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. Author manuscript; available in PMC: 2019 May 31.
Published in final edited form as: J Phys Chem B. 2018 Mar 9;122(21):5567–5578. doi: 10.1021/acs.jpcb.7b11830

Figure 3.

Figure 3

(left) Bound state lifetimes (computed from Eq. (6) and Eq. (14)) as a function of the alignment between the incoming molecule and the fibril. The lifetime is maximized in the perfectly aligned state (R = 0) and drops exponentially as |R| increases. (right) Capture probabilities (Eq. (18)) of the uniform sequence as a function of the alignment. As the concentration increases, the rate of monomer collisions with the fibril end increases from ron=104 s−1 (black), 106 s−1 (red), to 108 s−1 (blue). The capture probability transitions from a sharply peaked function at R = 0 to a broad plateau. The plateau indicates that many mis-registered molecules are incorporated in the fibril. ε0 = 0.5, L = 20