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一种光释放的潜在前体核苷酸激活剂。

A Light-Releasable Potentially Prebiotic Nucleotide Activating Agent.

机构信息

MRC Laboratory of Molecular Biology , Francis Crick Avenue , Cambridge Biomedical Campus, Cambridge CB2 0QH , U.K.

出版信息

J Am Chem Soc. 2018 Jul 18;140(28):8657-8661. doi: 10.1021/jacs.8b05189. Epub 2018 Jul 3.

Abstract

Investigations into the chemical origin of life have recently benefitted from a holistic approach in which possible atmospheric, organic, and inorganic systems chemistries are taken into consideration. In this way, we now report that a selective phosphate activating agent, namely methyl isocyanide, could plausibly have been produced from simple prebiotic feedstocks. We show that methyl isocyanide drives the conversion of nucleoside monophosphates to phosphorimidazolides under potentially prebiotic conditions and in excellent yields for the first time. Importantly, this chemistry allows for repeated reactivation cycles, a property long sought in nonenzymatic oligomerization studies. Further, as the isocyanide is released upon irradiation, the possibility of spatially and temporally controlled activation chemistry is thus raised.

摘要

近年来,对生命化学起源的研究得益于一种整体方法,其中考虑了可能的大气、有机和无机系统化学。通过这种方式,我们现在报告说,一种选择性的磷酸激活剂,即甲基异氰酸酯,可能是由简单的前体生物原料产生的。我们首次表明,甲基异氰酸酯可以在潜在的前生物条件下驱动核苷单磷酸转化为磷酰亚咪唑盐,并且产率非常高。重要的是,这种化学允许重复的再激活循环,这是在非酶聚合研究中长期寻求的性质。此外,由于异氰化物在辐照时释放,因此有可能实现空间和时间控制的激活化学。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/187e/6152610/47864a896423/ja-2018-05189n_0001.jpg

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