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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Disclosures
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

We present a method for the purification, detection, and identification of diGly peptides that originate from ubiquitinated proteins from complex biological samples. The presented method is reproducible, robust, and outperforms published methods with respect to the level of depth of the ubiquitinome analysis.

Abstract

The posttranslational modification of proteins by the small protein ubiquitin is involved in many cellular events. After tryptic digestion of ubiquitinated proteins, peptides with a diglycine remnant conjugated to the epsilon amino group of lysine ('K-ε-diglycine' or simply 'diGly') can be used to track back the original modification site. Efficient immunopurification of diGly peptides combined with sensitive detection by mass spectrometry has resulted in a huge increase in the number of ubiquitination sites identified up to date. We have made several improvements to this workflow, including offline high pH reverse-phase fractionation of peptides prior to the enrichment procedure, and the inclusion of more advanced peptide fragmentation settings in the ion routing multipole. Also, more efficient cleanup of the sample using a filter-based plug in order to retain the antibody beads results in a greater specificity for diGly peptides. These improvements result in the routine detection of more than 23,000 diGly peptides from human cervical cancer cells (HeLa) cell lysates upon proteasome inhibition in the cell. We show the efficacy of this strategy for in-depth analysis of the ubiquitinome profiles of several different cell types and of in vivo samples, such as brain tissue. This study presents an original addition to the toolbox for protein ubiquitination analysis to uncover the deep cellular ubiquitinome.

Introduction

The conjugation of ubiquitin to proteins marks them for degradation by the proteasome and is a crucial process in proteostasis. The C-terminal carboxyl group of ubiquitin forms an isopeptide bond with the lysine ε-amino group of the target protein1,2. In addition, ubiquitin can be attached to other ubiquitin modules, resulting in the formation of homogeneous (i.e., K48 or K11) or branched (i.e., heterogeneous or mixed) polyubiquitin structures1,3. The most well-known function of ubiquitin is its role in proteasomal degradation, mediated by K48-lin....

Protocol

All methods described here have been approved by the Institutional Animal Care and Use Committee (EDC) of Erasmus MC.

1. Sample preparation

  1. Cultured cells
    1. Select a cell line of interest (e.g., HeLa or osteosarcoma [U2OS] cells) and grow the cells in Dulbecco's Minimal Eagle Medium (DMEM) supplemented with 10% heat inactivated fetal bovine serum (FBS) and 100 units/mL penicillin/streptomycin.
    2. For quantitative proteomics experiments, culture cells in DMEM lacking arginine and lysine. The medium must be supplemented with 10% dialyzed fetal bovine serum (FBS), 100 units/mL penicillin/streptomycin, and alan....

Representative Results

Ubiquitinated proteins leave a 114.04 Da diglycine remnant on the target lysine residue when the proteins are digested with trypsin. The mass difference caused by this motif was used to unambiguously recognize the site of ubiquitination in a mass spectrometry experiment. The strategy that we describe here is a state-of-the-art method for the enrichment and subsequent identification of diGly peptides by nanoflow LC-MS/MS (Figure 1A). In this s.......

Discussion

The protocol described here was applied to samples from various biological sources, such as cultured cells and in vivo tissue. In all cases we identified thousands of diGly peptides, provided that the total protein input amount was at least 1 mg. The enrichment using specific antibodies is highly efficient, given that only at most 100-150 very low abundant diGly peptides were identified from whole cell lysates if no enrichment procedures for ubiquitinated proteins or diGly peptides were applied. Obviously, sensitive mass.......

Disclosures

The authors declare no conflict of interest.

Acknowledgements

This work is part of the project "Proteins at Work", a program of the Netherlands Proteomics Centre financed by The Netherlands Organization for Scientific Research (NWO) as part of the National Roadmap Large-Scale Research Facilities (project number 184.032.201).

....

Materials

NameCompanyCatalog NumberComments
1,4-DithioerythritolSigma-AldrichD8255
3M Empore C18 Octadecyl disksSupelco66883-Uproduct discontinued at Supelco; CDS Analytical is the new manufacturer (https://www.cdsanalytical.com/empore)
Ammonium formateSigma-Aldrich70221
BortezomibUBPbio
CSH130 resin, 3.5 μm, 130 ÅWaters
Dimethylsulfoxide (DMSO)Sigma-Aldrich34869
DMEMThermoFisher
EASY-nanoLC 1200ThermoFisher
FBSGibco
GF/F filter plugWhatman1825-021
IodoacetamideSigma-AldrichI6125
Lysine, ArginineSigma-Aldrich
Lysine-8 (13C6;15N2), Arginine-10 (13C6;15N4)Cambridge Isotope Laboratories
Lysyl Endopeptidase(LysC)Wako Pure Chemicals129-02541
NanoLC ovenMPI design, MS Wil GmbH
N-Lauroylsarcosine sodium saltSigma-AldrichL-5125
Orbitrap Fusion Lumos mass spectrometerThermoFisher
Pierce BCA Protein Assay KitThermoFisher / Pierce23225
PLRP-S (300 Å, 50 µm) polymeric reversed phase particlesAgilent TechnologiesPL1412-2K01
PTMScan Ubiquitin Remnant Motif (K-ε-GG) KitCell Signaling Technologies5562
Sep-Pak tC18 6 cc Vac CartridgeWatersWAT036790Remove the tC18 material from the cartridge before filling the cartridge with PLRP-S
Sodium deoxycholateSigma-Aldrich30970
Tris-baseSigma-AldrichT6066
Tris-HClSigma-AldrichT5941
Trypsin, TPCK TreatedThermoFisher20233

References

  1. Clague, M. J., Urbé, S. Ubiquitin: Same molecule, different degradation pathways. Cell. 143, 682-685 (2010).
  2. Ciechanover, A. The ubiquitin-proteasome proteolytic pathway. Cell. 79 (1), 13-21 (1995).<....

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