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量化矿物-配体结构相似性:架起矿物地质世界与酶生物世界之间的桥梁。

Quantifying Mineral-Ligand Structural Similarities: Bridging the Geological World of Minerals with the Biological World of Enzymes.

作者信息

Zhao Daniel, Bartlett Stuart, Yung Yuk L

机构信息

Division of Geological and Planetary Sciences, California Institute of Technology, Pasadena, CA 91125, USA.

Department of Mathematics, Harvard University, Massachusetts Hall, Cambridge, MA 02138, USA.

出版信息

Life (Basel). 2020 Dec 10;10(12):338. doi: 10.3390/life10120338.

Abstract

Metal compounds abundant on Early Earth are thought to play an important role in the origins of life. Certain iron-sulfur minerals for example, are proposed to have served as primitive metalloenzyme cofactors due to their ability to catalyze organic synthesis processes and facilitate electron transfer reactions. An inherent difficulty with studying the catalytic potential of many metal compounds is the wide range of data and parameters to consider when searching for individual minerals and ligands of interest. Detecting mineral-ligand pairs that are structurally analogous enables more relevant selections of data to study, since structural affinity is a key indicator of comparable catalytic function. However, current structure-oriented approaches tend to be subjective and localized, and do not quantify observations or compare them with other potential targets. Here, we present a mathematical approach that compares structural similarities between various minerals and ligands using molecular similarity metrics. We use an iterative substructure search in the crystal lattice, paired with benchmark structural similarity methods. This structural comparison may be considered as a first stage in a more advanced analysis tool that will include a range of chemical and physical factors when computing mineral-ligand similarity. This approach will seek relationships between the mineral and enzyme worlds, with applications to the origins of life, ecology, catalysis, and astrobiology.

摘要

早期地球上丰富的金属化合物被认为在生命起源中发挥着重要作用。例如,某些铁硫矿物被认为曾作为原始金属酶辅因子,因为它们能够催化有机合成过程并促进电子转移反应。研究许多金属化合物的催化潜力存在一个固有困难,即在寻找感兴趣的单个矿物和配体时需要考虑大量的数据和参数。检测结构相似的矿物 - 配体对能够使研究数据的选择更具相关性,因为结构亲和力是可比催化功能的关键指标。然而,当前基于结构的方法往往具有主观性和局限性,并且没有对观察结果进行量化或与其他潜在目标进行比较。在此,我们提出一种数学方法,使用分子相似性度量来比较各种矿物和配体之间的结构相似性。我们在晶格中使用迭代子结构搜索,并结合基准结构相似性方法。这种结构比较可被视为更高级分析工具的第一阶段,该工具在计算矿物 - 配体相似性时将纳入一系列化学和物理因素。这种方法将探寻矿物世界与酶世界之间的关系,并应用于生命起源、生态学、催化和天体生物学领域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1894/7764262/9ec3a68bf2f5/life-10-00338-g001.jpg

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