دورية أكاديمية

Visual Detection of Stem-Loop Primer Amplification (SPA) Products without Denaturation Using Peroxidase-like DNA Machines (PxDM).

التفاصيل البيبلوغرافية
العنوان: Visual Detection of Stem-Loop Primer Amplification (SPA) Products without Denaturation Using Peroxidase-like DNA Machines (PxDM).
المؤلفون: Maltzeva YI; Laboratory of Solution Chemistry of Advanced Materials and Technologies, ITMO University, 191002 St. Petersburg, Russia., Gorbenko DA; Laboratory of Solution Chemistry of Advanced Materials and Technologies, ITMO University, 191002 St. Petersburg, Russia., Nikitina EV; Pediatric Research and Clinical Center for Infectious Diseases, 197022 St. Petersburg, Russia., Rubel MS; Laboratory of Solution Chemistry of Advanced Materials and Technologies, ITMO University, 191002 St. Petersburg, Russia., Kolpashchikov DM; Chemistry Department, University of Central Florida, 4000 Central Florida Boulevard, Orlando, FL 32816, USA.; Burnett School of Biomedical Sciences, University of Central Florida, Orlando, FL 32816, USA.; National Center for Forensic Science, University of Central Florida, Orlando, FL 32826, USA.
المصدر: International journal of molecular sciences [Int J Mol Sci] 2023 Apr 25; Vol. 24 (9). Date of Electronic Publication: 2023 Apr 25.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: MDPI Country of Publication: Switzerland NLM ID: 101092791 Publication Model: Electronic Cited Medium: Internet ISSN: 1422-0067 (Electronic) Linking ISSN: 14220067 NLM ISO Abbreviation: Int J Mol Sci Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Basel, Switzerland : MDPI, [2000-
مواضيع طبية MeSH: Peroxidase* , Nucleic Acids*, DNA ; Nucleic Acid Amplification Techniques/methods ; Polymerase Chain Reaction/methods ; Peroxidases ; Sensitivity and Specificity
مستخلص: Rapid, inexpensive, and accurate determination of nucleic acids is a decisive factor in evaluating population's health and monitoring treatment at point-of-care (POC) settings. Testing systems with visual outputs can provide instrument-free signal detection. Isothermal amplification technologies can substitute conventional polymerase chain reaction (PCR) testing due to compatibility with the POC diagnostic. Here, we have visually detected DNA fragments obtained by stem-loop-primer-assisted isothermal amplification (SPA), but not those obtained by PCR or LAMP amplification using DNA nanomachines with peroxidase-like activity (PxDM) with sensitivity to a single nucleotide substitution. Compared to the diagnostics with conventional loop-mediated isothermal amplification (LAMP), the PxDM method produces no false positive signals with the non-specific amplification products. The study suggests that PxDM, in conjunction with SPA isothermal amplification, can become a valid platform for POC testing systems.
References: Bioinformatics. 2012 Apr 15;28(8):1166-7. (PMID: 22368248)
Clin Microbiol Infect. 2011 Feb;17(2):285-91. (PMID: 20156216)
Nucleic Acids Res. 2003 Jul 1;31(13):3406-15. (PMID: 12824337)
Sci Rep. 2016 Apr 01;6:23949. (PMID: 27032385)
Chem Commun (Camb). 2022 Apr 28;58(35):5395-5398. (PMID: 35415727)
Analyst. 2019 Jan 21;144(2):416-420. (PMID: 30600819)
Mol Biosyst. 2010 May;6(5):792-4. (PMID: 20567764)
Anal Chem. 2018 Jun 5;90(11):6580-6586. (PMID: 29667809)
Chembiochem. 2013 Nov 4;14(16):2087-90. (PMID: 24106198)
J Microbiol Methods. 2021 Aug;187:106199. (PMID: 33771524)
Chem Commun (Camb). 2016 Dec 6;52(99):14318-14321. (PMID: 27886299)
J Comput Chem. 2011 Jan 15;32(1):170-3. (PMID: 20645303)
Clin Chim Acta. 2019 Jun;493:138-147. (PMID: 30853460)
J Infect Chemother. 2013 Jun;19(3):404-11. (PMID: 23539453)
Nucleic Acids Res. 2005 Jul 1;33(Web Server issue):W577-81. (PMID: 15980540)
J Clin Microbiol. 2012 Nov;50(11):3443-50. (PMID: 22875898)
PLoS One. 2012;7(8):e43862. (PMID: 22952791)
ACS Phys Chem Au. 2021 Nov 24;1(1):45-53. (PMID: 34939072)
J Clin Lab Anal. 2021 Jan;35(1):e23643. (PMID: 33107116)
Clin Chem. 2007 Nov;53(11):2020-3. (PMID: 18030700)
Biosens Bioelectron. 2018 Apr 15;102:179-188. (PMID: 29136589)
J Clin Microbiol. 2009 Sep;47(9):2812-7. (PMID: 19571025)
Chem Biol. 1998 Sep;5(9):505-17. (PMID: 9751647)
Biosens Bioelectron. 2021 Jul 15;184:113239. (PMID: 33857727)
Molecules. 2015 Apr 07;20(4):6048-59. (PMID: 25853320)
BMC Biotechnol. 2006 Jan 10;6:3. (PMID: 16401354)
Anal Chem. 2019 Jun 4;91(11):6991-6995. (PMID: 31099243)
Nat Protoc. 2008;3(5):877-82. (PMID: 18451795)
Anal Chim Acta. 2016 Nov 2;943:114-122. (PMID: 27769370)
Angew Chem Int Ed Engl. 2019 Mar 26;58(14):4654-4658. (PMID: 30693619)
J Infect Chemother. 2009 Apr;15(2):62-9. (PMID: 19396514)
Anal Bioanal Chem. 2019 Feb;411(6):1211-1218. (PMID: 30617407)
Biomol Detect Quantif. 2015 Dec 30;7:1-8. (PMID: 27077046)
Chem Commun (Camb). 2010 May 21;46(19):3250-2. (PMID: 20442880)
معلومات مُعتمدة: 22-75-10073 Russian Science Foundation
فهرسة مساهمة: Keywords: DNA-nanomachine; G-quadruplex; detection of dsDNA amplicons; isothermal amplification; point-of-care diagnostics; single nucleotide selectivity
المشرفين على المادة: EC 1.11.1.7 (Peroxidase)
9007-49-2 (DNA)
0 (Nucleic Acids)
EC 1.11.1.- (Peroxidases)
تواريخ الأحداث: Date Created: 20230513 Date Completed: 20230515 Latest Revision: 20231102
رمز التحديث: 20240628
مُعرف محوري في PubMed: PMC10177805
DOI: 10.3390/ijms24097812
PMID: 37175522
قاعدة البيانات: MEDLINE
الوصف
تدمد:1422-0067
DOI:10.3390/ijms24097812