Skip to main navigation Skip to search Skip to main content

Direct incorporation and extension of a fluorescent nucleotide through rolling circle DNA amplification for the detection of microRNA 24-3P

Research output: Contribution to journalJournal articlepeer-review

Abstract

We designed and synthesized several fluorescent nucleotides from thiophene, anthracene and pyrene, which have different sizes, and screened their incorporation and extension capability during the rolling circle amplification of DNA. The thiophene-based fluorescent nucleotide (dUthioTP) could highly incorporate and extended into the rolling circle DNA product, while other fluorescent nucleotides (dUanthTP, and dUpyrTP) could not. This dUthioTP fluorescent nucleotide could be used for the detection of miRNA 24-3P, which is related PRRSV. This direct labeling system during rolling circle DNA amplification exhibited an increased fluorescence signal showing gel formation for the detection of miRNA 24-3P. This direct labeling system is a very simple and cost-efficient method for the detection miRNA 24-3P and also exhibited highly sensitive and selective detection properties.

Original languageEnglish
Pages (from-to)2035-2038
Number of pages4
JournalBioorganic and Medicinal Chemistry Letters
Volume28
Issue number11
DOIs
StatePublished - 2018.06.15

Keywords

  • Direct labeling
  • Fluorescent nucleotide
  • miRNA
  • RCA
  • Virus

Quacquarelli Symonds(QS) Subject Topics

  • Medicine
  • Engineering - Petroleum
  • Pharmacy & Pharmacology
  • Chemistry
  • Biological Sciences

Fingerprint

Dive into the research topics of 'Direct incorporation and extension of a fluorescent nucleotide through rolling circle DNA amplification for the detection of microRNA 24-3P'. Together they form a unique fingerprint.

Cite this