Evidence map›Paper›PMID 23285056›Full record

ArticlePloS one2012

Enhancing endosomal escape of transduced proteins by photochemical internalisation.

Kevin Mellert, Markus Lamla, Klaus Scheffzek, Rainer Wittig, Dieter Kaufmann

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

20 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
  2. Article
  3. Targeting the Inside of Cells with Biologicals: Chemicals as a Delivery Strategy.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2021
    Review
  4. Article
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  7. Irreversible Protein Labeling by Paal-Knorr Conjugation.Chembiochem : a European journal of chemical biology · 2017
    Article
  8. Intracellular delivery of proteins by nanocarriers.Nanomedicine (London, England) · 2017
    Review
  9. Article
  10. Nanotechnology for protein delivery: Overview and perspectives.Journal of controlled release : official journal of the Controlled Release Society · 2016
    Review
  11. Article
  12. Article
  13. Near-infrared light activated delivery platform for cancer therapy.Advances in colloid and interface science · 2015
    Review
  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 at 4 institutions in 2 countries.

Kevin MellertInstitute of Human Genetics, University of Ulm, Ulm, Germany. kevin.mellert@uni-ulm.de
Markus Lamla
Klaus Scheffzek
Rainer Wittig
Dieter Kaufmann
Universität Ulm · DEInnsbruck Medical University · ATInstitute for Laser Technology in Medicine and Measurement Technique · DETechnische Hochschule Ulm · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Induced internalisation of functional proteins into cultured cells has become an important aspect in a rising number of in vitro and in vivo assays. The endo-lysosomal entrapment of the transduced proteins remains the major problem in all transduction protocols. In this study we compared the efficiency, cytotoxicity and protein targeting of different commercially available transduction reagents by transducing a well-studied fluorescently labelled protein (Atto488-bovine serum albumin) into cultured human sarcoma cells. The amount of internalised protein and toxicity differed between the different reagents, but the percentage of transduced cells was consistently high. Furthermore, in all protocols the signals of the transduced Atto488-BSA were predominantly punctual consistent with an endosomal localisation. To overcome the endosomal entrapment, the transduction protocols were combined with a photochemical internalisation (PCI) treatment. Using this combination revealed that an endosomal disruption is highly effective in cell penetrating peptide (CPP) mediated transduction, whereas lipid-mediated transductions lead to a lower signal spreading throughout the cytosol. No change in the signal distribution could be achieved in treatments using non-lipid polymers as a transduction reagent. Therefore, the combination of protein transduction protocols based on CPPs with the endosomolytic treatment PCI can facilitate protein transduction experiments in vitro.

Indexed as

EndocytosisPhotochemical ProcessesTransduction, GeneticAnimalsCattleCell DeathCell Line, TumorChild, PreschoolEndosomesFluorescenceFluorescent DyesHumansIndicators and ReagentsLuminescent ProteinsSerum Albumin, BovineSignal Processing, Computer-AssistedFluorescent DyesIndicators and ReagentsLuminescent ProteinsSerum Albumin, Bovine

Identifiers

PMID23285056
PMCPMC3528648
OpenAlexW2042209314

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.