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A project‐oriented biochemistry laboratory for protein engineering and structure–function using small laccase enzyme from Streptomyces coelicolor.

Authors :
Van Wieren, Arie
Colen, Philip
Majumdar, Sudipta
Source :
Biochemistry & Molecular Biology Education; Nov2023, Vol. 51 Issue 6, p708-718, 11p
Publication Year :
2023

Abstract

An understanding of structure–function relationships in proteins is essential for modern biochemical studies. The integration of common freely accessible bioinformatics tools available online with the knowledge of protein‐engineering tools provide a fundamental understanding of the application of protein structure–function for biochemical research. In order for students to apply their prior knowledge of recombinant protein technology into the understanding of protein structure–function relationships, we developed a semester‐long project‐oriented biochemistry laboratory experience that is the second laboratory course of a series. For easier integration of knowledge and application, we organized this course into four sequential modules: protein structure visualization/modification, mutagenesis target identification, site‐directed mutagenesis, and mutant protein expression, purification, and characterization. These tasks were performed on the protein small laccase (SLAC) that was cloned and characterized by students in the previous semester during the first biochemistry laboratory course of the series. This goal‐oriented project‐based approach helped students apply their prior knowledge to newly introduced techniques to understand protein structure–function relationships in this research‐like laboratory setting. A student assessment before and after the course demonstrated an overall increase in learning and enthusiasm for this topic. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14708175
Volume :
51
Issue :
6
Database :
Complementary Index
Journal :
Biochemistry & Molecular Biology Education
Publication Type :
Academic Journal
Accession number :
173720380
Full Text :
https://doi.org/10.1002/bmb.21778