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首页> 外文期刊>Journal of the American Chemical Society >Designed α-helical Tectons For Constructing Multicomponent Syntheticbiological Systems
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Designed α-helical Tectons For Constructing Multicomponent Syntheticbiological Systems

机译:设计用于构建多组分合成生物学系统的α-螺旋结构

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One route to develop new synthetic-biological systems is to assemble discrete nanoscale objects from programmed peptide-based building blocks, or tectons. This would require tectons that exhibit high fidelity interactions with specified partners, and the potential to be functionalized. Such a set of peptidic building blocks could be used to create more-complex assemblies analogous to the way that DNA has been used design a wide range of 2D and 3D nanostructures. While DNA-based assemblies have reached the level of sophistication to allow control of structure and even motion, the use of peptidic building blocks is far less advanced. This is because the rules relating peptide sequence to structure are less well established than the exquisite specificity of base pairing in DNA. Although the design of peptidic tectons is more difficult, the potential benefits include ease of production, functionalization, and versatility. Here we present an algorithm to search coiled-coil specificity space, along with a few modest multicomponent structures to demonstrate our ability to build peptide-based nano-structures from the bottom up.
机译:开发新的合成生物学系统的一种方法是,从基于程序化的基于肽的构造块或构造物组装离散的纳米级物体。这将需要与特定伙伴表现出高保真度交互作用的构造,并具有被功能化的潜力。这样的一组肽构建基块可用于创建更复杂的装配体,类似于使用DNA设计多种2D和3D纳米结构的方式。虽然基于DNA的装配体已经达到了可以控制结构甚至运动的复杂程度,但是肽类构建模块的使用却远远落后。这是因为,与DNA中碱基配对的精确特异性相比,将肽序列与结构相关的规则建立得不够好。尽管肽构造的设计较为困难,但潜在的好处包括易于生产,功能化和多功能性。在这里,我们提出一种搜索卷曲螺旋特异性空间的算法,以及一些适度的多组分结构,以证明我们自下而上构建基于肽的纳米结构的能力。

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