Evidence map›Paper›PMID 34163977›Full record

ArticleChemical science2021

Amplified detection of nucleic acids and proteins using an isothermal proximity CRISPR Cas12a assay.

Yongya Li, Hayam Mansour, Colton J F Watson, Yanan Tang, Adam J MacNeil, Feng Li

Open access · diamondAbstract read
In one paragraph

Article in Chemical science, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
5.3field-weighted citation impact, top 3% of its field
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

20 citing papers in PubMed, 85 citations in OpenAlex.

  1. Review
  2. Article
  3. Advances in nanozyme-assisted CRISPR diagnostic technology.Frontiers in bioengineering and biotechnology · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Signal Amplification by theAnalytical chemistry · 2023
    Review
  14. Review
  15. Review
  16. Article
  17. The fluorescence amplification strategy based on 3D DNA walker and CRISPR/Cas12a for the rapid detection of BRAF V600E.Analytical sciences : the international journal of the Japan Society for Analytical Chemistry · 2022
    Article
  18. Next-Generation Diagnostic with CRISPR/Cas: Beyond Nucleic Acid Detection.International journal of molecular sciences · 2022
    Review
  19. Article
  20. 2'-Chemical science · 2022
    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

6 authors at 2 institutions in 6 countries.

Yongya LiKey Laboratory of Green Chemistry & Technology of Ministry of Education, College of Chemistry, Analytical & Testing Center, Sichuan University 29 Wangjing Road Chengdu Sichuan 610064 China yanantang@scu.edu.cn.
Hayam MansourDepartment of Chemistry, Centre for Biotechnology, Brock University St. Catharines Ontario L2S 3A1 Canada fli@brocku.ca.
Colton J F WatsonDepartment of Health Sciences, Brock University St. Catharines Ontario L2S 3A1 Canada.
Yanan TangKey Laboratory of Green Chemistry & Technology of Ministry of Education, College of Chemistry, Analytical & Testing Center, Sichuan University 29 Wangjing Road Chengdu Sichuan 610064 China yanantang@scu.edu.cn.
Adam J MacNeilDepartment of Health Sciences, Brock University St. Catharines Ontario L2S 3A1 Canada.
Feng LiKey Laboratory of Green Chemistry & Technology of Ministry of Education, College of Chemistry, Analytical & Testing Center, Sichuan University 29 Wangjing Road Chengdu Sichuan 610064 China yanantang@scu.edu.cn.ORCID https://orcid.org/0000-0002-2616-5343
Brock University · CASichuan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Herein, we describe an isothermal proximity CRISPR Cas12a assay that harnesses the target-induced indiscrimitive single-stranded DNase activity of Cas12a for the quantitative profiling of gene expression at the mRNA level and detection of proteins with high sensitivity and specificity. The target recognition is achieved through proximity binding rather than recognition by CRISPR RNA (crRNA), which allows for flexible assay design. A binding-induced primer extension reaction is used to generate a predesigned CRISPR-targetable sequence as a barcode for further signal amplification. Through this dual amplification protocol, we were able to detect as low as 1 fM target nucleic acid and 100 fM target protein isothermally. The practical applicability of this assay was successfully demonstrated for the temporal profiling of interleukin-6 gene expression during allergen-mediated mast cell activation.

Identifiers

PMID34163977
PMCPMC8179305
OpenAlexW3120114060

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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 OpenQuestion graph.