Jan 21, 2022
diDO-IPTL protocol
Forked from diDO-IPTL protocol
- Jacob Waldbauer1,
- Lichun Zhang1
- 1University of Chicago
Protocol Citation: Jacob Waldbauer, Lichun Zhang 2022. diDO-IPTL protocol. protocols.io https://dx.doi.org/10.17504/protocols.io.b36bqran
License: This is an open access protocol distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Protocol status: Working
We use this protocol and it’s working
Created: January 21, 2022
Last Modified: January 21, 2022
Protocol Integer ID: 57251
Keywords: iptl protocol isobaric peptide termini labeling, complementary derivatization of peptide termini, iptl, peptide termini, isobaric peptide, whole tandem mass spectrometry, peptide, complementary derivatization, different isotope, quantification method
Abstract
Isobaric peptide termini labeling (IPTL) is a quantification method which permits relative quantification using quantification points distributed throughout the whole tandem mass spectrometry (MS/MS) spectrum. It is based on the complementary derivatization of peptide termini with different isotopes resulting in isobaric peptides.
Troubleshooting
DAY 1
Prepare dried MS-grade trypsin, 2ug per sample to be labeled. Note that separate aliquots of dried trypsin must be used for 16O- and 18O-labeling.
Prepare two separate N-methylmorpholine (NMM) and acetic acid O-isotope exchange buffers with 16O and 18O (>98%) enriched water. Volume ratio of buffer components is 48.5 H2O : 1 NMM : 0.5 acetic acid (pH 7.4). The total volume of buffer to prepare depends on how many peptide samples are to be labeled. The protocol below is for 40µL of O-isotope exchange buffer per sample (~10-20 µg of peptide). For samples with small amounts of peptide, the concentration can be raised by adding only 20µL buffer per sample and halving the volumes of all subsequent reagent additions.
Redissolve dried trypsin aliquots in their respective O-isotope exchange buffers and transfer 40µl to each tube of dried peptide sample. KEEP TRACK of which tubes received which buffer.
Parafilm the tops of the tubes and incubate at 37ºC overnight.
DAY 2
After overnight incubation, add 2µl of 11.3M monochloroacetic acid (prepared in LC-MS grade water) to each peptide tube to lower pH down to 2.6.
Prepare 16% CH2O and CD2O formaldehyde solutions, at least 2µl per sample, diluting stocks with LC-MS grade water if necessary.
Prepare 4.8M NaBH3CN in LC-MS water. Tare 1.5mL tube, add a small amount of NaBH3CN powder in fume hood, weigh, dissolve.
Add 2µL of CH2O to each 18O tube and 2µL of CD2O to each 16O tube.
Add 2µL 4.8M NaBH3CN to each tube.
Mix well and incubate at 45ºC for 1 hr. While waiting, prepare 5M ammonium formate in LC-MS water.
Add 2µL 5M ammonium formate to each tube and mix well.
Add 8µL of formic acid to each tube and mix well. Total sample volume is ~56µl. 16O- and 18O-labeled samples are ready to be mixed and analyzed by LC-MS.