A Photoacoustic Contrast Agent for miR-21 via NIR Fluorescent Hybridization Chain Reaction.


Journal

Bioconjugate chemistry
ISSN: 1520-4812
Titre abrégé: Bioconjug Chem
Pays: United States
ID NLM: 9010319

Informations de publication

Date de publication:
15 06 2022
Historique:
pubmed: 19 8 2021
medline: 18 6 2022
entrez: 18 8 2021
Statut: ppublish

Résumé

Nucleic acids are well-established biomarkers of cancer with immense value in diagnostics and basic research. However, strategies to monitor these species in tissue can be challenging due to the need for amplification of imaging signal from low analyte concentrations with high specificity. Photoacoustic (PA) imaging is gaining traction for molecular imaging of proteins, small biomolecules, and nucleic acids by coupling pulsed near-infrared (NIR) excitation with broadband acoustic detection. This work introduces a PA nucleic acid contrast agent that harnesses NIR fluorophore and quencher-tagged hybridization chain reaction (HCR) for signal amplification. This HCR probe was designed to enable contact quenching between NIR dye-quencher pairs by coercing their direct alignment when miR-21, a microRNA cancer biomarker, is detected. The probe demonstrated a ratiometric PA limit of detection of 148 pM miR-21, sequence specificity against one- and two-base mutations, and selectivity over other microRNAs. It was further tested in live human ovarian cancer (SKOV3) and noncancerous (HEK 293T) cells to exemplify

Identifiants

pubmed: 34406744
doi: 10.1021/acs.bioconjchem.1c00375
pmc: PMC9122088
mid: NIHMS1803436
doi:

Substances chimiques

Contrast Media 0
Fluorescent Dyes 0
MIRN21 microRNA, human 0
MicroRNAs 0
DNA 9007-49-2

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1080-1092

Subventions

Organisme : NHLBI NIH HHS
ID : DP2 HL137187
Pays : United States
Organisme : NIAID NIH HHS
ID : R21 AI157957
Pays : United States
Organisme : NIH HHS
ID : S10 OD021821
Pays : United States
Organisme : NCI NIH HHS
ID : T32 CA153915
Pays : United States

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Auteurs

Raina M Borum (RM)

Department of NanoEngineering, University of California, San Diego, La Jolla, California 92093. United States.

Colman Moore (C)

Department of NanoEngineering, University of California, San Diego, La Jolla, California 92093. United States.

Soo Khim Chan (SK)

Department of NanoEngineering, University of California, San Diego, La Jolla, California 92093. United States.

Nicole F Steinmetz (NF)

Department of NanoEngineering, University of California, San Diego, La Jolla, California 92093. United States.
Department of Radiology, University of California, San Diego, La Jolla, California 92093. United States.
Department of Bioengineering, University of California, San Diego, La Jolla, California 92093. United States.
Center for Nano-ImmunoEngineering, University of California, San Diego, La Jolla, California 92093. United States.
Institute for Materials Discovery and Design, University of California, San Diego, La Jolla, California 92093. United States.
Moores Cancer Center, University of California, San Diego, La Jolla, California 92037. United States.

Jesse V Jokerst (JV)

Department of NanoEngineering, University of California, San Diego, La Jolla, California 92093. United States.
Materials Science and Engineering Program, University of California, San Diego, La Jolla, California 92093. United States.
Department of Radiology, University of California, San Diego, La Jolla, California 92093. United States.

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