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HERO ID
7614282
Reference Type
Journal Article
Title
Direct incorporation and extension of a fluorescent nucleotide through rolling circle DNA amplification for the detection of microRNA 24-3P
Author(s)
Le, BH; Seo, YJ; ,
Year
2018
Is Peer Reviewed?
Yes
Journal
Bioorganic & Medicinal Chemistry Letters
ISSN:
0960-894X
EISSN:
1464-3405
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Location
OXFORD
Volume
28
Issue
11
Page Numbers
2035-2038
Language
English
PMID
29709251
DOI
10.1016/j.bmcl.2018.04.058
Web of Science Id
WOS:000432876000010
URL
https://linkinghub.elsevier.com/retrieve/pii/S0960894X18303706
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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.
Keywords
Direct labeling; Fluorescent nucleotide; miRNA; RCA; Virus
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