4.8 Article

Long-Range Ordering of Blunt-Ended DNA Tiles on Supported Lipid Bilayers

期刊

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 139, 期 34, 页码 12027-12034

出版社

AMER CHEMICAL SOC
DOI: 10.1021/jacs.7b06572

关键词

-

资金

  1. NSERC
  2. CIHR
  3. CFI
  4. Canada Research Chairs Program
  5. FRQNT
  6. CSACS

向作者/读者索取更多资源

Long-range ordering of DNA crossover tiles with blunt ends on lipid bilayers is investigated using atomic force microscopy. Blunt-ended tiles do not have single-stranded complementary ends, and thus instead of assembling via base pairing, they can interact by pi-stacking of their duplex ends. This work demonstrates that the balance of base pi-stacking interactions between the ends of DNA duplexes, cholesterol mediated DNA anchoring, and electrostatic DNA binding to supported lipid bilayers (SLBs) presents an opportunity to build dynamic materials with long-range order on a soft support. The tiles are shown to organize into novel tunable surface packing morphologies on the micrometer scale. This work focuses on three-point star (3PS) tiles that are either unmodified or modified with a cholesterol unit and investigates their interactions on supported lipid bilayers. On fluid bilayers, the cholesterol tiles form extended hexagonal arrays with few defects, while the unmodified tiles do not bind. In contrast, both modified and unmodified tiles bind to gel-phase bilayers and produce arrays of new organized morphologies. With increasing tile concentration, we observe a range of motifs, that progressively favor tile-tile packing over duplex-end pi-stacking. These structures can selectively pattern domains of phase-separated lipid bilayers, and the patterning is also observed for four-arm cross tiles. Dynamic blunt end contacts promote error correction and network reconfiguration to maximize favorable interactions with the substrate and are required for the observed tile organization. These results suggest that small blunt-ended tiles can be used as a platform to organize oligonucleotides, nanoparticles, and proteins into extensive networks at the interface with biologically relevant membrane systems or other soft surface materials for applications in cellular recognition, plasmonics, light harvesting, model systems for membrane protein assemblies, or analytical devices.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据