PNAs are emerging as useful synthetic devices targeting natural miRNAs. In particular 3 classes of structurally modified PNAs analogs are herein described, namely α, β and γ, which differ by their backbone modification. Their mode and binding affinity for natural nucleic acids and their use in medicinal chemistry as potential miRNA binders is discussed.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5329900PMC
http://dx.doi.org/10.1080/1949095X.2015.1107176DOI Listing

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