Evidence map›Paper›PMID 38690801›Full record

ArticleLangmuir : the ACS journal of surfaces and colloids2024

Minimizing Structural Heterogeneity in DNA Self-Assembled Dye Templating via DNA Origami-Tuned Conformations.

Keitel Cervantes-Salguero, Madison Kadrmas, Brett M Ward, Drew Lysne, Amanda Wolf, Luca Piantanida, Gissela Pascual, William B Knowlton

Open access · hybridAbstract read
In one paragraph

Article in Langmuir : the ACS journal of surfaces and colloids, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
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

8 authors at 2 institutions in 1 country.

Keitel Cervantes-SalgueroMicron School of Materials Science and Engineering, Boise State University, Boise, Idaho 83725, United States.ORCID 0000-0001-8834-8711
Madison KadrmasMicron School of Materials Science and Engineering, Boise State University, Boise, Idaho 83725, United States.ORCID 0000-0002-8466-5434
Brett M WardMicron School of Materials Science and Engineering, Boise State University, Boise, Idaho 83725, United States.
Drew LysneMicron School of Materials Science and Engineering, Boise State University, Boise, Idaho 83725, United States.ORCID 0000-0001-6007-6478
Amanda WolfBiomolecular Sciences Graduate Programs, Boise State University, Boise, Idaho 83725, United States.
Luca PiantanidaMicron School of Materials Science and Engineering, Boise State University, Boise, Idaho 83725, United States.
Gissela PascualMicron School of Materials Science and Engineering, Boise State University, Boise, Idaho 83725, United States.
William B KnowltonMicron School of Materials Science and Engineering, Boise State University, Boise, Idaho 83725, United States.ORCID 0000-0003-3018-2207
Micron (United States) · USBoise State University · US

Funding

XRAY CRYSTALLOGRAPHIC STRUCTURE ANALYSIS: PROTEIN SORTINGP41RR001081 · NCRR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GODDARD, THOMAS · 1985 to 2011
$17.6M
NCRR NIH HHS P41 RR001081
6 · The paper itself

Abstract

With recent advances in DNA-templated dye aggregation for leveraging and engineering molecular excitons, a need exists for minimizing structural heterogeneity. Holliday Junction complexes (HJ) are commonly used to covalently template dye aggregates on their core; however, the global conformation of HJ is detrimentally dynamic. Here, the global conformation of the HJ is selectively tuned by restricting its position and orientation by using a sheet-like DNA origami construct (DOC) physisorbed on glass. The HJ arms are fixed with four different designed interduplex angles (IDAs). Atomic force microscopy confirmed that the HJs are bound to the surface of DOC with tuned IDAs. Dye orientation distributions were determined by combining dipole imaging and super-resolution microscopy. All IDAs led to dye orientations having dispersed distributions along planes perpendicular to the HJ plane, suggesting that stacking occurred between the dye and the neighboring DNA bases. The dye-base stacking interpretation was supported by increasing the size of the core cavity. The narrowest IDA minimizes structural heterogeneity and suggests dye intercalation. A strong correlation is found between the IDA and the orientation of the dye along the HJ plane. These results show that the HJ imposes restrictions on the dye and that the dye-DNA interactions are always present regardless of global conformation. The implications of our results are discussed for the scalability of dye aggregates using DNA self-assembly. Our methodology provides an avenue for the solid-supported single-molecule characterization of molecular assemblies templated on biomolecules─such as DNA and protein templates involved in light-harvesting and catalysis─with tuned conformations and restricted in position and orientation.

Indexed as

DNA, CruciformNucleic Acid ConformationColoring AgentsDNAMicroscopy, Atomic ForceColoring AgentsDNADNA, Cruciform

Identifiers

PMID38690801
PMCPMC11100016
OpenAlexW4396554612

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.