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[2] Methods for quantification of in vivo changes in protein ubiquitination following proteasome and deubiquitinase inhibition.
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[3] Proteomic investigations reveal a role for RNA processing factor THRAP3 in the DNA damage response.
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[4] Proteomic investigations of lysine acetylation identify diverse substrates of mitochondrial deacetylase sirt3.
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[5] Integrated proteomic analysis of post-translational modifications by serial enrichment.
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[6] Refined preparation and use of anti-diglycine remnant (K-ε-GG) antibody enables routine quantification of 10,000s of ubiquitination sites in single proteomics experiments.
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