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. Author manuscript; available in PMC: 2010 Oct 1.
Published in final edited form as: Proteins. 2009 Oct;77(1):62–73. doi: 10.1002/prot.22417

Figure 1.

Figure 1

Protocols for the experiments: (a) The cooling experiment. (1) text (extraction time) to remove samples from the heater at 65±2°C and pH 1.6 (1.5 h was the time chosen). (2) Δtcool (cooling time at 25±2°C and pH 1.6) for different times up to 28 days, and (3) trepl (replacement time) to replace the cooler samples into 65±2°C and pH 1.6. For graph (i), the standard kinetic curve (Inline graphic) was obtained by fitting Eq. (2) to averaged data from twelve different runs. The values of the parameters from the model fit using Eq. (2) were: tlag = 3.47 h, t50 = 4 h, kapp = 3.76 h-1 (R2=0.983). For graph (ii), we used averaged data for the standard kinetic experiment (◆) and for cooled and re-heated samples (Inline graphic). (b) The seeding experiment. (1) Left figure: text,olig/fiber (extraction time for oligomer or fiber) is the time at which samples are removed from a run at 65±2°C and pH 1.6, and (2) Right figure: sigmoidal curves with and without seeds. Averaged data were used for the standard kinetic experiment (◆) and for a seeded run (Inline graphic). Model fits using Eq. (2) (Inline graphic).