Low-cost genotyping method based on allele-specific recombinase polymerase amplification and colorimetric microarray detection

The costs of current genotyping methods limit their application to personalized therapy. The authors describe an alternative approach for the detection of single-point-polymorphisms using recombinant polymerase amplification as an allele-specific technique. The use of short and chemically modified p...

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Published inMikrochimica acta (1966) Vol. 184; no. 5; pp. 1453 - 1462
Main Authors Yamanaka, Eric Seiti, Tortajada-Genaro, Luis A., Maquieira, Ángel
Format Journal Article
LanguageEnglish
Published Vienna Springer Vienna 01.05.2017
Springer
Springer Nature B.V
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Abstract The costs of current genotyping methods limit their application to personalized therapy. The authors describe an alternative approach for the detection of single-point-polymorphisms using recombinant polymerase amplification as an allele-specific technique. The use of short and chemically modified primers and locked nucleic acids allowed for a selective isothermal amplification of wild-type or mutant variants at 37 °C within 40 min. An amplification chip platform containing 100 wells was manufactured with a 3D printer and using thermoplastic polylactic acid. The platform reduces reagent consumption and allows parallelization. As a proof of concept, the method was applied to the genotyping of four SNPs that are related to the treatment of tobacco addiction. The target polymorphisms included rs4680 (COMT gene), rs1799971 (OPRM1 gene), rs1800497 (ANKK1 gene), and rs16969968 (CHRNA5 gene). The genotype populations can be well discriminated. Graphical abstract Schematic of the allele-specific recombinase polymerase amplification for genotyping of polymorphisms. The isothermal discrimination reaction occurs in a multi-well amplification chip manufactured with a 3D printer and by using thermoplastic polylactic acid.
AbstractList The costs of current genotyping methods limit their application to personalized therapy. The authors describe an alternative approach for the detection of single-point-polymorphisms using recombinant polymerase amplification as an allele-specific technique. The use of short and chemically modified primers and locked nucleic acids allowed for a selective isothermal amplification of wild-type or mutant variants at 37 °C within 40 min. An amplification chip platform containing 100 wells was manufactured with a 3D printer and using thermoplastic polylactic acid. The platform reduces reagent consumption and allows parallelization. As a proof of concept, the method was applied to the genotyping of four SNPs that are related to the treatment of tobacco addiction. The target polymorphisms included rs4680 (COMT gene), rs1799971 (OPRM1 gene), rs1800497 (ANKK1 gene), and rs16969968 (CHRNA5 gene). The genotype populations can be well discriminated.
The costs of current genotyping methods limit their application to personalized therapy. The authors describe an alternative approach for the detection of single-point-polymorphisms using recombinant polymerase amplification as an allele-specific technique. The use of short and chemically modified primers and locked nucleic acids allowed for a selective isothermal amplification of wild-type or mutant variants at 37 °C within 40 min. An amplification chip platform containing 100 wells was manufactured with a 3D printer and using thermoplastic polylactic acid. The platform reduces reagent consumption and allows parallelization. As a proof of concept, the method was applied to the genotyping of four SNPs that are related to the treatment of tobacco addiction. The target polymorphisms included rs4680 (COMT gene), rs1799971 (OPRM1 gene), rs1800497 (ANKK1 gene), and rs16969968 (CHRNA5 gene). The genotype populations can be well discriminated. Graphical abstract Schematic of the allele-specific recombinase polymerase amplification for genotyping of polymorphisms. The isothermal discrimination reaction occurs in a multi-well amplification chip manufactured with a 3D printer and by using thermoplastic polylactic acid.
Audience Academic
Author Maquieira, Ángel
Tortajada-Genaro, Luis A.
Yamanaka, Eric Seiti
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  surname: Yamanaka
  fullname: Yamanaka, Eric Seiti
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  givenname: Luis A.
  surname: Tortajada-Genaro
  fullname: Tortajada-Genaro, Luis A.
  organization: Instituto Inter-universitario de Reconocimiento Molecular y Desarrollo Tecnológico (IDM) - Departamento de Química, Universitat Politècnica de València, Unidad Mixta UPV-La Fe, Nanomedicine and Sensors, Instituto de Investigacion Sanitaria La Fe
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  fullname: Maquieira, Ángel
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  organization: Instituto Inter-universitario de Reconocimiento Molecular y Desarrollo Tecnológico (IDM) - Departamento de Química, Universitat Politècnica de València, Unidad Mixta UPV-La Fe, Nanomedicine and Sensors, Instituto de Investigacion Sanitaria La Fe
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Issue 5
Keywords Isothermal amplification
gene
Tobacco addiction
3D–printer
ANKK1 gene
Micro-well plate
Microchip
SNP genotyping
Pharmacogenomics
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Snippet The costs of current genotyping methods limit their application to personalized therapy. The authors describe an alternative approach for the detection of...
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SubjectTerms Amplification
Analysis
Analytical Chemistry
Characterization and Evaluation of Materials
Chemical reduction
Chemistry
Chemistry and Materials Science
Colorimetry
Economic aspects
Genetic aspects
Genetic polymorphisms
Methods
Microengineering
Nanochemistry
Nanotechnology
Nucleic acids
Original Paper
Polylactic acid
Populations
Reagents
Thermoplastics
Three dimensional printing
Tobacco
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Title Low-cost genotyping method based on allele-specific recombinase polymerase amplification and colorimetric microarray detection
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