| Literature DB >> 33900084 |
Jiaming Li1, Zhenying Cai2,3, Ryan D Bomgarden4, Ian Pike5, Karsten Kuhn5, John C Rogers4, Thomas M Roberts2,3, Steven P Gygi1, Joao A Paulo1.
Abstract
The development of the TMTpro-16plex series expanded the breadth of commercial isobaric tagging reagents by nearly 50% over classic TMT-11plex. In addition to the described 16plex reagents, the proline-based TMTpro molecule can accommodate two additional combinations of heavy carbon and nitrogen isotopes. Here, we introduce the final two labeling reagents, TMTpro-134C and TMTpro-135N, which permit the simultaneous global protein profiling of 18 samples with essentially no missing values. For example, six conditions with three biological replicates can now be perfectly accommodated. We showcase the 18plex reagent set by profiling the proteome and phosphoproteome of a pair of isogenic mammary epithelial cell lines under three conditions in triplicate. We compare the depth and quantitative performance of this data set with a TMTpro-16plex experiment in which two samples were omitted. Our analysis revealed similar numbers of quantified peptides and proteins, with high quantitative correlation. We interrogated further the TMTpro-18plex data set by highlighting changes in protein abundance profiles under different conditions in the isogenic cell lines. We conclude that TMTpro-18plex further expands the sample multiplexing landscape, allowing for complex and innovative experimental designs.Entities:
Keywords: 18plex; BYL-719; KIN-193; MCF10A; PTEN; TMTpro; eclipse; real-time search
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Year: 2021 PMID: 33900084 PMCID: PMC8210943 DOI: 10.1021/acs.jproteome.1c00168
Source DB: PubMed Journal: J Proteome Res ISSN: 1535-3893 Impact factor: 4.466