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. 2012 Mar 30;7(3):e33441. doi: 10.1371/journal.pone.0033441

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Magnus and Regoes.

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) The relative infectivity is shown as a function of the fractions of envelope proteins defective of function A, , and the fraction of envelope proteins defective of function B, . The grey plane shows the predictions for a model in which the two functional units A and B are located on the same envelope protein, the blue plane the model in which these function can be located on different envelope proteins. (B) The difference between the two models is the highest, if the fraction of one mutant is fixed at 0.265. (C) The relative infectivity for an experimental system in which the fraction of one mutant is fixed at maximum distinguishability and the fraction of the other mutant envelope protein is varied.

Inline graphic — . (A) The relative infectivity is shown as a function of the fractions of envelope proteins defective of function A, , and the fraction of envelope proteins defective of function B, . The grey plane shows the predictions for a model in which the two functional units A and B are located on the same envelope protein, the blue plane the model in which these function can be located on different envelope proteins. (B) The difference between the two models is the highest, if the fraction of one mutant is fixed at 0.265. (C) The relative infectivity for an experimental system in which the fraction of one mutant is fixed at maximum distinguishability and the fraction of the other mutant envelope protein is varied.