Evidence map›Paper›PMID 39475291›Full record

ArticleJournal of the American Chemical Society2024

Directing Nanoparticle Organization in Response to Diverse Chemical Inputs.

Yan Xiong, Colin Yancey, Heon-Joon Lee, Dayoung Gloria Lee, Emily Helm, Byunghwa Kang, Alison Grinthal, Daniel McKeen, Oleg Gang, Rebecca Schulman

Erratum issuedAbstract read
In one paragraph

Article in Journal of the American Chemical Society, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Dynamic Control of DNA Origami Self-Assembly by Transcriptional Modules.Journal of the American Chemical Society · 2026
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Yan XiongInstitute for Nanobiotechnology, Johns Hopkins University, Baltimore, Maryland 21218, United States.
Colin YanceyDepartment of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, Maryland 21218, United States.
Heon-Joon LeeDepartment of Biomedical Engineering, Johns Hopkins University School of Medicine, Baltimore, Maryland 21218, United States.
Dayoung Gloria LeeDepartment of Chemical Engineering, Columbia University, New York, New York 10027, United States.ORCID 0000-0002-3956-0203
Emily HelmDepartment of Chemistry, Johns Hopkins University School of Medicine, Baltimore, Maryland 21218, United States.
Byunghwa KangInstitute for Nanobiotechnology, Johns Hopkins University, Baltimore, Maryland 21218, United States.
Alison GrinthalInstitute for Nanobiotechnology, Johns Hopkins University, Baltimore, Maryland 21218, United States.
Daniel McKeenDepartment of Chemical Engineering, Columbia University, New York, New York 10027, United States.
Oleg GangDepartment of Chemical Engineering, Columbia University, New York, New York 10027, United States.ORCID 0000-0001-5534-3121
Rebecca SchulmanInstitute for Nanobiotechnology, Johns Hopkins University, Baltimore, Maryland 21218, United States.ORCID 0000-0003-4555-3162

Funding

The Chemistry-Biology Interface Program at Johns Hopkins UniversityT32GM080189 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI ROKITA, STEVEN E · 2008 to 2022
$3.5M
The Chemistry-Biology Interface Program at Johns Hopkins UniversityT32GM149382 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI STEVEN E ROKITA · 2023 to 2026
$1.4M
Secretion responsive Hydrogels for Identification of Functional single T cells (SHIFT)R21CA251027 · NCI · JOHNS HOPKINS UNIVERSITY · PI SCHULMAN, REBECCA · 2021 to 2023
$565k
NCI NIH HHS R21 CA251027NIGMS NIH HHS T32 GM080189NIGMS NIH HHS T32 GM149382
6 · The paper itself

Abstract

Signaling cascades are crucial for transducing stimuli in biological systems, enabling multiple stimuli to regulate a downstream target with precisely controlled timing and amplifying signals through a series of intermediary reactions. Developing a robust signaling system with such capabilities would be pivotal for programming complex behaviors in synthetic DNA-based molecular devices. However, although "software" such as nucleic acid circuits could potentially be harnessed to relay signals to DNA-based nanostructure hardware, such explorations have been limited. Here, we develop a platform for transducing a variety of stimuli via messenger-mediated reactions to regulate the release and reloading of gold nanoparticles (AuNPs) in a 3D DNA framework. In the first step, an in vitro transcription circuit is engineered to sense and amplify chemical stimuli, including arbitrary DNA sequences and proteins, producing RNA. In the second step, the RNA releases the DNA-coated AuNPs from the DNA framework via a strand displacement reaction. AuNP reloading is controlled by a separate step driven by degradation of the RNA. Our platform holds promise for applications requiring dynamic multiagent control over DNA-based devices, offering a versatile tool for advanced molecular device engineering.

Indexed as

DNAGoldMetal NanoparticlesRNADNAGoldRNA

Identifiers

PMID39475291
PMCPMC11613787

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.