Evidence map›Paper›PMID 22900707›Full record

ArticleBioconjugate chemistry2012

Caspase-activated cell-penetrating peptides reveal temporal coupling between endosomal release and apoptosis in an RGC-5 cell model.

James R Johnson, Brandon Kocher, Edward M Barnett, Jayne Marasa, David Piwnica-Worms

Abstract read
In one paragraph

Article in Bioconjugate chemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

19 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Intracellular delivery of proteins by nanocarriers.Nanomedicine (London, England) · 2017
    Review
  10. Article
  11. MMP-2/9-Specific Activatable Lifetime Imaging Agent.Sensors (Basel, Switzerland) · 2015
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Image-Guided Tumor Resection.Cancer journal (Sudbury, Mass.)
    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

5 authors at 1 institution in 1 country.

James R JohnsonMolecular Imaging Center, Mallinckrodt Institute of Radiology, BRIGHT Institute, Department of Cell Biology & Physiology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Brandon Kocher
Edward M Barnett
Jayne Marasa
David Piwnica-Worms
Mallinckrodt (United States) · US

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI TIMOTHY J. EBERLEIN · 2001 to 2026
$128.0M
WU-MDACC Inter-Institutional Molecular Imaging CenterP50CA094056 · NCI · WASHINGTON UNIVERSITY · PI KOPAN, RAPHAEL · 2002 to 2016
$26.3M
MOLECULAR ONCOLOGY TRAINING GRANTT32CA113275 · NCI · WASHINGTON UNIVERSITY · PI Matthew J Walter · 2006 to 2026
$5.7M
MEMBRANE PERMEANT PEPTIDES FOR IMAGING CELL FUNCTIONR01EY019587 · NEI · WASHINGTON UNIVERSITY · PI PIWNICA-WORMS, DAVID · 2009 to 2022
$5.3M
MEMBRANE PERMEANT PEPTIDES FOR IMAGING CELL FUNCTIONR01CA082841 · NCI · WASHINGTON UNIVERSITY · PI PIWNICA-WORMS, DAVID · 1999 to 2008
$3.0M
Caspase Activated Probes For In Vivo Optical Imaging of Retinal NeurodegenerationF32EY020051 · NEI · WASHINGTON UNIVERSITY · PI JOHNSON, JAMES RUSSELL · 2010 to 2012
$161k
NCI NIH HHS P30 CA091842NCI NIH HHS P50 CA094056NCI NIH HHS P50 CA94056NCI NIH HHS R01 CA082841NCI NIH HHS T32 CA113275NEI NIH HHS F32 EY020051NEI NIH HHS F32 EY20051-01NEI NIH HHS R01 EY019587
6 · The paper itself

Abstract

Caspase-activatable cell-penetrating peptide (CPP) probes, designed for efficient cell uptake and specificity via cleavable intramolecular quenched-fluorophore strategies, show promise for identifying and imaging retinal ganglion cell apoptosis in vivo. However, initial cell uptake and trafficking events cannot be visualized because the probes are designed to be optically quenched in the intact state. To visualize subcellular activation events in real-time during apoptosis, a new series of matched quenched and nonquenched CPP probes were synthesized. In both native and staurosporine-differentiated RGC-5 cells, probe uptake was time- and concentration-dependent through clathrine-, caveolin-, and pinocytosis-mediated endocytic mechanisms. During apoptosis, KcapTR488, a novel dual fluorophore CPP probe, revealed by multispectral imaging a temporal coupling of endosomal release and effector caspase activation in RGC-5 cells. The novel CPPs described herein provide new tools to study spatial and temporal regulation of endosomal permeability during apoptosis.

Indexed as

ApoptosisCaspasesCell DifferentiationCell LineEndosomesFlow CytometryHumansImmunohistochemistryPeptidesCaspasesPeptides

Identifiers

PMID22900707
PMCPMC3447108
OpenAlexW2087567974

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.