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. 2019 Mar 26;9:5218. doi: 10.1038/s41598-019-41501-w

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© The Author(s) 2019

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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MS-coupled acyl-labeling of bovine microsome RPE65. (A) Screenshots of LC-HDMS^E runs for hydroxylamine-untreated (control) and treated samples from bovine RPE microsomes. (B) MS identified peptides of bovine RPE65 (in red) corresponds to >80% sequence coverage. Numbers in superscript indicate the residue positions of the different cysteines. (C) LC-HDMS^E comparison of relative abundance of total RPE65 peptides in the control and HAM-treated bovine microsomes shows that the levels of peptides were similar. The error bars show ± standard error as calculated from the three technical replicate samples.