| Literature DB >> 25953623 |
Zunyi Yang1, Chris McLendon2, Daniel Hutter2,3, Kevin M Bradley2, Shuichi Hoshika2, Carole B Frye3, Steven A Benner4,5.
Abstract
Assays that detect DNA or RNA (xNA) are highly sensitive, as small amounts of xNA can be amplified by PCR. Unfortunately, PCR is inconvenient in low-resource environments, and requires equipment and power that might not be available in these environments. Isothermal procedures, which avoid thermal cycling, are often confounded by primer dimers, off-target priming, and other artifacts. Here, we show how a "self avoiding molecular recognition system" (SAMRS) eliminates these artifacts and gives clean amplicons in a helicase-dependent isothermal amplification (SAMRS-HDA). We also show that incorporating SAMRS into the 3'-ends of primers facilitates the design and screening of primers for HDA assays. Finally, we show that SAMRS-HDA can be twofold multiplexed, difficult to achieve with HDA using standard primers. Thus, SAMRS-HDA is a more versatile approach than standard HDA, with a broader applicability for xNA-targeted diagnostics and research.Entities:
Keywords: helicase-dependent isothermal amplification; nucleic acids; points-of-care diagnostics; polymerase chain reaction; primer dimer
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Year: 2015 PMID: 25953623 PMCID: PMC4489552 DOI: 10.1002/cbic.201500135
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164