Fragment-Based Ligand Discovery Using Protein-Observed 19F NMR: A Second Semester Organic Chemistry CURE Project

被引:9
作者
Bur, Scott K. [2 ]
Pomerantz, William C. K. [1 ]
Bade, Morgan L. [2 ]
Gee, Clifford T. [1 ]
机构
[1] Univ Minnesota, Dept Chem, Minneapolis, MN 55455 USA
[2] Gustavus Adolphus Coll, Dept Chem, St Peter, MN 56028 USA
基金
美国国家科学基金会;
关键词
Laboratory Instruction; Organic Chemistry; Inquiry-Based/Discovery Learning; NMR Spectroscopy; Proteins/Peptides; RESEARCH EXPERIENCES; SCIFINDER SCHOLAR; HOT-SPOTS; INHIBITOR; BENEFITS; DESIGN; MOTIFS; FAMILY; DOMAIN;
D O I
10.1021/acs.jchemed.1c00028
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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 F-19 (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 K-d 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 secondsemester organic chemistry laboratory course, a PrOF NMR fragment-based ligand discovery lab can be readily implemented in the undergraduate chemistry curriculum.
引用
收藏
页码:1963 / 1973
页数:11
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