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Systematic optimization and modification of a DNA aptamer with 2'-O-methyl RNA analogues.


ABSTRACT: Nucleic acid aptamers (NAAs) are short synthetic DNA or RNA molecules that specifically fold into distinct three-dimensional structures able to specifically recognize a target. While NAAs show unprecedented promise in a variety of applications, including sensing, therapeutics and diagnostics, one major limitation involves the lack of stability towards omnipresent nucleases. Therefore, we herein report a systematic truncation and incorporation of 2'-O-methyl bases to a DNA aptamer, which results in increased stability without affecting affinity. One of the newly designed analogues is stable up to 24 hours, demonstrating that 2'-O-methyl RNA is an attractive modification to DNA aptamers, especially when therapeutic applications are intended.

SUBMITTER: Maio G 

PROVIDER: S-EPMC5716488 | biostudies-literature | 2017 Mar

REPOSITORIES: biostudies-literature

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Systematic optimization and modification of a DNA aptamer with 2'-O-methyl RNA analogues.

Maio George G   Enweronye Osita O   Zumrut Hasan E HE   Batool Sana S   Van Nabeela N   Mallikaratchy Prabodhika P  

ChemistrySelect 20170306 7


Nucleic acid aptamers (NAAs) are short synthetic DNA or RNA molecules that specifically fold into distinct three-dimensional structures able to specifically recognize a target. While NAAs show unprecedented promise in a variety of applications, including sensing, therapeutics and diagnostics, one major limitation involves the lack of stability towards omnipresent nucleases. Therefore, we herein report a systematic truncation and incorporation of 2'-O-methyl bases to a DNA aptamer, which results  ...[more]

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