Evidence map›Paper›PMID 39419834›Full record

ArticleAnalytical and bioanalytical chemistry2024

Enzyme-free immunoassay for rapid, sensitive, and selective detection of C-reactive protein.

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

Abstract read
In one paragraph

Article in Analytical and bioanalytical chemistry, 2024. 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
–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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Regulation of Protein Transport in Functionalized PET Nanopores.The journal of physical chemistry. B · 2025
    Article
  6. Article
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.
Haiyan ZhengDepartment of Chemistry, University of Missouri, Columbia, MO, 65211, USA.
Rana JahaniDepartment of Chemistry, University of Missouri, Columbia, MO, 65211, USA.
Shuo ZhouDepartment of Chemistry, University of Missouri, Columbia, MO, 65211, USA.
Jun ChenDepartment of Chemistry, University of Missouri, Columbia, MO, 65211, USA.
Juanhua KongDepartment of Chemistry, University of Missouri, Columbia, MO, 65211, USA.
Xiyun GuanDepartment of Chemistry, University of Missouri, Columbia, MO, 65211, USA. xgpc2@missouri.edu.ORCID http://orcid.org/0000-0003-2022-4872

Funding

Solid-state nanopore detection of protein biomarkers for early sepsisdiagnosisR01GM147247 · NIGMS · UNIVERSITY OF MISSOURI-COLUMBIA · PI GUAN, XIYUN · 2022 to 2025
$1.2M
Division of Chemistry 2203763Division of Chemistry 2345813NIGMS NIH HHS R01 GM147247NIGMS NIH HHS R01GM147247
6 · The paper itself

Abstract

C-reactive protein (CRP) is a protein made by the liver, which is released into the bloodstream in response to inflammation. Furthermore, CRP is a potential risk factor for heart disease. Hence, it is of great importance to develop a rapid, sensitive, accurate, and cost-effective method for CRP detection. Herein, we report an enzyme-free fluorescent assay for the rapid and ultra-sensitive detection of CRP with a limit of detection (LOD) reaching as low as 3.08 pg/mL (i.e., ~ 27 fM). The high sensitivity of our method was simply achieved via dual-functionalized gold nanoparticles (AuNPs). By regulating the molar ratio of DNA to CRP antibody immobilized on the AuNP surface, hundreds to thousands-fold amplification in the analyte signal could be instantly accomplished. Furthermore, our sensor was selective: non-target proteins such as interleukin-6, interleukin-1β, procalcitonin, bovine serum albumin, and human serum albumin did not interfere with the target CRP detection. Moreover, simulated serum samples were successfully analyzed. Given the excellent sensitivity, selectivity, and high resistance to complicated matrices, the enzyme-free CRP detection strategy developed in this work can be used as a generic platform to construct sensors for a wide variety of protein biomarkers and hence offers potential as a tool for rapid, accurate, and low-cost medical diagnosis.

Indexed as

C-Reactive ProteinGoldLimit of DetectionMetal NanoparticlesAntibodies, ImmobilizedBiosensing TechniquesHumansImmunoassayAntibodies, ImmobilizedC-Reactive ProteinGoldAmplificationAuNPsCRP proteinEnzyme-free immunoassayFluorescent assay

Identifiers

PMID39419834
PMCPMC12007592

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Registered trials

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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.