Locked nucleoside analogues expand the potential of DNAzymes to cleave structured RNA targets.

ABSTRACT:

Background

DNAzymes cleave at predetermined sequences within RNA. A prerequisite for cleavage is that the DNAzyme can gain access to its target, and thus the DNAzyme must be capable of unfolding higher-order structures that are present in the RNA substrate. However, in many cases the RNA target sequence is hidden in a region that is too tightly structured to be accessed under physiological conditions by DNAzymes.

Results

We investigated how incorporation of LNA (locked nucleic acid) monomers into DNAzymes improves their ability to gain access and cleave at highly-structured RNA targets. The binding arms of DNAzymes were varied in length and were substituted with up to three LNA and alpha-L-LNA monomers (forming LNAzymes). For one DNAzyme, the overall cleavage reaction procee

SUBMITTER: Vester B 

PROVIDER: S-EPMC1501032 | biostudies-literature | 2006 Jun

REPOSITORIES: biostudies-literature