insulin;
protein aggregation;
amyloids;
nucleation;
Thioflavin T;
fluorescence;
D O I:
10.1110/ps.051692305
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:
When subjected to acidic conditions and high temperature, insulin is known to produce fibrils that display the common properties of disease amyloids. Thus, clarifying the mechanisms of insulin fibrillation can help the general understanding of amyloidal aggregation. Insulin fibrillation exhibits a very sharp time dependence, with a pronounced lag phase and subsequent explosive growth of amyloidal aggregates. Here we show that the initial stages of this process can be well described by exponential growth of the fibrillated proteins. This indicates that the process is mainly controlled by a secondary nucleation pathway.
机构:
Univ London Imperial Coll Sci Technol & Med, Sch Med St Marys, MRC, Prion Unit, London, EnglandUniv London Imperial Coll Sci Technol & Med, Sch Med St Marys, MRC, Prion Unit, London, England
机构:
Univ London Imperial Coll Sci Technol & Med, Sch Med St Marys, MRC, Prion Unit, London, EnglandUniv London Imperial Coll Sci Technol & Med, Sch Med St Marys, MRC, Prion Unit, London, England