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DNA Scaffold Nanostructures for Efficient and Directional Propagation of Light Harvesting Cascades

机译:DNA支架纳米结构的光收集叶栅的有效和定向传播。

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摘要

The development of light harvesting systems for directed, efficient control of energy transfer at the biomolecular level has generated considerable interest in the past decade. Molecular fluorophores provide a straightforward mechanism for determining nanoscale distance changes through Forster resonance energy transfer (FRET), and many systems seek to build off of this simple yet powerful principle to provide additional functionality. The use of DNA-based integrated biomolecular devices offer many unique advantages towards this end. DNA itself is an excellent engineering material - it is innately biocompatible, quickly and cheaply synthesized, and complex structures can be readily designed in silico. It also provides an excellent scaffold for the precise patterning of various biomolecules. Here, we discuss the systems that have been recently developed which add to this toolbox, including nanostructural dye patterning, photonic wires, and the incorporation of alternative energy propagation modalities, such as semiconductor quantum dots (QD) and the bioluminescent protein luciferase. In particular, we explore the incorporation of luciferase into various nanostructural conformations, providing the capability to efficiently control energy flow directionality. We discuss the nature of this system, including unexpected spectral complexities, in the context of the field.
机译:在过去的十年中,用于在生物分子水平上直接,有效地控制能量转移的光收集系统的发展引起了人们的极大兴趣。分子荧光团为通过Forster共振能量转移(FRET)确定纳米级距离变化提供了一种简单的机制,许多系统都在此简单而强大的原理的基础上提供更多功能。为此,基于DNA的集成生物分子设备的使用提供了许多独特的优势。 DNA本身是一种出色的工程材料-它天生具有生物相容性,可以快速廉价地合成,并且可以通过计算机轻松设计复杂的结构。它还为各种生物分子的精确构图提供了出色的支架。在这里,我们讨论了最近开发的系统,这些系统已添加到该工具箱中,包括纳米结构染料图案,光子线以及替代性能量传播方式的合并,例如半导体量子点(QD)和生物发光蛋白荧光素酶。特别是,我们探索将萤光素酶整合到各种纳米结构构象中,从而提供有效控制能量流方向性的能力。在现场的背景下,我们讨论了该系统的性质,包括意想不到的光谱复杂性。

著录项

  • 来源
  • 会议地点 San Diego(US)
  • 作者单位

    Center for Bio/Molecular Science and Engineering, Code 6900, U.S. Naval Research Laboratory, Washington, D.C. 20375 U.S.A.,College of Science, George Mason University, Fairfax, VA 22030, U.S.A.;

    Center for Bio/Molecular Science and Engineering, Code 6900, U.S. Naval Research Laboratory, Washington, D.C. 20375 U.S.A.;

    Center for Bio/Molecular Science and Engineering, Code 6900, U.S. Naval Research Laboratory, Washington, D.C. 20375 U.S.A.;

    Center for Bio/Molecular Science and Engineering, Code 6900, U.S. Naval Research Laboratory, Washington, D.C. 20375 U.S.A.;

    Center for Bio/Molecular Science and Engineering, Code 6900, U.S. Naval Research Laboratory, Washington, D.C. 20375 U.S.A.;

    Center for Bio/Molecular Science and Engineering, Code 6900, U.S. Naval Research Laboratory, Washington, D.C. 20375 U.S.A.;

    Center for Bio/Molecular Science and Engineering, Code 6900, U.S. Naval Research Laboratory, Washington, D.C. 20375 U.S.A.;

  • 会议组织
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Luciferase; DNA nanoscaffold; FRET; BRET; light harvesting; dendrimer; bionanotechnology; biophotonics;

    机译:萤光素酶DNA纳米支架烦恼;布雷特采光树枝状聚合物生物技术生物光子学;
  • 入库时间 2022-08-26 13:44:26

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