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. 2015 Mar 23;10(3):e0122177. doi: 10.1371/journal.pone.0122177

Correction: Increased N-Glycosylation Efficiency by Generation of an Aromatic Sequon on N135 of Antithrombin

The PLOS ONE Staff
PMCID: PMC4370769  PMID: 25799579

The images for Figs. 3 and 4 are incorrectly switched. The image that appears as Fig. 3 should be Fig. 4, and the image that appears as Fig. 4 should be Fig. 3. The figure legends appear in the correct order.

Fig 3. Function of antithrombin variants.

Fig 3

Anti-FXa activity of antithrombin proteins secreted to the conditioned medium in presence of heparin. Results are expressed as a percentage of the activity of the S137T variant. Each bar represents the mean ± standard deviation (SD) of two independent experiments performed in duplicate. The differences between mutants were tested by paired t-test (p-value). The “*” indicated differences statistically significant with p<0.05.

Fig 4. Scheme of binding of antithrombin and heparin.

Fig 4

Initial rapid equilibrium, K 1, between antithrombin, AT, and pentasaccharide, H, leads to complex, AT.H, followed by rapid conformational change via k 2 to a high heparin affinity, highly fluorescence complex, AT*.H.

There are errors in the Van't Hoff equation under the Materials and Methods subsection titled “Determination of denaturing temperature.” Please view the complete, correct equation here:

dG=-RTLn(Fobs-Fn0)/(Fd0-Fobs)=dHm(1-T/Tm)

Reference


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