Evidence map›Paper›PMID 34062334›Full record

ArticleBiosensors & bioelectronics2021

Electrophoretic mobility shift as a molecular beacon-based readout for miRNA detection.

Getulio P Oliveira-Jr, Raquel H Barbosa, Lauren Thompson, Brandy Pinckney, Moriah Murphy-Thornley, Shulin Lu, Jennifer Jones, Clinton H Hansen, John Tigges, Wesley P Wong and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Biosensors & bioelectronics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

4 citing papers in PubMed, 12 citations in OpenAlex.

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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 at 3 institutions in 1 country.

Getulio P Oliveira-JrDivision of Allergy and Inflammation, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, United States. Electronic address: gpereira@bidmc.harvard.edu.
Raquel H BarbosaDivision of Allergy and Inflammation, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, United States.
Lauren ThompsonNano Flow Core Facility, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, United States.
Brandy PinckneyNano Flow Core Facility, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, United States.
Moriah Murphy-ThornleyDivision of Allergy and Inflammation, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, United States.
Shulin LuDivision of Allergy and Inflammation, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, United States.
Jennifer JonesLaboratory of Pathology Center for Cancer Research, National Cancer Institute, Bethesda, MD, United States.
Clinton H HansenProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Department of Biological Chemistry and Molecular Pharmacology, Blavatnik Institute, Harvard Medical School, Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02115, USA.
John TiggesNano Flow Core Facility, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, United States.
Wesley P WongProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Department of Biological Chemistry and Molecular Pharmacology, Blavatnik Institute, Harvard Medical School, Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02115, USA.
Ionita C GhiranDivision of Allergy and Inflammation, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, United States. Electronic address: ighiran@bidmc.harvard.edu.
Beth Israel Deaconess Medical Center · USBoston Children's Hospital · USNational Cancer Institute · US

Funding

Mechanical forces in nanoscale biology: From hemostasis to single-molecule centrifugationR35GM119537 · NIGMS · BOSTON CHILDREN'S HOSPITAL · PI Wesley Philip Wong · 2016 to 2026
$5.2M
Effect of methodological and biological variability on molecular profiling of extracellular vesicles in cancer detectionR01CA218500 · NCI · NORTHEASTERN UNIVERSITY · PI GHIRAN, IONITA CALIN, IVANOV, ALEXANDER R. · 2018 to 2022
$4.0M
Bioengineered red blood cells as extracellular vesicle-mediated delivery platforms for gene editing machineryUG3HL147353 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI GHIRAN, IONITA CALIN · 2018 to 2020
$2.4M
Integrative, multi-parametric characterization of the EV surface protein and nucleic acid landscape by nano-flow and sorting cytometryUH3TR002881 · NCATS · BETH ISRAEL DEACONESS MEDICAL CENTER · PI GHIRAN, IONITA CALIN, JONES, JENNIFER · 2021 to 2022
$1.9M
Integrative, multi-parametric characterization of the EV surface protein and nucleic acid landscape by nano-flow and sorting cytometryUG3TR002881 · NCATS · BETH ISRAEL DEACONESS MEDICAL CENTER · PI GHIRAN, IONITA CALIN, JONES, JENNIFER · 2019 to 2020
$816k
NCATS NIH HHS UG3 TR002881NCATS NIH HHS UH3 TR002881NCI NIH HHS R01 CA218500NHLBI NIH HHS UG3 HL147353NIGMS NIH HHS R35 GM119537
6 · The paper itself

Abstract

MicroRNAs are short, non-coding RNA sequences involved in gene expression regulation. Quantification of miRNAs in biological fluids involves time consuming and laborious methods such as Northern blotting or PCR-based techniques. Molecular beacons (MB) are an attractive means for rapid detection of miRNAs, although the need for sophisticated readout methods limits their use in research and clinical settings. Here, we introduce a novel method based on delayed electrophoretic mobility, as a quantitative means for detection of miRNAs-MB hybridization. Upon hybridization with the target miRNAs, MB form a fluorescent duplex with reduced electrophoretic mobility, thus bypassing the need for additional staining. In addition to emission of light, the location of the fluorescent band on the gel acts as an orthogonal validation of the target identity, further confirming the specificity of binding. The limit of detection of this approach is approximately 100 pM, depending on the MB sequence. The method is sensitive enough to detect specific red blood cell miRNAs molecules in total RNA, with single nucleotide specificity. Altogether, we describe a rapid and affordable method that offers sensitive detection of single-stranded small DNA and RNA sequences.

Indexed as

Biosensing TechniquesMicroRNAsGene Expression RegulationNucleic Acid HybridizationMicroRNAsElectrophoretic mobilityGel electrophoresismicroRNA (miRNA)Molecular beacons

Identifiers

PMID34062334
PMCPMC8461749
OpenAlexW3160095575

What OpenQuestion holds

Textmetadata
LicenceTDM
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.