Evidence map›Paper›PMID 39576313›Full record

ArticleAnalytical and bioanalytical chemistry2025

SERS-based CRISPR/Cas12a assays for protein biomarker prostate-specific antigen detection.

Peijun Teng, Zhixing Gao, Qiang Quan, Guangbo He, Qifang Song, Xiaoli Zhang, Wei Xiao, Jianfu Zhao, Donglin Cao, Jiajie Liang and 1 more

Abstract read
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In one paragraph

Article in Analytical and bioanalytical chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

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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

11 authors.

Peijun Teng *GuangDong Engineering Technology Research Center of Antibody Drug and Immunoassay, Department of Biological Sciences and Biotechnology, College of Life Science and Technology, Jinan University, Guangzhou, 510632, China.
Zhixing Gao *GuangDong Engineering Technology Research Center of Antibody Drug and Immunoassay, Department of Biological Sciences and Biotechnology, College of Life Science and Technology, Jinan University, Guangzhou, 510632, China.
Qiang Quan *Research Center of Cancer Diagnosis and Therapy, Department of Oncology, the First Affiliated Hospital, Jinan University, Guangzhou, 510632, China.
Guangbo HeGuangdong Zhongxin Biotech Limited, Guangzhou, 510000, China.
Qifang SongGuangDong Engineering Technology Research Center of Antibody Drug and Immunoassay, Department of Biological Sciences and Biotechnology, College of Life Science and Technology, Jinan University, Guangzhou, 510632, China.
Xiaoli ZhangGuangDong Engineering Technology Research Center of Antibody Drug and Immunoassay, Department of Biological Sciences and Biotechnology, College of Life Science and Technology, Jinan University, Guangzhou, 510632, China.
Wei XiaoDepartment of Laboratory Medicine, Guangdong Second Provincial General Hospital, Guangzhou, 510317, China. xkevent@foxmail.com.
Jianfu ZhaoResearch Center of Cancer Diagnosis and Therapy, Department of Oncology, the First Affiliated Hospital, Jinan University, Guangzhou, 510632, China. zhaojianfu@jnu.edu.cn.
Donglin CaoDepartment of Laboratory Medicine, Guangdong Second Provincial General Hospital, Guangzhou, 510317, China. caodl@126.com.
Jiajie LiangResearch Center of Cancer Diagnosis and Therapy, Department of Oncology, the First Affiliated Hospital, Jinan University, Guangzhou, 510632, China. 631101522@qq.com.
Yong TangGuangDong Engineering Technology Research Center of Antibody Drug and Immunoassay, Department of Biological Sciences and Biotechnology, College of Life Science and Technology, Jinan University, Guangzhou, 510632, China. tyjaq7926@163.com.

Funding

GuangDong Basic and Applied Basic Research Foundation 2021A1515110GuangDong Basic and Applied Basic Research Foundation 2021A1515220067GuangDong Basic and Applied Basic Research Foundation No. 2022A1515110772Key-Area Research and Development Program of Guangdong Province No. 2022B1111020003Outstanding Innovative Talents Cultivation Funded Programs for Doctoral Students of Jinan University No. 2023CXB014the National Natural Science Foundation of China 82372099the National Natural Science Foundation of China No. 32301266the Technology Research Program of Guangzhou City 2023A03J0283the Technology Research Program of Guangzhou City 2024A03J1076the Technology Research Program of Guangzhou City No. 202201011351
6 · The paper itself

Abstract

Sensitive and accurate detection of protein biomarkers is crucial for disease diagnosis, especially for early diagnosis. Here, we describe surface-enhanced Raman scattering (SERS)-based CRISPR/Cas12a assays (S-CRISPR) for protein biomarker detection. Firstly, an S-CRISPR-driven enzyme-linked immunosorbent assay (S-CasLISA) was developed utilizing a capture antibody coated on a microplate to recognize the target and a detection antibody labeled with active DNA to trigger the activity of CRISPR/Cas12a. With this assay, we achieved detection of prostate-specific antigen (PSA) as models at the picogram level. The limit of detection (LoD) of S-CasLISA was 0.17 pg mL

Indexed as

Limit of DetectionProstate-Specific AntigenSpectrum Analysis, RamanBiomarkersBiomarkers, TumorBiosensing TechniquesCRISPR-Cas SystemsEnzyme-Linked Immunosorbent AssayHumansMaleBiomarkersBiomarkers, TumorProstate-Specific AntigenAptamerCRISPR/Cas12aEnzyme-linked immunosorbent assayProtein biomarker detection

Identifiers

PMID39576313

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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.