由DNA修饰酶驱动的合成分子开关
Hong Kang1,2, Yuexuan Yang1, Bryan Wei3
1School of Life Sciences, Center for Synthetic and Systems Biology, Tsinghua University, 100084, Beijing, China.
Nature communications
|May 6, 2024
概括
科学家们创造了由酶控制的合成DNA分子开关. 这些开关使得强大的,酶触发的DNA纳米结构的组装和拆卸,提供精确的控制复杂的分子架构.
科学领域:
- 生物化学 生物化学
- 合成生物学 合成生物学
- 纳米技术 纳米技术
背景情况:
- 自然生物系统广泛利用分子开关来进行生化调节.
- DNA纳米结构为构建复杂分子架构提供了多功能平台.
研究的目的:
- 设计和制造由DNA修饰酶激活的合成分子开关.
- 为了证明可控制的DNA纳米结构凝聚力和结构状态的ON/OFF切换.
主要方法:
- 利用DNA聚合酶和尼克内核酶进行酶控.
- 设计具有酶响应粘性末端凝聚力的合成DNA结构.
- 在极简的DNA系统,DNA网格和DNA原始化中实施开关机制.
主要成果:
- 证明了强大的,由酶触发的DNA纳米结构的组装和拆卸.
- 通过酶处理实现可控制的粘性端凝聚力的开启/关闭.
- 展示了复杂的DNA格子和原木系统中的形态变化.
结论:
- 酶驱动的DNA分子开关为控制DNA纳米结构组装和拆卸提供了强大的机制.
- 这种方法使复杂的分子架构能够在需要时精确地操纵.
- 开发的开关在合成生物学和纳米技术中具有潜在的应用.
相关概念视频
DNA-only Transposons
14.5K
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...
14.5K
DNA Topoisomerases
31.3K
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. ...
31.3K
Conservative Site-specific Recombination and Phase Variation
6.0K
Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
The recognition sites for Cre recombinase called LoxP...
The recognition sites for Cre recombinase called LoxP...
6.0K
Riboswitches
8.1K
Riboswitches are non-coding mRNA domains that regulate the transcription and translation of downstream genes without the help of proteins. Riboswitches bind directly to a metabolite and can form unique stem-loop or hairpin structures in response to the amount of the metabolite present. They have two distinct regions – a metabolite-binding aptamer and an expression platform.
The aptamer has high specificity for a particular metabolite which allows riboswitches to specifically regulate...
The aptamer has high specificity for a particular metabolite which allows riboswitches to specifically regulate...
8.1K
Single-Strand DNA Binding Proteins
14.1K
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...
14.1K
DNA Helicases
21.3K
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...
21.3K


