首页> 外文期刊>Computational and Structural Biotechnology Journal >{OPEN} {QUESTIONS} {IN} {ORIGIN} {OF} LIFE: {EXPERIMENTAL} {STUDIES} {ON} {THE} {ORIGIN} {OF} {NUCLEIC} {ACIDS} {AND} {PROTEINS} {WITH} {SPECIFIC} {AND} {FUNCTIONAL} {SEQUENCES} {BY} A {CHEMICAL} {SYNTHETIC} {BIOLOGY} {APPROACH}
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{OPEN} {QUESTIONS} {IN} {ORIGIN} {OF} LIFE: {EXPERIMENTAL} {STUDIES} {ON} {THE} {ORIGIN} {OF} {NUCLEIC} {ACIDS} {AND} {PROTEINS} {WITH} {SPECIFIC} {AND} {FUNCTIONAL} {SEQUENCES} {BY} A {CHEMICAL} {SYNTHETIC} {BIOLOGY} {APPROACH}

机译:{OPEN} {QUESTIONS} {IN} {ORIGIN} {OF}寿命:{EXPERIMENTAL} {STUDIES} {ON} {THE} {ORIGIN} {OF} {NUCLEIC} {ACIDS} {AND} {PROTINS} {特定} {和} {功能} {序列} {BY} {化学} {合成} {生物学} {方法}

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In this mini-review we present some experimental approaches to the important issue in the origin of life, namely the origin of nucleic acids and proteins with specific and functional sequences. The formation of macromolecules on prebiotic Earth faces practical and conceptual difficulties. From the chemical viewpoint, macromolecules are formed by chemical pathways leading to the condensation of building blocks (amino acids, or nucleotides) in long-chain copolymers (proteins and nucleic acids, respectively). The second difficulty deals with a conceptual problem, namely with the emergence of specific sequences among a vast array of possible ones, the huge “sequence space”, leading to the question “why these macromolecules, and not the others?” We have recently addressed these questions by using a chemical synthetic biology approach. In particular, we have tested the catalytic activity of small peptides, like Ser-His, with respect to peptide- and nucleotides-condensation, as a realistic model of primitive organocatalysis. We have also set up a strategy for exploring the sequence space of random proteins and {RNAs} (the so-called “never born biopolymer” project) with respect to the production of folded structures. Being still far from solved, the main aspects of these “open questions” are discussed here, by commenting on recent results obtained in our groups and by providing a unifying view on the problem and possible solutions. In particular, we propose a general scenario for macromolecule formation via fragment-condensation, as a scheme for the emergence of specific sequences based on molecular growth and selection.
机译:在这份小型回顾中,我们介绍了一些解决生命起源中重要问题的实验方法,即具有特定功能序列的核酸和蛋白质的起源。在益生元地球上形成大分子面临实际和概念上的困难。从化学观点来看,大分子是通过化学途径形成的,导致长链共聚物(分别为蛋白质和核酸)中的结构单元(氨基酸或核苷酸)缩合。第二个难题涉及一个概念性问题,即在众多可能的序列中出现了特定的序列,巨大的“序列空间”,从而引发了一个问题:“为什么这些大分子而不是其他大分子?”我们最近通过使用化学合成生物学方法解决了这些问题。尤其是,我们已经测试了小肽(如Ser-His)对肽和核苷酸缩合的催化活性,作为原始有机催化的现实模型。我们还制定了一种策略,用于探索折叠结构产生方面的随机蛋白质和{RNAs}(所谓的“永生生物聚合物”项目)的序列空间。这些“悬而未决的问题”的主要方面仍然遥遥无期,在本文中将对我们小组最近取得的成果进行评论,并就问题和可能的解决方案提供统一的观点,以进行讨论。特别是,我们提出了一种通过片段缩合形成大分子的一般方案,作为基于分子生长和选择的特定序列出现的方案。

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