Samy Morris Samy, Ph.D.
Post-Doctoral Fellow

Contact Information:
Department of Biochemistry and Molecular Biology
Michigan State University
East Lansing, MI 48824-1319
samys@pilot.msu.edu

Education & Work Experience

1997-2000 Bio products laboratory, UK

1992-1997: Ph.D. Birkbeck College
University of London, UK

1990-1991: M.Sc. Department of Biology
University College London, UK

1989-1990: Postgraduate diploma
London School of Hygiene and Tropical Medicine, London, UK

1979-1983: B.Sc. (Hons)Ain Shames University
Cairo, Egypt

Interest and work experience

Work at Bio products laboratory involved purification, characterization, formulation and stability of monoclonal and recombinant anti-bodies. Solving problems and validating assays regarding IEF/SDS capillary electrophoresis. Glycan structure analysis, optimizing the peptide mapping of the Monoclonal antibodies. Involvement in PLA compilation and submission to ICH (EMEA/FDA) standards. Designed and performed various method validations for a number of techniques. Performance verification and operational qualification of various equipment. Experience in GLP, GMP, and SLP working practices

The Ph.D. project involved collaboration between the University of London and the Institute of Food Research at Reading University. The overall aim of the project was to investigate the thermo stability and the pH stability of Chymosin and other aspartic proteinase enzymes; this was involving both molecular biology and biochemical investigation through a fungal expression system. In addition, a variety of specific mutations have been introduced into the Chymosin gene.

The objective of my postdoctoral work is to have a clear idea regarding the structure of the hERaLBD. Currently, Dr. Zacharewski employs studies that are able to monitor the estrogenic potency of chemicals by their ability to bind the human estrogen receptor (hER) and cause upregulation of an engineered reporter gene construct. These studies are very specific for monitoring chemicals that will bind the human receptor. The study involve expression, purification and crystallization of the hERaLBD. The work also involves investigation of the effect of gestational and lactational exposure to estrogenic chemicals (i.e. estrogenic endocrine disrupters) on testicular gene expression and spermatogenesis in mice. This project test the hypothesis that exposure to endocrine disrupters during development compromises male fertility as a result of alterations in testicular gene expression profiles, sperm assessment. This investigated through in vitro fertilization, in situ hybridization, cDNA array technology, bioinformatics and the statistical analysis of gene expression data.




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