Spectroscopic Characterization of Amyloid Fibril Formation by Lysozyme

被引:9
作者
Myers, Jeffrey K. [1 ]
机构
[1] Davidson Coll, Dept Chem, Davidson, NC 28035 USA
关键词
Upper-Division Undergraduate; Biochemistry; Laboratory Instruction; Hands-On Learning/Manipulatives; Inquiry-Based/Discovery Learning; Biophysical Chemistry; Conformational Analysis; Enzymes; Proteins/Peptides; Spectroscopy; EGG-WHITE LYSOZYME; CIRCULAR-DICHROISM; CONGO RED; PROTEINS; CRYSTAL;
D O I
10.1021/ed400400x
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hen egg white lysozyme is used as a model protein to study amyloid fibril formation (fibrillation). This three-week laboratory experience has been successfully implemented in an upper-level biochemistry course to introduce students to issues of protein conformation, spectroscopic characterization of conformational changes, and misfolding of proteins related to disease. The fluorescence and absorbance of amyloid-specific dyes are used to detect fibrillation; accompanying changes in secondary structure are revealed by circular dichroism. Potential small molecule fibrillation inhibitors are tested, and kinetics experiments are carried out to probe the effect of seeding with preformed fibrils on the rate of fibrillation.
引用
收藏
页码:730 / 733
页数:4
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