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Fragment-Based Ligand Discovery Using Protein-Observed 19F NMR: A Second Semester Organic Chemistry CURE Project.
Bur, Scott K; Pomerantz, William C K; Bade, Morgan L; Gee, Clifford T.
Affiliation
  • Bur SK; Department of Chemistry, Gustavus Adolphus College, St. Peter, Minnesota 56028, United States.
  • Pomerantz WCK; Department of Chemistry, University of Minnesota, Minneapolis, Minnesota 55455, United States.
  • Bade ML; Department of Chemistry, Gustavus Adolphus College, St. Peter, Minnesota 56028, United States.
  • Gee CT; Department of Chemistry, University of Minnesota, Minneapolis, Minnesota 55455, United States.
J Chem Educ ; 98(6): 1963-1973, 2021 Jun 08.
Article in En | MEDLINE | ID: mdl-37274366
Curriculum-based undergraduate research experiences (CUREs) have been shown to increase student retention in STEM fields and are starting to become more widely adopted in chemistry curricula. Here we describe a 10-week CURE that is suitable for a second-semester organic chemistry laboratory course. Students synthesize small molecules and use protein-observed 19F (PrOF) NMR to assess the small molecule's binding affinity to a target protein. The research project introduced students to multistep organic synthesis, structure-activity relationship studies, quantitative biophysical measurements (measuring Kd from PrOF NMR experiments), and scientific literacy. Docking experiments could be added to help students understand how changes in a ligand structure may affect binding to a protein. Assessment using the CURE survey indicates self-perceived skill gains from the course that exceed gains measured in a traditional and an inquiry-based laboratory experience. Given the speed of the binding experiment and the alignment of the synthetic methods with a second-semester organic chemistry laboratory course, a PrOF NMR fragment-based ligand discovery lab can be readily implemented in the undergraduate chemistry curriculum.
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