Evidence map›Paper›PMID 35343100›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2022

A Highly Sensitive CRISPR-Empowered Surface Plasmon Resonance Sensor for Diagnosis of Inherited Diseases with Femtomolar-Level Real-Time Quantification.

Fei Zheng, Zhi Chen, Jingfeng Li, Rui Wu, Bin Zhang, Guohui Nie, Zhongjian Xie, Han Zhang

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing 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

40 citing papers in PubMed.

  1. Biophysical characterization ofSensors & diagnostics · 2026
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  10. Phototherapy in cancer treatment: strategies and challenges.Signal transduction and targeted therapy · 2025
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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.

Fei ZhengShenzhen Engineering Laboratory of phosphorene and Optoelectronics, International Collaborative Laboratory of 2D Materials for Optoelectronics Science and Technology of Ministry of Education, Shenzhen Institute of Translational Medicine, Department of Otolaryngology, Shenzhen Second People's Hospital, the First Affiliated Hospital, Institute of Microscale Optoelectronics, Shenzhen University, Shenzhen, 518060, P.R. China.
Zhi ChenShenzhen Engineering Laboratory of phosphorene and Optoelectronics, International Collaborative Laboratory of 2D Materials for Optoelectronics Science and Technology of Ministry of Education, Shenzhen Institute of Translational Medicine, Department of Otolaryngology, Shenzhen Second People's Hospital, the First Affiliated Hospital, Institute of Microscale Optoelectronics, Shenzhen University, Shenzhen, 518060, P.R. China.ORCID 0000-0002-7624-3143
Jingfeng LiShenzhen Engineering Laboratory of phosphorene and Optoelectronics, International Collaborative Laboratory of 2D Materials for Optoelectronics Science and Technology of Ministry of Education, Shenzhen Institute of Translational Medicine, Department of Otolaryngology, Shenzhen Second People's Hospital, the First Affiliated Hospital, Institute of Microscale Optoelectronics, Shenzhen University, Shenzhen, 518060, P.R. China.
Rui WuLaboratory of Robotics and System, Harbin Institute of Technology, Harbin, 150001, P. R. China.
Bin ZhangShenzhen Engineering Laboratory of phosphorene and Optoelectronics, International Collaborative Laboratory of 2D Materials for Optoelectronics Science and Technology of Ministry of Education, Shenzhen Institute of Translational Medicine, Department of Otolaryngology, Shenzhen Second People's Hospital, the First Affiliated Hospital, Institute of Microscale Optoelectronics, Shenzhen University, Shenzhen, 518060, P.R. China.
Guohui NieShenzhen Engineering Laboratory of phosphorene and Optoelectronics, International Collaborative Laboratory of 2D Materials for Optoelectronics Science and Technology of Ministry of Education, Shenzhen Institute of Translational Medicine, Department of Otolaryngology, Shenzhen Second People's Hospital, the First Affiliated Hospital, Institute of Microscale Optoelectronics, Shenzhen University, Shenzhen, 518060, P.R. China.
Zhongjian XieInstitute of Pediatrics, Shenzhen Children's Hospital, Shenzhen, Guangdong, 518038, P. R. China.
Han ZhangShenzhen Engineering Laboratory of phosphorene and Optoelectronics, International Collaborative Laboratory of 2D Materials for Optoelectronics Science and Technology of Ministry of Education, Shenzhen Institute of Translational Medicine, Department of Otolaryngology, Shenzhen Second People's Hospital, the First Affiliated Hospital, Institute of Microscale Optoelectronics, Shenzhen University, Shenzhen, 518060, P.R. China.ORCID 0000-0002-0166-1973

Funding

Guangdong Basic and Applied Basic Research Foundation 2019B1515120043Longhua District Science and Innovation Commission Project Grants of Shenzhen JCYJ201904Natural Science Foundation of Guangdong Province 2020A151501612Science and Technology Innovation Commission of Shenzhen KCXFZ20201221173413038The Science and Technology Project of Shenzhen JCYJ20180508152903208
6 · The paper itself

Abstract

The clustered regularly interspaced short palindromic repeats (CRISPR) molecular system has emerged as a promising technology for the detection of nucleic acids. Herein, the development of a surface plasmon resonance (SPR) sensor that is functionalized with a layer of locally grown graphdiyne film, achieving excellent sensing performance when coupled with catalytically deactivated CRISPR-associated protein 9 (dCas9), is reported. dCas9 protein is immobilized on the sensor surface and complexed with a specific single-guide RNA, enabling the amplification-free detection of target sequences within genomic DNA. The sensor, termed CRISPR-SPR-Chip, is used to successfully analyze recombinant plasmids with only three-base mutations with a limit of detection as low as 1.3 fM. Real-time monitoring CRISPR-SPR-Chip is used to analyze clinical samples of patients with Duchenne muscular dystrophy with two exon deletions, which are detected without any pre-amplification step, yielding significantly positive results within 5 min. The ability of this novel CRISPR-empowered SPR (CRISPR-eSPR) sensing platform to rapidly, precisely, sensitively, and specifically detect a target gene sequence provides a new on-chip optic approach for clinical gene analysis.

Indexed as

Clustered Regularly Interspaced Short Palindromic RepeatsNucleic AcidsCRISPR-Cas SystemsHumansRNA, Guide, CRISPR-Cas SystemsSurface Plasmon ResonanceNucleic AcidsRNA, Guide, CRISPR-Cas Systemsbiosensorclustered regularly interspaced short palindromic repeats (CRISPR)nucleic acid detectionsurface plasmon resonancetwo-dimensional materials

Identifiers

PMID35343100
PMCPMC9108660

What OpenQuestion holds

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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.