Evidence map›Paper›PMID 36355575›Full record

ArticleThe journal of physical chemistry letters2022

Exciton Chirality Inversion in Dye Dimers Templated by DNA Holliday Junction.

Olga A Mass, Shibani Basu, Lance K Patten, Ewald A Terpetschnig, Alexander I Krivoshey, Anatoliy L Tatarets, Ryan D Pensack, Bernard Yurke, William B Knowlton, Jeunghoon Lee

Abstract read
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Article in The journal of physical chemistry letters, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

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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

5 citing papers in PubMed.

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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

10 authors.

Ewald A TerpetschnigSETA BioMedicals, LLC, 2014 Silver Court East, Urbana, Illinois 61801, United States.
Alexander I KrivosheySSI "Institute for Single Crystals" of the National Academy of Sciences of Ukraine, 60 Nauky Ave., 61072 Kharkiv, Ukraine.
Anatoliy L TataretsSSI "Institute for Single Crystals" of the National Academy of Sciences of Ukraine, 60 Nauky Ave., 61072 Kharkiv, Ukraine.ORCID 0000-0003-4406-7883
William B KnowltonORCID 0000-0003-3018-2207

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

While only one enantiomer of chiral biomolecules performs a biological function, access to both enantiomers (or enantiomorphs) proved to be advantageous for technology. Using dye covalent attachment to a DNA Holliday junction (HJ), we created two pairs of dimers of bis(chloroindolenine)squaraine dye that enabled strongly coupled molecular excitons of opposite chirality in solution. The exciton chirality inversion was achieved by interchanging single covalent linkers of unequal length tethering the dyes of each dimer to the HJ core. Dimers in each pair exhibited profound exciton-coupled circular dichroism (CD) couplets of opposite signs. Dimer geometries, modeled by simultaneous fitting absorption and CD spectra, were related in each pair as nonsuperimposable and nearly exact mirror images. The origin of observed exciton chirality inversion was explained in the view of isomerization of the stacked Holliday junction. This study will open new opportunities for creating excitonic DNA-based materials that rely on programmable system chirality.

Indexed as

Coloring AgentsDNA, CruciformCircular DichroismDNAStereoisomerismColoring AgentsDNADNA, Cruciform

Identifiers

PMID36355575
PMCPMC9706552

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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.