The Effect of Osmolytes on Protein Fibrillation

被引:70
|
作者
Macchi, Francesca [1 ]
Eisenkolb, Maike [2 ]
Kiefer, Hans [2 ]
Otzen, Daniel E. [1 ]
机构
[1] Aarhus Univ, iNANO, Ctr Insoluble Prot Struct inSPIN, Dept Mol Biol & Genet, DK-8000 Aarhus C, Denmark
[2] Hsch Biberach, Pharmaceut Biotechnol, D-88400 Biberach, Germany
关键词
glucagon; amyloid; taurine; polymorphism; fibrillation mechanism; TRIMETHYLAMINE-N-OXIDE; THIOFLAVIN T FLUORESCENCE; ALPHA-SYNUCLEIN; IN-VITRO; GLUCAGON FIBRILLATION; INHIBITS AGGREGATION; CHEMICAL CHAPERONES; THERMAL-STABILITY; PRION PROTEIN; GIBBS ENERGY;
D O I
10.3390/ijms13033801
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Osmolytes are small molecules that are exploited by cells as a protective system against stress conditions. They favour compact protein states which makes them stabilize globular proteins in vitro and promote folding. Conversely, this preference for compact states promotes aggregation of unstructured proteins. Here we combine a brief review of the effect of osmolytes on protein fibrillation with a report of the effect of osmolytes on the unstructured peptide hormone glucagon. Our results show that osmolytes either accelerate the fibrillation kinetics or leave them unaffected, with the exception of the osmolyte taurine. Furthermore, the osmolytes that affected the shape of the fibrillation time profile led to fibrils with different structure as revealed by CD. The structural changes induced by Pro, Ser and choline-O-sulfate could be due to specific osmolytes binding to the peptides, stabilizing an otherwise labile fibrillation intermediate.
引用
收藏
页码:3801 / 3819
页数:19
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