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具有生物相关功能基团的铍配合物:配位几何和结合亲和力。

Beryllium Complexes with Bio-Relevant Functional Groups: Coordination Geometries and Binding Affinities.

机构信息

Anorganische Chemie, Nachwuchsgruppe Berylliumchemie, Fachbereich Chemie, Philipps-Universität Marburg, Hans-Meerwein-Strasse 4, 35032, Marburg, Germany.

出版信息

Angew Chem Int Ed Engl. 2018 Jul 16;57(29):9180-9184. doi: 10.1002/anie.201803667. Epub 2018 May 16.

Abstract

The coordination mode around beryllium in proteins and the binding affinity towards the peptide are unknown because there have been no coordination compounds of beryllium with ligands bearing bio-relevant functional groups. We report the first comprehensive study on Be complexes with monodentate carboxylic acids, esters, aldehydes, and alcohols. Through solution and solid-state techniques we determined that the binding affinities of Be ions towards the functional groups are: carboxylate > alcohol > aldehyde > ester. Crystal structures of all the compounds have been determined including the unprecedented dodeca-nuclear macrocyclic ring structure of non-basic beryllium benzoate, which is the first example of those beryllium carboxylates. These findings enable the evaluation of potential beryllium binding sites inside proteins and is required to understand the mechanism of metal-triggered immune responses.

摘要

由于没有含生物相关官能团的配体的铍配位化合物,因此,蛋白质中铍的配位模式以及与肽的结合亲和力尚不清楚。我们报告了首例关于具有单齿羧酸、酯、醛和醇配体的铍配合物的综合研究。通过溶液和固态技术,我们确定了 Be 离子与官能团的结合亲和力为:羧酸盐>醇>醛>酯。所有化合物的晶体结构都已确定,包括前所未有的非碱性苯甲酸铍十二核大环结构,这是此类铍羧酸盐的首例。这些发现使我们能够评估蛋白质内部潜在的铍结合位点,并有助于理解金属引发免疫反应的机制。

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