Evidence map›Paper›PMID 42016216›Full record

ArticleMaterials advances2026

A CRISPR-Cas12a amplified RNase activity sensor powered by gold nanoparticle-barcode DNA multipliers.

Sathishkumar Munusamy, Rana Jahani, Jun Chen, Shuo Zhou, Juanhua Kong, Haiyan Zheng, Xiyun Guan

Abstract read
In one paragraph

Article in Materials advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Sathishkumar MunusamyDepartment of Chemistry, University of Missouri Columbia MO 65211 USA haiyanzheng1111@gmail.com xgpc2@missouri.edu.ORCID https://orcid.org/0000-0002-4776-3318
Rana JahaniDepartment of Chemistry, University of Missouri Columbia MO 65211 USA haiyanzheng1111@gmail.com xgpc2@missouri.edu.ORCID https://orcid.org/0009-0009-8896-320X
Jun ChenDepartment of Chemistry, University of Missouri Columbia MO 65211 USA haiyanzheng1111@gmail.com xgpc2@missouri.edu.ORCID https://orcid.org/0009-0007-2951-0978
Shuo ZhouDepartment of Chemistry, University of Missouri Columbia MO 65211 USA haiyanzheng1111@gmail.com xgpc2@missouri.edu.ORCID https://orcid.org/0000-0002-7491-3983
Juanhua KongDepartment of Chemistry, University of Missouri Columbia MO 65211 USA haiyanzheng1111@gmail.com xgpc2@missouri.edu.
Haiyan ZhengDepartment of Chemistry, University of Missouri Columbia MO 65211 USA haiyanzheng1111@gmail.com xgpc2@missouri.edu.ORCID https://orcid.org/0009-0005-0658-1437
Xiyun GuanDepartment of Chemistry, University of Missouri Columbia MO 65211 USA haiyanzheng1111@gmail.com xgpc2@missouri.edu.ORCID https://orcid.org/0000-0003-2022-4872

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ribonuclease A (RNase A) is a clinically relevant biomarker whose aberrant activity compromises RNA stability and interferes with RNA-based therapeutics, highlighting the need for rapid and ultrasensitive detection tools. In this work, we developed a CRISPR/Cas12a-assisted biosensing platform integrated with a substrate-bridged magnetic bead-gold nanoparticle assembly (SB-MAC) for highly sensitive and selective RNase A detection. By optimizing AuNP loading density, RNA substrate/barcode DNA molar ratio, and enzymatic incubation conditions, the prepared dual-functionalized SB-MAC architecture enabled efficient substrate/RNase A cleavage interaction and significant signal amplification, yielding a limit of detection (LOD) of 0.16 pg mL

Identifiers

PMID42016216
PMCPMC13093252

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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.