Tatiana G Shapkina
Raleigh, NC 27604
919-***-**** (home)
919-***-**** (cell)
acckq1@r.postjobfree.com
SUMMARY
Highly experienced biochemist with more than twenty years of research lab expertise,
looking for an opportunity to contribute to biotech industry.
Proficient in wide variety of laboratory techniques including: ribosomes, nucleic acids
and tagged and untagged protein purification; radioactive and fluorescent labeling; preparative
and analytical gel electrophoresis, LC, HPLC, ultracentrifugation, PCR; data analysis using
Excel and Kaleidagraph programs. Familiar with stopped-flow and quench-flow techniques,
fluorescence polarization method, Alpha-screen, LANCE.
EXPERIENCE
NC State University – Raleigh, NC September 1996 – August 2013
Department of Molecular and Structural Biochemistry, Laboratory of Professor P. Wollenzien
Research Specialist
• Involved in numerous projects investigating the structure and structure-function
relationship of bacterial ribosomes and ribosomal ligands using various biochemical
approaches such as UV-crosslinking, foot- and toe-printing, filter-binding assay, kinetic
and thermodynamic studies of complex formation by rapid quenching and stopped flow
methods.
• Purified multiple protein factors and substrates of protein synthesis machinery for use in
laboratory experiments.
• Participated in assay development and implementation for small biotech companies:
High Throughput Screening of chemical compounds as inhibitors of protein synthesis
in Staphylococcus aureus (TRANA Discovery, Inc., Cary, NC).
This involved setting up and testing assays with Escherichia Coli and Staphylococcus
aureus ribosomes using ALPHA-screen, LANCE and fluorescence polarization
systems.
Biochemical characterization and determination of specific sites of action of
compounds selected by the above mentioned HTS and analysis of their footprints on
Staphylococcus aureus ribosomes.
Assessment of DNA– lipoprotein complex formation (ALERA Labs, LLC., Research
Triangle Park, NC).
Developed fluorescence anisotropy assay and used it to analyze interaction of DNA-
oligo with proprietary lipoprotein in aqueous solutions.
• Performed lab manager duties such as overseeing safety, radiation inventory and
personnel training, ordering, and equipment maintenance.
• Trained undergraduate and graduate students in sample preparation and analytical
methods.
Nuclear Physics Institute – St. Petersburg Russia June 1995 – August 1996
Department of Molecular and Radiation Biophysics, Laboratory of Protein Synthesis
Scientist
• Finished work on and defended doctoral dissertation “Puromycin reaction of A-site
bound peptidyl-tRNA”
• Participated in a large scale preparation of individual tRNAs for commercial use.
North Carolina State University – Raleigh, NC June 1992 – May 1995
Department of Molecular and Structural Biochemistry, Laboratory of Professor P. Wollenzien
Visiting Scientist
• Studied the structure of mRNA-70S ribosomal complexes by UV-crosslinking of s 4U-
labeled mRNA and rRNA.
Leningrad Nuclear Physics Institute – Russia September 1983 – May 1992
Department of Molecular and Radiation Biophysics, Laboratory of Protein Synthesis
Junior Scientist April 1985 – May 1992
• Purified and labeled individual tRNAs for the laboratory use.
• Studied interaction of tRNAs with bacterial ribosomes.
Intern September 1983 – March 1985
• Learned laboratory techniques, studied interaction of tRNAs with mammalian ribosomes.
EDUCATION
Engelhardt Institute of Molecular Biology – Moscow, Russia February 1995
PhD, Molecular Biology
Leningrad Polytechnical Institute – Leningrad, Russia February 1985
(now St.Petersburg State Polytechnical University)
BS/MS, Biophysics – Department of Physics and Mechanics
Master of Science theses “Interaction of deacylated tRNA with rat liver ribosomes.”