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. 2011 Jul 21;6(7):e22463. doi: 10.1371/journal.pone.0022463

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Mani 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) Protein extracts from wild type AnTat1.1 were separated on sucrose gradients. Absorption at 254 nm was recorded during fractionation of the gradient. Fractions were separated by SDS-PAGE and analyzed by immunoblotting. The ribosomal protein P0 served as a ribosome marker and the endoplasmic reticulum protein BiP as a marker for proteins not associated with ribosomes. (B) Fractionation of extracts after treatment with 50 mM EDTA, which disrupts polysomes.