Evidence map›Paper›PMID 24088168›Full record

ArticleAnalytical chemistry2013

Profiling deacetylase activities in cell lysates with peptide arrays and SAMDI mass spectrometry.

Hsin-Yu Kuo, Teresa A DeLuca, William M Miller, Milan Mrksich

Abstract read
In one paragraph

Article in Analytical chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
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  11. Review
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  15. Cellular Assays with a Molecular Endpoint Measured by SAMDI Mass Spectrometry.Small (Weinheim an der Bergstrasse, Germany) · 2016
    Article
  16. Article
  17. 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

4 authors.

Hsin-Yu Kuo *Departments of Biomedical Engineering, Chemistry, Cell & Molecular Biology, Northwestern University, Evanston, Illinois 60208.
Teresa A DeLuca *Department of Chemical and Biological Engineering, Northwestern University, Evanston, Illinois 60208.
William M MillerDepartment of Chemical and Biological Engineering, Northwestern University, Evanston, Illinois 60208.
Milan MrksichDepartments of Biomedical Engineering, Chemistry, Cell & Molecular Biology, Northwestern University, Evanston, Illinois 60208.

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Daniela E Matei · 1993 to 2026
$153.9M
TRANS-NETWORK PROJECTSU54CA143869 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI MARKO, JOHN F · 2009 to 2013
$12.8M
CARCINOGENESIS TRAINING PROGRAMT32CA009560 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Kathleen Janee Green · 1986 to 2026
$8.4M
Peptide Arrays for Understanding Histone BiochemistryR01GM084188 · NIGMS · UNIVERSITY OF CHICAGO · PI MRKSICH, MILAN · 2008 to 2011
$1.2M
Bioengineering challenges for platelet production from hematopoietic stem cellsR01HL093083 · NHLBI · NORTHWESTERN UNIVERSITY · PI MILLER, WILLIAM M · 2009 to 2010
$688k
NCI NIH HHS CA060553NCI NIH HHS P30 CA060553NCI NIH HHS T32 CA009560NCI NIH HHS T32 CA09560NCI NIH HHS U54 CA143869NCI NIH HHS U54CA143869NHLBI NIH HHS HL93083NHLBI NIH HHS R01 HL093083NIGMS NIH HHS GM084188NIGMS NIH HHS R01 GM084188
6 · The paper itself

Abstract

The development of arrays that can profile molecular activities in cells is important to understanding signaling pathways in normal and pathological settings. While oligonucleotide arrays are now routinely used to profile global gene expression, there is still a lack of tools for profiling enzyme activities in cell lysates. This paper describes the combination of peptide arrays formed on self-assembled monolayers and mass spectrometry to provide a label-free approach for identifying patterns of enzyme activities in cell lysates. The approach is demonstrated by profiling lysine deacetylase (KDAC) activities in cell lysates of the CHRF megakaryocytic (Mk) cell line. Class-specific deacetylase inhibitors were used to show that terminal Mk differentiation of CHRF cells is marked by a pronounced decrease in sirtuin activity and by little change in activity of KDACs 1-11. This work establishes a platform that can be used to identify changes in global activity profiles of cell lysates for a wide variety of enzymatic activities.

Indexed as

Protein Array AnalysisAcetylationBlotting, WesternCells, CulturedFlow CytometryHistone DeacetylasesHumansMass SpectrometryMegakaryocytesPeptide FragmentsPeptide LibrarySignal TransductionSubstrate SpecificityHistone DeacetylasesPeptide FragmentsPeptide Library

Identifiers

PMID24088168
PMCPMC3912874

What OpenQuestion holds

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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.