کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2188777 | 1096185 | 2007 | 5 صفحه PDF | دانلود رایگان |

The formation of polypeptide aggregates, including amyloid fibrils and prions, is a biochemical process of considerable interest in the context of its association with ageing and neurodegeneration. Aggregation occurs typically with a lag phase and a growth phase that reflect an underlying nucleation-polymerisation mechanism. While the propensity of nucleation can be estimated from the lag time tl, the efficiency of growth is represented by the growth rate kg. Here, I have analysed the absolute kg and tl values from a total of 298 samples prepared from insulin, glucagon and different sequence variants of the Alzheimer's Aβ(1-40) peptide. Although these samples differ in the conditions of aggregation, systematic comparison reveals an overall similarity in the plot of kgversus tl. The plot fits readily with the simple equation kg = α/tl and by using a proportionality factor α of 4.5. In contrast to the individual values of kg and tl that depend substantially on sequential and environmental parameters, α seems much less affected by such factors. These data suggest mechanistic similarities in the nucleation behaviour of different amyloid-like fibrils and aggregates.
Journal: Journal of Molecular Biology - Volume 365, Issue 5, 2 February 2007, Pages 1266–1270