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. 2018 Jan 24;46(4):1614–1623. doi: 10.1093/nar/gky024

Figure 2.

Figure 2.

(A) Structures of chemically modified nucleotides incorporated in ps- and aps-duplexes. (B) Sequence of the synthesized dodecamers for parallel and antiparallel strand pairings. Underlined residues (N) contain the isonucleobase modifications. Check marks indicate duplexes with significant melting transitions; open circles refer to combinations that did not yield a melting transition (see Table 1). “-" means “not measured".