ArticleNature nanotechnology2017
Translation of rod-like template sequences into homochiral assemblies of stacked helical oligomers.
Article in Nature nanotechnology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.
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.
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.
Who cites it
17 citing papers in PubMed, 72 citations in OpenAlex.
- Design of an abiotic unimolecular three-helix bundle.Chemical science · 2025Article
- A pillar[5]arene-based planar chiral charge-transfer dye with enhanced circularly polarized luminescence and multiple responsive chiroptical changes.Chemical science · 2023Article
- Directing the Self-Assembly of Aromatic Foldamer Helices using Acridine Appendages and Metal Coordination.Chemistry (Weinheim an der Bergstrasse, Germany) · 2022Article
- Formation of supramolecular channels by reversible unwinding-rewinding of bis(indole) double helix via ion coordination.Nature communications · 2022Article
- Anion-coordination-driven single-double helix switching and chiroptical molecular switching based on oligoureas.Chemical science · 2022Article
- Double helical π-aggregate nanoarchitectonics for amplified circularly polarized luminescence.Nature communications · 2022Article
- Review
- Chiral assembly of organic luminogens with aggregation-induced emission.Chemical science · 2022Review
- Chirality transmission in macromolecular domains.Nature communications · 2022Article
- A versatile living polymerization method for aromatic amides.Nature chemistry · 2021Article
- Hierarchical communication of chirality for aromatic oligoamide sequences.Nature communications · 2021Article
- Sensing a binding event through charge transport variations using an aromatic oligoamide capsule.Chemical science · 2021Article
- Making Molecular and Macromolecular Helical Tubes: Covalent and Noncovalent Approaches.ACS omega · 2018Review
- Designing cooperatively folded abiotic uni- and multimolecular helix bundles.Nature chemistry · 2018Article
- Multi-dimensional charge transport in supramolecular helical foldamer assemblies.Chemical science · 2017Article
- Transmission of chirality through space and across length scales.Nature nanotechnology · 2017Review
- Supramolecular chemistry: Host in translation.Nature nanotechnology · 2017Article
Corrections and comments
- Commented on by
Authors and funding
6 authors at 1 institution in 1 country.
Funding
Abstract
At the molecular level, translation refers to the production of a new entity according to a template that has a different chemical composition. In this way, chemical information may be translated from one molecule to another. The process is useful to synthesize structures and thus functions that might be difficult to create otherwise, and it reaches exquisite levels of efficiency in biological systems, as illustrated by protein expression from mRNA templates or by the assembly of the tobacco mosaic virus capsid protein according to the length of its RNA. In synthetic systems, examples of template-directed syntheses are numerous, but general and versatile schemes in which a non-natural sequence actually encodes the information necessary to produce a different sequence are few and far from being optimized. Here we show a high-fidelity enzyme-free translation of long rod-like alkylcarbamate oligomers into well-defined sequences of stacked helical aromatic oligoamides. The features present in the rods, which include the number and distance between carbamate functions and stereogenic centres, template the self-assembly of complementary stacks of helices that each have a defined right (P) or left (M) handedness, length and single or double helicity. This process enables the production of very large (>20 kDa) abiotic artificial folded architectures (foldamers) that may, for example, serve as scaffolds to organize appended functional features at positions in space defined with atomic precision across nanometric distances.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.