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阻抗匹配与遗传编码起源的替代途径选择。

Impedance Matching and the Choice Between Alternative Pathways for the Origin of Genetic Coding.

机构信息

Department of Physics and Te Ao Marama Centre for Fundamental Inquiry, University of Auckland, PB 92019, Auckland 1142, New Zealand.

Department of Biochemistry and Biophysics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-7260, USA.

出版信息

Int J Mol Sci. 2020 Oct 7;21(19):7392. doi: 10.3390/ijms21197392.

Abstract

We recently observed that errors in gene replication and translation could be seen qualitatively to behave analogously to the impedances in acoustical and electronic energy transducing systems. We develop here quantitative relationships necessary to confirm that analogy and to place it into the context of the minimization of dissipative losses of both chemical free energy and information. The formal developments include expressions for the information transferred from a template to a new polymer, I; an impedance parameter, Z; and an effective alphabet size, n; all of which have non-linear dependences on the fidelity parameter, q, and the alphabet size, n. Surfaces of these functions over the {n,q} plane reveal key new insights into the origin of coding. Our conclusion is that the emergence and evolutionary refinement of information transfer in biology follow principles previously identified to govern physical energy flows, strengthening analogies (i) between chemical self-organization and biological natural selection, and (ii) between the course of evolutionary trajectories and the most probable pathways for time-dependent transitions in physics. Matching the informational impedance of translation to the four-letter alphabet of genes uncovers a pivotal role for the redundancy of triplet codons in preserving as much intrinsic genetic information as possible, especially in early stages when the coding alphabet size was small.

摘要

我们最近观察到,基因复制和翻译中的错误可以定性地看作类似于声学和电子能量转换系统中的阻抗。我们在这里开发了必要的定量关系,以确认这种类比,并将其置于最小化化学自由能和信息的耗散损失的背景下。正式的发展包括从模板转移到新聚合物的信息 I 的表达式;阻抗参数 Z;和有效字母大小 n;所有这些都与保真度参数 q 和字母大小 n 具有非线性关系。这些函数在 {n,q} 平面上的表面揭示了编码起源的关键新见解。我们的结论是,生物学中信息传递的出现和进化细化遵循以前确定的物理能量流的原则,加强了化学自组织和生物自然选择之间的类比(i),以及进化轨迹的过程和物理中时变跃迁的最可能途径之间的类比(ii)。将翻译的信息阻抗与基因的四字母字母表匹配,揭示了三核苷酸密码子的冗余在尽可能多地保留内在遗传信息方面的关键作用,尤其是在编码字母表较小时的早期阶段。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4608/7582391/0efdcb9358fc/ijms-21-07392-g001.jpg

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