A low-cost fluorescence reader for in vitro transcription and nucleic acid detection with Cas13a.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2019
Historique:
received: 05 07 2019
accepted: 22 10 2019
entrez: 19 12 2019
pubmed: 19 12 2019
medline: 25 3 2020
Statut: epublish

Résumé

Point-of-care testing (POCT) in low-resource settings requires tools that can operate independently of typical laboratory infrastructure. Due to its favorable signal-to-background ratio, a wide variety of biomedical tests utilize fluorescence as a readout. However, fluorescence techniques often require expensive or complex instrumentation and can be difficult to adapt for POCT. To address this issue, we developed a pocket-sized fluorescence detector costing less than $15 that is easy to manufacture and can operate in low-resource settings. It is built from standard electronic components, including an LED and a light dependent resistor, filter foils and 3D printed parts, and reliably reaches a lower limit of detection (LOD) of ≈ 6.8 nM fluorescein, which is sufficient to follow typical biochemical reactions used in POCT applications. All assays are conducted on filter paper, which allows for a flat detector architecture to improve signal collection. We validate the device by quantifying in vitro RNA transcription and also demonstrate sequence-specific detection of target RNAs with an LOD of 3.7 nM using a Cas13a-based fluorescence assay. Cas13a is an RNA-guided, RNA-targeting CRISPR effector with promiscuous RNase activity upon recognition of its RNA target. Cas13a sensing is highly specific and adaptable and in combination with our detector represents a promising approach for nucleic acid POCT. Furthermore, our open-source device may be used in educational settings, through providing low cost instrumentation for quantitative assays or as a platform to integrate hardware, software and biochemistry concepts in the future.

Identifiants

pubmed: 31851676
doi: 10.1371/journal.pone.0220091
pii: PONE-D-19-18880
pmc: PMC6919979
doi:

Substances chimiques

Bacterial Proteins 0
CRISPR-Associated Proteins 0
RNA, Bacterial 0
Green Fluorescent Proteins 147336-22-9

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0220091

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Florian Katzmeier (F)

Physics Department and ZNN, Technical University of Munich, Garching, Germany.

Lukas Aufinger (L)

Physics Department and ZNN, Technical University of Munich, Garching, Germany.

Aurore Dupin (A)

Physics Department and ZNN, Technical University of Munich, Garching, Germany.

Jorge Quintero (J)

Department of Biology, Ludwig-Maximilians-Universität Munich, Martinsried, Germany.

Matthias Lenz (M)

Physics Department and ZNN, Technical University of Munich, Garching, Germany.

Ludwig Bauer (L)

Physics Department and ZNN, Technical University of Munich, Garching, Germany.

Sven Klumpe (S)

Physics Department and ZNN, Technical University of Munich, Garching, Germany.

Dawafuti Sherpa (D)

Department of Biology, Ludwig-Maximilians-Universität Munich, Martinsried, Germany.

Benedikt Dürr (B)

Department of Biology, Ludwig-Maximilians-Universität Munich, Martinsried, Germany.

Maximilian Honemann (M)

Physics Department and ZNN, Technical University of Munich, Garching, Germany.

Igor Styazhkin (I)

Physics Department and ZNN, Technical University of Munich, Garching, Germany.

Friedrich C Simmel (FC)

Physics Department and ZNN, Technical University of Munich, Garching, Germany.

Michael Heymann (M)

Intelligent Biointegrative Systems Group, Institute for Biomaterials and Biomolecular Systems, University Stuttgart, Germany.

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Classifications MeSH