Graduate NIH Training in BiotechnologyTraineesAndrew Kim Project Description Protein aggregation is the chief mode of product degradation in the bioprocessing of therapeutic drugs and can lead to reduced bioactivity and altered immunogenicity. The weak protein interactions that lead to aggregation are quantified by the osmotic second virial coefficient (B22) which can be measured by using a novel technique, self-interaction chromatography (SIC). We plan to use SIC, in conjunction with site-directed mutagenesis and modeling, to develop a rational high-throughput screening method for formulations that minimize protein aggregation. To enable parallel experimentation, we will design and fabricate a miniaturized SIC device. Courses Foundations Course (2005) Molecular Biophysics I Molecular Biophysics II Scientific Ethics Placed out of Fundamentals of Biochem E Physical Biochemistry Advanced Thermodynamics Advanced Fluid Mechanics Publications None Presentations Chemical Engineering Graduate Student Association Symposium 2006 - Carnegie Mellon University - Poster presentation Seminars CMU Chemical Engineering, CMU Biomedical Engineering
Advisor Todd Przybycien Carnegie Mellon University |
Biotechnology Program
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