Helmholtz Gemeinschaft

Search
Browse
Statistics
Feeds

UbiFast, a rapid and deep-scale ubiquitylation profiling approach for biology and translational research

[img]
Preview
PDF - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader
6MB
Item Type:Preprint
Title:UbiFast, a rapid and deep-scale ubiquitylation profiling approach for biology and translational research
Creators Name:Udeshi, N.D. and Mani, D.C. and Satpathy, S. and Fereshetian, S. and Gasser, J.A. and Svinkina, T. and Ebert, B.L. and Mertins, P. and Carr, S.A.
Abstract:Protein ubiquitylation is involved in a plethora of cellular processes. Defects in the ubiquitin system are at the root of many acquired and hereditary diseases. While antibodies directed at ubiquitin remnants (K-ε-GG) have improved the ability to monitor ubiquitylation using mass spectrometry, methods for highly-multiplexed measurement of ubiquitylation in tissues and primary cells using sub-milligram amounts of sample remains a challenge. Here we present a highly-sensitive, rapid and multiplexed protocol for quantifying ∼10,000 ubiquitylation sites from as little as 500 ug peptide per sample from cells or tissue in a TMT10 plex in ca. 5 hr. High-field Asymmetric Ion Mobility Spectrometry (FAIMS) is used to improve quantitative accuracy for posttranslational modification analysis. We use the approach to rediscover substrates of the E3 ligase targeting drug lenalidomide and to identify proteins modulated by ubiquitylation in models of basal and luminal human breast cancer. The sensitivity and speed of the UbiFast method makes it suitable for large-scale studies in primary tissue samples.
Source:bioRxiv
Publisher:Cold Spring Harbor Laboratory Press
Article Number:785378
Date:27 September 2019
Official Publication:https://doi.org/10.1101/785378

Repository Staff Only: item control page

Downloads

Downloads per month over past year

Open Access
MDC Library