Evidence map›Paper›PMID 23363440›Full record

ArticleJournal of the American Chemical Society2013

Substrate-initiated synthesis of cell-penetrating poly(disulfide)s.

Eun-Kyoung Bang, Giulio Gasparini, Guillaume Molinard, Aurélien Roux, Naomi Sakai, Stefan Matile

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

39 citing papers in PubMed, 229 citations in OpenAlex.

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  15. Photo-crosslinking polymers by dynamic covalent disulfide bonds.Chemical communications (Cambridge, England) · 2021
    Article
  16. Thiol-Mediated Uptake.JACS Au · 2021
    Review
  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

6 authors at 1 institution in 1 country.

Eun-Kyoung Bang *School of Chemistry and Biochemistry, University of Geneva, Geneva, Switzerland.
Giulio Gasparini *School of Chemistry and Biochemistry, University of Geneva, Geneva, Switzerland.
Guillaume MolinardSchool of Chemistry and Biochemistry, University of Geneva, Geneva, Switzerland.
Aurélien RouxSchool of Chemistry and Biochemistry, University of Geneva, Geneva, Switzerland.
Naomi SakaiSchool of Chemistry and Biochemistry, University of Geneva, Geneva, Switzerland.
Stefan MatileSchool of Chemistry and Biochemistry, University of Geneva, Geneva, Switzerland.
University of Geneva · CH

Funding

European Research Council 311536
6 · The paper itself

Abstract

Lessons from surface-initiated polymerization are applied to grow cell-penetrating poly(disulfide)s directly on substrates of free choice. Reductive depolymerization after cellular uptake should then release the native substrates and minimize toxicity. In the presence of thiolated substrates, propagators containing a strained disulfide from asparagusic or, preferably, lipoic acid and a guanidinium cation polymerize into poly(disulfide)s in less than 5 min at room temperature at pH 7. Substrate-initiated polymerization of cationic poly(disulfide)s and their depolymerization with dithiothreitol causes the appearance and disappearance of transport activity in fluorogenic vesicles. The same process is further characterized by gel-permeation chromatography and fluorescence resonance energy transfer.

Indexed as

DisulfidesFluorescence Resonance Energy TransferHydrogen-Ion ConcentrationMolecular StructurePolymerizationPolymersTemperatureDisulfidesPolymers

Identifiers

PMID23363440
PMCPMC4601153
OpenAlexW2012596484

What OpenQuestion holds

Textmetadata
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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.