Evidence map›Paper›PMID 36509424›Full record

ArticleACS applied materials & interfaces2022

Multiplexed Detection of Molecular Interactions with DNA Origami Engineered Cells in 3D Collagen Matrices.

Melika Shahhosseini, Peter E Beshay, Ehsan Akbari, Niksa Roki, Christopher R Lucas, Alex Avendano, Jonathan W Song, Carlos E Castro

Open access · greenAbstract read
In one paragraph

Article in ACS applied materials & interfaces, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Melika ShahhosseiniDepartment of Mechanical and Aerospace Engineering, The Ohio State University, 201 West 19th Avenue, Columbus, Ohio 43210, United States.
Peter E BeshayDepartment of Mechanical and Aerospace Engineering, The Ohio State University, 201 West 19th Avenue, Columbus, Ohio 43210, United States.
Ehsan AkbariBiophysics Graduate Program, The Ohio State University, Columbus, Ohio 43210, United States.
Niksa RokiDepartment of Mechanical and Aerospace Engineering, The Ohio State University, 201 West 19th Avenue, Columbus, Ohio 43210, United States.
Christopher R LucasDepartment of Mechanical and Aerospace Engineering, The Ohio State University, 201 West 19th Avenue, Columbus, Ohio 43210, United States.ORCID 0000-0002-4296-8656
Alex AvendanoDepartment of Biomedical Engineering, The Ohio State University, Columbus, Ohio 43210, United States.
Jonathan W SongDepartment of Mechanical and Aerospace Engineering, The Ohio State University, 201 West 19th Avenue, Columbus, Ohio 43210, United States.ORCID 0000-0002-6991-5298
Carlos E CastroDepartment of Mechanical and Aerospace Engineering, The Ohio State University, 201 West 19th Avenue, Columbus, Ohio 43210, United States.ORCID 0000-0001-7023-6105
The Ohio State University · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
Biophysical-based approach for controlling blood vessel structure and functionR01HL141941 · NHLBI · OHIO STATE UNIVERSITY · PI CASTRO, CARLOS E., PRAKASH, SHAURYA · 2018 to 2021
$2.0M
NCI NIH HHS P30 CA016058NHLBI NIH HHS R01 HL141941
6 · The paper itself

Abstract

The interactions of cells with signaling molecules present in their local microenvironment maintain cell proliferation, differentiation, and spatial organization and mediate progression of diseases such as metabolic disorders and cancer. Real-time monitoring of the interactions between cells and their extracellular ligands in a three-dimensional (3D) microenvironment can inform detection and understanding of cell processes and the development of effective therapeutic agents. DNA origami technology allows for the design and fabrication of biocompatible and 3D functional nanodevices via molecular self-assembly for various applications including molecular sensing. Here, we report a robust method to monitor live cell interactions with molecules in their surrounding environment in a 3D tissue model using a microfluidic device. We used a DNA origami cell sensing platform (CSP) to detect two specific nucleic acid sequences on the membrane of B cells and dendritic cells. We further demonstrated real-time detection of biomolecules with the DNA sensing platform on the surface of dendritic cells in a 3D microfluidic tissue model. Our results establish the integration of live cells with membranes engineered with DNA nanodevices into microfluidic chips as a highly capable biosensor approach to investigate subcellular interactions in physiologically relevant 3D environments under controlled biomolecular transport.

Indexed as

NanostructuresNanotechnologyCell CommunicationCollagenDNANucleic Acid ConformationCollagenDNAcell membrane engineeringcell microenvironmentDNA nanotechnologyDNA origamisubcellular interactions

Identifiers

PMID36509424
PMCPMC9785045
OpenAlexW4312210338

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.