Evidence map›Paper›PMID 36586285›Full record

ArticleJournal of chromatography. A2023

Increase the flow rate and improve hydrogen deuterium exchange mass spectrometry.

Daniele Peterle, David DePice, Thomas E Wales, John R Engen

Abstract read
In one paragraph

Article in Journal of chromatography. A, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. MultiPassMerger: Automated data processing for multipass cyclic ion mobility HDX-MS.Protein science : a publication of the Protein Society · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Daniele PeterleDepartment of Chemistry and Chemical Biology, Northeastern University, Mailstop 412 TF, 360 Huntington Avenue, Boston, MA 02115, United States.
David DePiceDepartment of Chemistry and Chemical Biology, Northeastern University, Mailstop 412 TF, 360 Huntington Avenue, Boston, MA 02115, United States.
Thomas E WalesDepartment of Chemistry and Chemical Biology, Northeastern University, Mailstop 412 TF, 360 Huntington Avenue, Boston, MA 02115, United States.
John R EngenDepartment of Chemistry and Chemical Biology, Northeastern University, Mailstop 412 TF, 360 Huntington Avenue, Boston, MA 02115, United States. Electronic address: j.engen@northeastern.edu.

Funding

Dissecting and Targeting Deregulated Mitochondrial Apoptosis in Human CancerR35CA197583 · NCI · DANA-FARBER CANCER INST · PI Loren David Walensky · 2015 to 2026
$12.5M
STRUCTURAL STUDIES OF A T CELL SPECIFIC TYROSINE KINASER01AI043957 · NIAID · IOWA STATE UNIVERSITY · PI AMY H ANDREOTTI, LESLIE JOAN BERG · 1999 to 2026
$9.5M
Structural Thermodynamics of Human Apolipoprotein C-1R01GM067260 · NIGMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI GURSKY, OLGA · 2003 to 2024
$7.4M
Structure and Function of Serum Amyloid A in Health and DiseaseR01GM135158 · NIGMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI Olga Gursky · 2020 to 2026
$2.4M
Conformational Regulation and Therapeutic Targeting of Oncogenic KRASR01CA233978 · NCI · NORTHEASTERN UNIVERSITY · PI WALENSKY, LOREN DAVID, WALES, THOMAS EDWARD · 2020 to 2024
$2.4M
NCI NIH HHS R01 CA233978NCI NIH HHS R35 CA197583NIAID NIH HHS R01 AI043957NIGMS NIH HHS R01 GM067260NIGMS NIH HHS R01 GM135158
6 · The paper itself

Abstract

Reversed-phase peptide separation in hydrogen deuterium exchange (HDX) mass spectrometry (MS) must be done with conditions where the back exchange is the slowest possible, the so-called quench conditions of low pH and low temperature. To retain maximum deuterium, separation must also be done as quickly as possible. The low temperature (0 °C) of quench conditions complicates the separation and leads primarily to a reduction in separation quality and an increase in chromatographic backpressure. To improve the separation in HDX MS, one could use a longer gradient, smaller particles, a different separation mechanism (for example, capillary electrophoresis), or multi-dimensional separations such as combining ion mobility separation with reversed-phase separation. Another way to improve separations under HDX MS quench conditions is to use a higher flow rate where separation efficiency at 0 °C is more ideal. Higher flow rates, however, require chromatographic systems (both pumps and fittings) with higher backpressure limits. We tested what improvements could be realized with a commercial UPLC/UHPLC system capable of ∼20,000 psi backpressure. We found that a maximum flow rate of 225 µL/min (using a 1 × 50 mm column packed with 1.8 µm particles) was possible and that higher flow rate clearly led to higher peak capacity. HDX MS analysis of both simple and particularly complex samples improved, permitting both shorter separation time, if desired, and providing more deuterium recovery.

Indexed as

Deuterium Exchange MeasurementHydrogen Deuterium Exchange-Mass SpectrometryDeuteriumHydrogenMass SpectrometryPeptidesDeuteriumHydrogenPeptidesHDX MSLow temperature separationMass spectrometryPeak capacityUPLC/UHPLC

Identifiers

PMID36586285
PMCPMC9872520

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.