department of Biology
Associate
Professor
B.S.: Biology, General Biology (Honors) (BIO 111-112 Honors Senior Seminar in Biology (BIO 425) Immunochemistry The major project in the laboratory involves studies of the cell
surface receptor binding sites of rhinoviruses, a major cause of the common
cold, using anti-peptide antibodies. Polyclonal and monoclonal antibodies
against two synthetic peptides related to this site have been prepared,
purified, and characterized. At present, the study of the specific
characteristics of these antipeptide antibodies is being continued and study
of their ability to neutralize infectivity of rhinoviruses in in vitro
systems is being initiated. In addition, in collaboration with Dr. Paul
Knopf's research group at Abstracts Petzke, M.M., P.K. Suri, M. Goldberg,
S.F. Taylor, S. Ranji, H. Taylor, J.W. McCray, Jr. and P.M. Knopf. 1999.
Evidence of alternative antigenic conformations of an epitope of Sm25, a
tegumental protein of Schistosoma mansoni. (under revision) Suri, P.K., M. Goldberg, B. Chakraborty,
K.B. Nguyen, R. Bungiro, Jr., M. Madikisela, M.M. Petzke, S. J. Davies, J.W.
McCray, Jr. and P.M. Knopf. 1997. Evaluation of recombinant protein r140, a
polypeptide segment of tegumental glycoprotein Sm25, As a defined antigen
vaccine against Schistosoma mansoni. Parasite Immunology 19: 5515-1529 Aschauer, B., G, Werner, J. McCray, B. Rosenwirth,
and H. Bachmayer. 1991. Biologically active protease 3C of human rhinovirus
IA is expressed from a cloned cDNA segment in Escherichia coli.
Virology, 184: 587-594. To the Morehouse College Homepage Department of Biology Office: 322
Nabrit-Mapp-McBay Science Building (404) 215-2609 Last Updated:
Aug. 25, 03 / Porsch R. Fallen |