Evidence map›Paper›PMID 25915163›Full record

ArticleJournal of the American Chemical Society2015

Conformational Switching of a Foldamer in a Multicomponent System by pH-Filtered Selection between Competing Noncovalent Interactions.

Julien Brioche, Sarah J Pike, Sofja Tshepelevitsh, Ivo Leito, Gareth A Morris, Simon J Webb, Jonathan Clayden

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Hydrogen Bonding within DynamicJournal of the American Chemical Society · 2026
    Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Anion-Dependent Hydrogen-Bond Polarity Switching in Ethylene-bridged Urea Oligomers.Chemistry (Weinheim an der Bergstrasse, Germany) · 2023
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. A spin-1 representation for dual-funnel energy landscapes.The Journal of chemical physics · 2018
    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

7 authors.

Julien Brioche†School of Chemistry, University of Manchester, Oxford Road, Manchester M13 9PL, United Kingdom.
Sarah J Pike†School of Chemistry, University of Manchester, Oxford Road, Manchester M13 9PL, United Kingdom.
Sofja Tshepelevitsh‡Institute of Chemistry, University of Tartu, Ravila 14a, Tartu 50411, Estonia.
Ivo Leito‡Institute of Chemistry, University of Tartu, Ravila 14a, Tartu 50411, Estonia.
Gareth A Morris†School of Chemistry, University of Manchester, Oxford Road, Manchester M13 9PL, United Kingdom.
Simon J Webb†School of Chemistry, University of Manchester, Oxford Road, Manchester M13 9PL, United Kingdom.
Jonathan Clayden†School of Chemistry, University of Manchester, Oxford Road, Manchester M13 9PL, United Kingdom.

Funding

Biotechnology and Biological Sciences Research Council I007962
6 · The paper itself

Abstract

Biomolecular systems are able to respond to their chemical environment through reversible, selective, noncovalent intermolecular interactions. Typically, these interactions induce conformational changes that initiate a signaling cascade, allowing the regulation of biochemical pathways. In this work, we describe an artificial molecular system that mimics this ability to translate selective noncovalent interactions into reversible conformational changes. An achiral but helical foldamer carrying a basic binding site interacts selectively with the most acidic member of a suite of chiral ligands. As a consequence of this noncovalent interaction, a global absolute screw sense preference, detectable by (13)C NMR, is induced in the foldamer. Addition of base, or acid, to the mixture of ligands competitively modulates their interaction with the binding site, and reversibly switches the foldamer chain between its left and right-handed conformations. As a result, the foldamer-ligand mixture behaves as a biomimetic chemical system with emergent properties, functioning as a "proton-counting" molecular device capable of providing a tunable, pH-dependent conformational response to its environment.

Indexed as

Binding SitesBiomimetic MaterialsHydrogen-Ion ConcentrationLigandsMolecular ConformationMolecular StructureLigands

Identifiers

PMID25915163
PMCPMC4520694

What OpenQuestion holds

Textmetadata
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.