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. 2012 Mar 24;40(6):2807–2821. doi: 10.1093/nar/gks214

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© The Author(s) 2012. Published by Oxford University Press.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Figure 8. — Comparison of the experimental dependencies of EC₅₀ on C_KCl (data of DLS and PA shown as points with thin lines) to the calculated values using Equation (3) (displayed as smooth thick lines). (A–C) Results obtained for ε-oligolysine homologues from εK5 to εK10. Theoretical curves were drawn as follows: (A) fixed value N_crit = 0.88 and the best fit values SK = 0.85Z and K_d(1 M) = 0.33 (eK5), 0.22 M (eK10) are used. Theoretical curves in (B) and (C) were built without fitting using the values SK = 0.85Z and K_d(1M) = 0.22 M; (B). Data for εK6 and εK9; (C) data for εK7 and εK8. (D) Comparison of the results calculated with Equation (3) with experimental results of the DLS and PA methods of εK10 and εLK10. Best fit is for K_d(1M) = 18 M and SK = 0.85Z with the fixed value N_crit = 0.88; the data for εK10 are the same as in (A). See text for details.