Evidence map›Paper›PMID 27702615›Full record

ArticleJournal of chromatography. A2016

Development of a 45kpsi ultrahigh pressure liquid chromatography instrument for gradient separations of peptides using long microcapillary columns and sub-2μm particles.

Kaitlin M Grinias, Justin M Godinho, Edward G Franklin, Jordan T Stobaugh, James W Jorgenson

Abstract read
In one paragraph

Article in Journal of chromatography. A, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. [Recent advances in microchip liquid chromatography].Se pu = Chinese journal of chromatography · 2021
    Article
  10. Review
  11. Article
  12. Article
  13. Liquid chromatography above 20,000 PSI.Trends in analytical chemistry : TRAC · 2020
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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

5 authors.

Kaitlin M GriniasDepartment of Chemistry, The University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599-3290, United States.
Justin M GodinhoDepartment of Chemistry, The University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599-3290, United States.
Edward G FranklinDepartment of Chemistry, The University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599-3290, United States.
Jordan T StobaughDepartment of Chemistry, The University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599-3290, United States.
James W JorgensonDepartment of Chemistry, The University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599-3290, United States. Electronic address: jj@unc.edu.

Funding

Statistics and Bioinformatics Core - WangU24DK097153 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BURANT, CHARLES F · 2012 to 2017
$10.1M
High Resolution MetabolomicsR01DK101473 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KENNEDY, ROBERT T · 2015 to 2018
$1000k
NIDDK NIH HHS R01 DK101473NIDDK NIH HHS U24 DK097153
6 · The paper itself

Abstract

Commercial chromatographic instrumentation for bottom-up proteomics is often inadequate to resolve the number of peptides in many samples. This has inspired a number of complex approaches to increase peak capacity, including various multidimensional approaches, and reliance on advancements in mass spectrometry. One-dimensional reversed phase separations are limited by the pressure capabilities of commercial instruments and prevent the realization of greater separation power in terms of speed and resolution inherent to smaller sorbents and ultrahigh pressure liquid chromatography. Many applications with complex samples could benefit from the increased separation performance of long capillary columns packed with sub-2μm sorbents. Here, we introduce a system that operates at a constant pressure and is capable of separations at pressures up to 45kpsi. The system consists of a commercially available capillary liquid chromatography instrument, for sample management and gradient creation, and is modified with a storage loop and isolated pneumatic amplifier pump for elevated separation pressure. The system's performance is assessed with a complex peptide mixture and a range of microcapillary columns packed with sub-2μm C18 particles.

Indexed as

Chromatography, High Pressure LiquidParticle SizePeptidesPressurePeptidesCapillary chromatographyLC–MSPeptidesProteomicsUHPLC

Identifiers

PMID27702615
PMCPMC5084847

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.