Evidence map›Paper›PMID 23886911›Full record

ReviewMethods (San Diego, Calif.)2014

pCAP-based peptide substrates: the new tool in the box of tyrosine phosphatase assays.

Stephanie M Stanford, Divya Krishnamurthy, Rhushikesh A Kulkarni, Caitlin E Karver, Eveline Bruenger, Logan M Walker, Chen-Ting Ma, Thomas D Y Chung, Eduard Sergienko, Nunzio Bottini and 1 more

Abstract readReview
In one paragraph

Review in Methods (San Diego, Calif.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.4field-weighted citation impact, top 34% of its field
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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Fluorogenic probes for imaging cellular phosphatase activity.Current opinion in chemical biology · 2020
    Review
  3. Interrogating Protein Phosphatases with Chemical Activity Probes.Chemistry (Weinheim an der Bergstrasse, Germany) · 2018
    Review
  4. Article
  5. Review
  6. 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

11 authors at 4 institutions in 1 country.

Stephanie M StanfordDivision of Cellular Biology, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037, USA.
Divya KrishnamurthyDepartment of Chemistry, University of Southern California, Los Angeles, CA 90089, USA; Department of Medicinal Chemistry, University of Utah, Salt Lake City, UT 84112, USA.
Rhushikesh A KulkarniDepartment of Medicinal Chemistry, University of Utah, Salt Lake City, UT 84112, USA.
Caitlin E KarverDepartment of Chemistry, University of Southern California, Los Angeles, CA 90089, USA; Department of Medicinal Chemistry, University of Utah, Salt Lake City, UT 84112, USA.
Eveline BruengerDepartment of Medicinal Chemistry, University of Utah, Salt Lake City, UT 84112, USA.
Logan M WalkerDivision of Cellular Biology, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037, USA.
Chen-Ting MaConrad Prebys Center for Chemical Genomics, Sanford|Burnham Medical Research Institute, La Jolla, CA 92037, USA.
Thomas D Y ChungConrad Prebys Center for Chemical Genomics, Sanford|Burnham Medical Research Institute, La Jolla, CA 92037, USA.
Eduard SergienkoConrad Prebys Center for Chemical Genomics, Sanford|Burnham Medical Research Institute, La Jolla, CA 92037, USA.
Nunzio BottiniDivision of Cellular Biology, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037, USA. Electronic address: nunzio@liai.org.
Amy M BarriosDepartment of Medicinal Chemistry, University of Utah, Salt Lake City, UT 84112, USA. Electronic address: amy.barrios@utah.edu.
University of Utah · USLa Jolla Institute for Immunology · USSanford Burnham Prebys Medical Discovery Institute · USUniversity of Southern California · US

Funding

Sanford-Burnham Center for Chemical GenomicsU54HG005033 · NHGRI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI JACKSON, MICHAEL · 2008 to 2012
$72.5M
Fluorogenic Assays for Cell-based HTS of Tyrosine Phosphatase InhibitorsR01DK080165 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI BOTTINI, NUNZIO · 2008 to 2012
$1.5M
Imaging Protein Tyrosine Phosphorylation in vivoR21GM079386 · NIGMS · UNIVERSITY OF UTAH · PI BARRIOS, AMY M · 2007 to 2008
$443k
Fluorogenic PTP Assay for Use in HTS of Novel LYP InhibitorsR21NS056945 · NINDS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI BOTTINI, NUNZIO · 2006 to 2008
$244k
NHGRI NIH HHS U54 HG005033NHGRI NIH HHS U54HG005033NIDDK NIH HHS R01 DK080165NIGMS NIH HHS R21 GM079386NINDS NIH HHS R21 NS056945NINDS NIH HHS R21 NS056945-01
6 · The paper itself

Abstract

Robust, facile high throughput assays based on non-peptidic probes are available to detect the enzyme activity of protein tyrosine phosphatases. However, these assays cannot replace the use of peptide-based probes in many applications; for example when a closer mimic of the physiological target is desired or in substrate profiling expeditions. Phosphotyrosine peptides are often used in these assays, but their use is complicated by either poor sensitivity or the need for indirect detection methods, among other pitfalls. Novel peptide-based probes for protein tyrosine phosphatases are needed to replace phosphotyrosine peptides and accelerate the field of tyrosine phosphatase substrate profiling. Here we review a type of peptidic probe for tyrosine phosphatases, which is based on the incorporation of the phosphotyrosine-mimic phosphocoumaryl amino propionic acid (pCAP) into peptides. The resulting fluorogenic pCAP peptides are dephosphorylated by tyrosine phosphatases with similar efficiency as the homologous phosphotyrosine peptides. pCAP peptides outperform phosphotyrosine peptides, providing an assay that is as robust, sensitive and facile as the non-peptidic fluorogenic probes on the market. Finally the use of pCAP can expand the range of phosphatase assays, facilitating the investigation of multiphosphorylated peptides and providing an in-gel assay for phosphatase activity.

Indexed as

AlanineBiological AssayCoumarinsElectrophoresis, Polyacrylamide GelFluorescent DyesHumansOrganophosphatesPeptidesProtein Tyrosine PhosphatasesSubstrate SpecificityAlanineCoumarinsFluorescent DyesOrganophosphatesPeptidesProtein Tyrosine PhosphatasesEnzyme activity gelFluorogenic enzyme substratesHigh-throughput screeningMultiply phosphorylated peptidesPeptide synthesis

Identifiers

PMID23886911
PMCPMC3899110
OpenAlexW2067661561

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.