用单链DNA编程的纳米装置利用刺激流
Mulin Duan1, Yan Zhou1, Haoran Zheng1
1State Key Laboratory of Synergistic Chem-Bio Synthesis, School of Chemistry and Chemical Engineering, New Cornerstone Science Laboratory, Frontiers Science Center for Transformative Molecules and National Center for Translational Medicine, Shanghai Jiao Tong University, Shanghai, China.
Angewandte Chemie (International ed. in English)
|February 4, 2026
概括
研究人员开发了一种DNA纳米设备,用于高效的能量传输. 这一突破使用非对称的π-π相互作用和DNA空间限制来精确控制纳米设备.
科学领域:
- 纳米技术纳米技术
- 生物物理学的生物物理.
- 材料科学 材料科学 材料科学
背景情况:
- 纳米系统需要功能模块组件.
- 热力学不兼容性阻碍了精确的纳米设备集成.
研究的目的:
- 为了构建一个单链DNA (ssDNA) 导向的纳米设备,以实现高效的能量转导.
- 为了克服原子精确纳米设备集成的挑战.
主要方法:
- 利用ssDNA指导的自组装用于纳米设备的构造.
- 在DNA的空间限制中利用不对称的π-π相互作用来分裂激子能量水平.
- 设计了一个纳米设备,配有采光引擎,振动金属纳米集群执行器和可编程ssDNA.
主要成果:
- 通过受控刺激能级分裂,实现了94.3%的火效率.
- 证明了DNA的空间限制,为精确的排列策划了疏水性,共价性和π-π相互作用.
- 通过调整DNA长度和纳米集群连接体,通过调整DNA长度和纳米集群连接体,展示了对能量传输效率的持续控制.
结论:
- 建立了振动控制作为纳米级能量传导的一般范式.
- 开发了一个可编程平台,通过π-π相互作用操纵非辐射衰变.
- 能够实现精确的组件排列和在辐射和非辐射路径之间进行热驱动的切换.
相关概念视频
Single-Strand DNA Binding Proteins
16.7K
For successful DNA replication, the unwinding of double-stranded DNA must be accompanied by stabilization and protection of the separated single strands of the DNA. This crucial task is performed by single-strand DNA-binding (SSB) proteins. They bind to the DNA in a sequence-independent manner, which means that the nitrogenous bases of the DNA need not be present in a specific order for binding of SSB proteins to it. The binding of SSB proteins straightens single-stranded DNA (ssDNA) and makes...
16.7K
Lagging Strand Synthesis
61.4K
During replication, the complementary strands in double-stranded DNA are synthesized at different rates. Replication first begins on the leading strand. Replication starts later, occurs more slowly, and proceeds discontinuously on the lagging strand.
There are several major differences between synthesis of the leading strand and synthesis of the lagging strand. 1) Leading strand synthesis happens in the direction of replication fork opening, whereas lagging strand synthesis happens in the...
There are several major differences between synthesis of the leading strand and synthesis of the lagging strand. 1) Leading strand synthesis happens in the direction of replication fork opening, whereas lagging strand synthesis happens in the...
61.4K
Fixing Double-strand Breaks
14.8K
The double-stranded structure of DNA has two major advantages. First, it serves as a safe repository of genetic information where one strand serves as the back-up in case the other strand is damaged. Second, the double-helical structure can be wrapped around proteins called histones to form nucleosomes, which can then be tightly wound to form chromosomes. This way, DNA chains up to 2 inches long can be contained within microscopic structures in a cell. A double-stranded break not only damages...
14.8K
DNA Helicases
24.1K
DNA unwinding helicase enzymes are a type of motor protein. Motor proteins can translocate along filaments or polymers using energy generated from ATP hydrolysis. Helicases are involved in all the important cellular processes where DNA unwinding is required, such as DNA replication, repair, recombination, and transcription. They are present in all living organisms, but vary in their structure, function, and mechanism of action. For example, in prokaryotes, DnaB helicase binds and translocates...
24.1K
DNA Topoisomerases
35.6K
Topoisomerases are enzymes that relax overwound DNA molecules during various cell processes, including DNA replication and transcription. These enzymes regulate positive and negative DNA supercoiling without changing the nucleotide sequence. DNA overwinding in a clockwise direction results in positively supercoiled DNA, whereas underwinding in a counterclockwise direction produces negatively supercoiled DNA.
Types and Mechanism of action
Topoisomerases are divided into two main types. ...
Types and Mechanism of action
Topoisomerases are divided into two main types. ...
35.6K
DNA-only Transposons
17.5K
DNA-only transposons are called autonomous transposons since they code for the enzyme transposase that is required for the transposition mechanism. Insertion of transposons can alter gene functions in multiple ways. They can mutate the gene, alter gene expression by introducing a novel promoter or insulator sequence, introduce new splice sites, and change the mRNA transcripts produced, or remodel chromatin structure.
The donor site from where the transposon is excised is either degraded or...
The donor site from where the transposon is excised is either degraded or...
17.5K


