Addition/Correction pubs.acs.org/jpr
Correction to “Label-Free Quantitative Proteomics Reveals the Dynamics of Proteasome Complexes Composition and Stoichiometry in a Wide Range of Human Cell Lines” Bertrand Fabre, Thomas Lambour, Luc Garrigues, Manuelle Ducoux-Petit, François Amalric, Bernard Monsarrat, Odile Burlet-Schiltz, and Marie-Pierre Bousquet-Dubouch* J. Proteome Res. 2014, 13 (6), 3027−3037. DOI: 10.1021/pr500193k S Supporting Information *
The goal of this study was indeed to unravel the different levels of structural composition of human proteasomes (20S core subtypes, main activators, main associated proteins, and assembly chaperones), thus giving access to important information about the dynamics of functional regulation of proteasome activity. As this paper focuses more on determining the overall proteasome complex composition and stoichiometry using a large panel of cell lines rather than studying the proteasome composition in
Due to an error during manuscript preparation, the names of the cell lines used in the original paper were erroneously attributed to MS data. As a consequence, the labeling of four graphs from Figure 2B, Figure 4B,C, and Figure 5C has been corrected in Figure 1 below. The corrected Supporting Information (corrected column titles in Excel file) is also provided. Importantly, the main results and conclusions are not affected by these changes.
Figure 1. Corrected Figure 2B, Figure 4B,C, and Figure 5C. Published: September 25, 2014 © 2014 American Chemical Society
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Addition/Correction
each particular cell line, mislabeling of some graphs does not affect the main conclusions of this research article. We sincerely apologize for this regrettable mistake and for any confusion this may have caused.
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ASSOCIATED CONTENT
S Supporting Information *
Corrected Supplementary Table (corrected column titles in Excel file). This material is available free of charge via the Internet at http://pubs.acs.org.
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