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. 2013 Jul 8;8(7):e66446. doi: 10.1371/journal.pone.0066446

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© 2013 Chen et al

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.

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(A) Comparisons of the transient declines in the protein synthesis rate and the intact EF2 concentration as modeled by the inhibition modes A ( = 0) and mode D ( = 0) of model V3 ( = 0.3 s⁻¹) in a control system ([R]_t = 0.5 µM and [EF2]_t = 0.6 µM). Insets show the same profiles in semi-log-linear scale. (B) A tenfold increase in [EF2]_t lengthens the latency for the onset of protein synthesis decline in the mode D, but accelerates the inhibition of protein synthesis more than EF2 inactivation in the mode A.

Inline graphic — (A) Comparisons of the transient declines in the protein synthesis rate and the intact EF2 concentration as modeled by the inhibition modes A ( = 0) and mode D ( = 0) of model V3 ( = 0.3 s⁻¹) in a control system ([R]_t = 0.5 µM and [EF2]_t = 0.6 µM). Insets show the same profiles in semi-log-linear scale. (B) A tenfold increase in [EF2]_t lengthens the latency for the onset of protein synthesis decline in the mode D, but accelerates the inhibition of protein synthesis more than EF2 inactivation in the mode A.