Evidence map›Paper›PMID 29185444›Full record

ArticleNature communications2017

Directing intracellular supramolecular assembly with N-heteroaromatic quaterthiophene analogues.

David Y W Ng, Roman Vill, Yuzhou Wu, Kaloian Koynov, Yu Tokura, Weina Liu, Susanne Sihler, Andreas Kreyes, Sandra Ritz, Holger Barth and 2 more

Abstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Polymer Chemistry in Living Cells.Accounts of chemical research · 2022
    Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. 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

12 authors.

David Y W NgMax Planck Institute for Polymer Research, Ackermannweg 10, 55128, Mainz, Germany. david.ng@mpip-mainz.mpg.de.ORCID http://orcid.org/0000-0002-0302-0678
Roman VillInstitute of Organic Chemistry III, Ulm University, Albert-Einstein-Allee 11, 89081, Ulm, Germany.ORCID http://orcid.org/0000-0001-6335-5050
Yuzhou WuMax Planck Institute for Polymer Research, Ackermannweg 10, 55128, Mainz, Germany.
Kaloian KoynovMax Planck Institute for Polymer Research, Ackermannweg 10, 55128, Mainz, Germany.
Yu TokuraMax Planck Institute for Polymer Research, Ackermannweg 10, 55128, Mainz, Germany.
Weina LiuMax Planck Institute for Polymer Research, Ackermannweg 10, 55128, Mainz, Germany.
Susanne SihlerInstitute of Organic Chemistry III, Ulm University, Albert-Einstein-Allee 11, 89081, Ulm, Germany.
Andreas KreyesInstitute of Organic Chemistry III, Ulm University, Albert-Einstein-Allee 11, 89081, Ulm, Germany.
Sandra RitzInstitute of Molecular Biology, Ackermannweg 4, 55128, Mainz, Germany.
Holger BarthInstitute of Pharmacology and Toxicology, Ulm University Medical Center, Albert-Einstein-Allee 11, 89081, Ulm, Germany.
Ulrich ZienerInstitute of Organic Chemistry III, Ulm University, Albert-Einstein-Allee 11, 89081, Ulm, Germany. ulrich.ziener@uni-ulm.de.
Tanja WeilMax Planck Institute for Polymer Research, Ackermannweg 10, 55128, Mainz, Germany. weil@mpip-mainz.mpg.de.ORCID http://orcid.org/0000-0002-5906-7205

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Self-assembly in situ, where synthetic molecules are programmed to organize in a specific and complex environment i.e., within living cells, can be a unique strategy to influence cellular functions. Here we present a small series of rationally designed oligothiophene analogues that specifically target, locate and dynamically self-report their supramolecular behavior within the confinement of a cell. Through the recognition of the terminal alkyl substituent and the amphiphilic pyridine motif, we show that the cell provides different complementary pathways for self-assembly that can be traced easily with fluorescence microscopy as their molecular organization emits in distinct fluorescent bands. Importantly, the control and induction of both forms are achieved by time, temperature and the use of the intracellular transport inhibitor, bafilomycin A1. We showcase the importance of both intrinsic (cell) and extrinsic (stimulus) factors for self-organization and the potential of such a platform toward developing synthetic functional components within living cells.

Indexed as

A549 CellsBiological TransportCell SurvivalChemistry Techniques, SyntheticHeLa CellsHumansMacrolidesMicroscopy, ConfocalMicroscopy, FluorescenceMolecular BiologyMolecular ImagingSerum Albumin, HumanSolutionsSpectrometry, FluorescenceStructure-Activity RelationshipTemperaturebafilomycin A1MacrolidesSerum Albumin, HumanSolutionsThiophenes

Identifiers

PMID29185444
PMCPMC5707410

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.