Rolling Circle Amplification with Chemically Modified Nucleoside Triphosphates
Abstract
Modified nucleoside triphosphates (dN*TPs) represent facile and versatile precursors
for the introduction of chemical diversity into nucleic acids. While
dN*TPs have been utilized in a plethora of practical applications, very little
attention has been devoted to the assessment of their compatibility with isothermal
amplification strategies. In this context, rolling circle amplification (RCA)
is a wide-spread enzymatic replication method in which small single-stranded
DNA (ssDNA) circles serve as templates in primer extension reactions yielding
very long, ssDNA products. RCA is a pivotal tool for the generation of biosensor
and diagnostic devices and is currently evaluated for its usefulness to create
novel drug delivery systems. This unit describes the experimental procedures
for the synthesis of modified RCA products using dN*TPs bearing chemical
alterations at any possible location of the nucleosidic scaffold. Two ligation
methods are presented for the generation of the DNA nanocircles that serve as
templates for RCA, followed by a description of the RCA method itself and an
assessment of the nuclease resistance of the ensuing products.
Domains
Chemical Sciences
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