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. 2019 Sep 25;9:13856. doi: 10.1038/s41598-019-49862-y

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© The Author(s) 2019

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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LiNAs for liposome fusion. (A) Schematic of liposome docking via hybridization of LiNA strands. The inset shows anchor structure and connectivity (drawing not to scale). (B) LiNA sequences with or without triethylene glycol phosphate spacer unit (P3). Duplexes between LiNAs complementary reference DNAs, i.e. the 17-nt zipper-sequence alone, have a T_m of around 57 ± 1 °C (see Supplementary information, Table S2).