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Covalent Linkage of One-Dimensional DNA Arrays Bonded by Paranemic Cohesion

机译:一维DNA阵列通过旁神经凝聚力的共价键。

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The construction of DNA nanostructures from branched DNA motifs, or tiles, typically relies on the use of sticky-ended cohesion, owing to the specificity and programmability of DNA sequences. The stability of such constructs when unligated is restricted to a specific range of temperatures, owing to the disruption of base pairing at elevated temperatures. Paranemic (PX) cohesion was developed as an alternative to sticky ends for the cohesion of large topologically closed species that could be purified reliably on denaturing gels. However, PX cohesion is also of limited stability. In this work, we added sticky-ended interactions to PX-cohesive complexes to create interlocked complexes by functionalizing the sticky ends with psoralen, which can form cross-links between the two strands of a double helix. We were able to reinforce the stability of the constructs by creating covalent linkages between the 3'-ends and 5'-ends of the sticky ends; the sticky ends were added to double crossover domains via 3'-3' and 5'-5' linkages. Catenated arrays were obtained either by enzymatic ligation or by UV cross-linking. We have constructed finite-length one-dimensional arrays linked by interlocking loops and have positioned streptavidin gold particles on these constructs.
机译:由于DNA序列的特异性和可编程性,由分支的DNA基序或瓦片构建DNA纳米结构通常依赖于粘性末端内聚。由于在高温下碱基配对的破坏,这种构建物在未连接时的稳定性被限制在特定的温度范围内。开发了Paranemic(PX)内聚力,作为粘性末端的替代方法,用于粘附在拓扑上封闭的大型物种,这些物种可以在变性凝胶上可靠地纯化。但是,PX内聚的稳定性也有限。在这项工作中,我们将粘性末端的相互作用添加到PX粘性复合物中,通过使用补骨脂素官能化粘性末端来创建互锁的复合物,补骨脂素可以在双螺旋的两条链之间形成交联。通过在粘性末端的3'末端和5'末端之间建立共价键,我们能够增强构建体的稳定性;粘性末端通过3'-3'和5'-5'连接添加到双交换域。通过酶促连接或通过UV交联获得链状阵列。我们构建了由互锁环链接的有限长一维阵列,并将链霉亲和素金颗粒定位在这些构建体上。

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