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Hinge-initiated Primer-dependent Amplification of Nucleic Acids (HIP) – A New Versatile Isothermal Amplification Method
by
Fischbach, Jens
, Frohme, Marcus
, Glökler, Jörn
in
45/77
/ 631/326/421
/ 631/337/151/1431
/ Binding sites
/ Copy number
/ Displacement activity
/ DNA Primers
/ Gene Dosage
/ Hip
/ Humanities and Social Sciences
/ multidisciplinary
/ Nucleic Acid Amplification Techniques
/ Nucleic Acids
/ Science
/ Science (multidisciplinary)
2017
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Hinge-initiated Primer-dependent Amplification of Nucleic Acids (HIP) – A New Versatile Isothermal Amplification Method
by
Fischbach, Jens
, Frohme, Marcus
, Glökler, Jörn
in
45/77
/ 631/326/421
/ 631/337/151/1431
/ Binding sites
/ Copy number
/ Displacement activity
/ DNA Primers
/ Gene Dosage
/ Hip
/ Humanities and Social Sciences
/ multidisciplinary
/ Nucleic Acid Amplification Techniques
/ Nucleic Acids
/ Science
/ Science (multidisciplinary)
2017
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While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Hinge-initiated Primer-dependent Amplification of Nucleic Acids (HIP) – A New Versatile Isothermal Amplification Method
by
Fischbach, Jens
, Frohme, Marcus
, Glökler, Jörn
in
45/77
/ 631/326/421
/ 631/337/151/1431
/ Binding sites
/ Copy number
/ Displacement activity
/ DNA Primers
/ Gene Dosage
/ Hip
/ Humanities and Social Sciences
/ multidisciplinary
/ Nucleic Acid Amplification Techniques
/ Nucleic Acids
/ Science
/ Science (multidisciplinary)
2017
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Hinge-initiated Primer-dependent Amplification of Nucleic Acids (HIP) – A New Versatile Isothermal Amplification Method
Journal Article
Hinge-initiated Primer-dependent Amplification of Nucleic Acids (HIP) – A New Versatile Isothermal Amplification Method
2017
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Overview
The growing demand for cost-effective nucleic acid detection assays leads to an increasing number of different isothermal amplification reaction methods. However, all of the most efficient methods suffer from highly complex assay conditions due to the use of complicated primer sets and/or auxiliary enzymes. The present study describes the application of a new linker moiety that can be incorporated between a primer and a secondary target binding site which can act both as a block to polymerase extension as well as a hinge for refolding. This novel “hinge-primer” approach results in an efficient regeneration of the primer binding site and thus improves the strand-displacement and amplification process under isothermal conditions. Our investigations revealed that the reaction with forward and reverse hinge-primer including an abasic site is very efficient. The assay complexity can be reduced by combining the hinge-primer with a corresponding linear primer. Furthermore, the reaction speed can be increased by reducing the length of the amplified target sequence. We tested the sensitivity down to 10
4
copies and found a linear correlation between reaction time and input copy number. Our approach overcomes the usually cumbersome primer-design and extends the range of isothermal amplification methods using a polymerase with strand-displacement activity.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
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