Vecchioni Simon, Lu Brandon, Livernois William, Ohayon Yoel P, Yoder Jesse B, Yang Chu-Fan, Woloszyn Karol, Bernfeld William, Anantram M P, Canary James W, Hendrickson Wayne A, Rothschild Lynn J, Mao Chengde, Wind Shalom J, Seeman Nadrian C, Sha Ruojie
Department of Chemistry, New York University, New York, NY, 10003, USA.
Department of Electrical and Computer Engineering, University of Washington, Seattle, WA, 98195, USA.
Adv Mater. 2023 Mar 20:e2201938. doi: 10.1002/adma.202201938.
DNA double helices containing metal-mediated DNA (mmDNA) base pairs have been constructed from Ag and Hg ions between pyrimidine:pyrimidine pairs with the promise of nanoelectronics. Rational design of mmDNA nanomaterials has been impractical without a complete lexical and structural description. Here, we explore the programmability of structural DNA nanotechnology toward its founding mission of self-assembling a diffraction platform for biomolecular structure determination. We employed the tensegrity triangle to build a comprehensive structural library of mmDNA pairs via X-ray diffraction and elucidated generalized design rules for mmDNA construction. We uncovered two binding modes: N3-dominant, centrosymmetric pairs and major groove binders driven by 5-position ring modifications. Energy gap calculations showed additional levels in the lowest unoccupied molecular orbitals (LUMO) of mmDNA structures, rendering them attractive molecular electronic candidates. This article is protected by copyright. All rights reserved.
含有金属介导的DNA(mmDNA)碱基对的DNA双螺旋已通过嘧啶与嘧啶对之间的银离子和汞离子构建而成,有望应用于纳米电子学。如果没有完整的词汇和结构描述,mmDNA纳米材料的合理设计是不切实际的。在这里,我们探索结构DNA纳米技术的可编程性,以实现其构建用于生物分子结构测定的衍射平台的初始使命。我们利用张拉整体三角形通过X射线衍射构建了mmDNA对的综合结构库,并阐明了mmDNA构建的通用设计规则。我们发现了两种结合模式:以N3为主的中心对称对和由5位环修饰驱动的大沟结合剂。能隙计算表明,mmDNA结构的最低未占据分子轨道(LUMO)中有额外的能级,使其成为有吸引力的分子电子学候选物。本文受版权保护。保留所有权利。