Literature DB >> 16122721

Amplification of circularizable probes for the detection of target nucleic acids and proteins.

David Zhang1, Josephine Wu, Fei Ye, Tao Feng, Ivy Lee, Bingjiao Yin.   

Abstract

BACKGROUND: Circularizable oligonucleotide probe (C-probe) is a unique molecule that offers significant advantages over conventional probes.
METHODS: Closed circular structure can be formed through ligation of the juxtaposed ends of the C-probe after hybridization with a target, and subsequently locked onto its target through the helical turns formed between the complementary sequences of the target and the C-probe (padlock probe). Under isothermal condition, C-probe can be amplified by rolling circle amplification (RCA) to generate multimeric single-stranded DNA (ssDNA). This multimeric ssDNA can be further amplified by a ramification mechanism (RAM) through primer extension and downstream DNA displacement, resulting in an exponential amplification. Usually, an unbiased product is generated by either RCA or ramification amplification method (or RAM) due to the generic primers of C-probe and its localization onto DNA targets.
CONCLUSIONS: These advantages make C-probe amplification very useful for research and molecular diagnosis, especially in areas where other techniques were proved to be inadequate. The development of C-probe-based technologies offers a promising prospect for molecular diagnosis. The applications of C-probe, RCA, RAM, in situ detection, microarray, immunoassay, single nucleotide polymorphism, and whole genome amplification, etc. are discussed in this review.

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Year:  2005        PMID: 16122721     DOI: 10.1016/j.cccn.2005.05.039

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN: 0009-8981            Impact factor:   3.786


  6 in total

1.  Rapid and direct microRNA quantification by an enzymatic luminescence assay.

Authors:  Ye Sun; Kalvin J Gregory; Nelson G Chen; Val Golovlev
Journal:  Anal Biochem       Date:  2012-07-01       Impact factor: 3.365

2.  Fluorescence imaging of single-copy DNA sequences within the human genome using PNA-directed padlock probe assembly.

Authors:  Anastasia I Yaroslavsky; Irina V Smolina
Journal:  Chem Biol       Date:  2013-03-21

3.  Simultaneous genotyping of all hemagglutinin and neuraminidase subtypes of avian influenza viruses by use of padlock probes.

Authors:  Péter Gyarmati; Tim Conze; Siamak Zohari; Neil LeBlanc; Mats Nilsson; Ulf Landegren; Johan Banér; Sándor Belák
Journal:  J Clin Microbiol       Date:  2008-03-19       Impact factor: 5.948

4.  Microsphere-based rolling circle amplification microarray for the detection of DNA and proteins in a single assay.

Authors:  Tania Konry; Ryan B Hayman; David R Walt
Journal:  Anal Chem       Date:  2009-07-15       Impact factor: 6.986

5.  Highly sensitive and specific screening of EGFR mutation using a PNA microarray-based fluorometric assay based on rolling circle amplification and graphene oxide.

Authors:  Xiaojun Xu; Shu Xing; Mengjia Xu; Pan Fu; Tingting Gao; Xiaokang Zhang; Yang Zhao; Chao Zhao
Journal:  RSC Adv       Date:  2019-11-22       Impact factor: 4.036

6.  Labeling of unique sequences in double-stranded DNA at sites of vicinal nicks generated by nicking endonucleases.

Authors:  Heiko Kuhn; Maxim D Frank-Kamenetskii
Journal:  Nucleic Acids Res       Date:  2008-03-15       Impact factor: 16.971

  6 in total

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