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2-苯甲酰吡啶配体与金的络合对基于炔丙基酯的蛋白质标记至关重要。

2-Benzoylpyridine Ligand Complexation with Gold Critical for Propargyl Ester-Based Protein Labeling.

机构信息

Biofunctional Synthetic Chemistry Laboratory, RIKEN Cluster for Pioneering Research, 2-1 Hirosawa, Wako-shi, Saitama, 351-0198, Japan.

Division of Material Science, Graduate School of Science and Engineering, Saitama University, 255 Shimo-Okubo, Sakura-ku, Saitama, 338-8570, Japan.

出版信息

Chemistry. 2018 Jul 25;24(42):10595-10600. doi: 10.1002/chem.201802058. Epub 2018 Jul 16.

Abstract

In previously reported work, Au complexes coordinated with 2-benzoylpyridine ligand, BPy-Au, were prebound to a protein and used to discover a novel protein-directed labeling approach with propargyl ester functional groups. In this work, further examination discovered that gold catalysts devoid of the 2-benzoylpyridine ligand (e.g., NaAuCl4) had significantly reduced levels of protein labeling. Mechanistic investigations then revealed that BPy-Au and propargyl esters undergo a rare example of C(sp )-C(sp) aryl-alkynyl cross-coupling, likely through spontaneous reductive elimination. Overall, these observations appear to suggest that BPy-Au-mediated, propargyl ester-based protein labeling acts via an activated ester intermediate, which contributes to our understanding of this process and will aid the expansion/optimization of gold-catalyst usage in future bioconjugation applications, especially in vivo.

摘要

在之前的报告工作中,Au 配合物与 2-苯甲酰吡啶配体 BPy-Au 预结合到蛋白质上,并用于发现具有炔丙基酯官能团的新型蛋白质导向标记方法。在这项工作中,进一步的研究发现,没有 2-苯甲酰吡啶配体的金催化剂(例如 NaAuCl4)对蛋白质的标记水平显著降低。然后,机理研究表明 BPy-Au 和炔丙基酯经历了罕见的 C(sp )-C(sp)芳基-炔基交叉偶联,可能是通过自发的还原消除。总的来说,这些观察结果似乎表明,BPy-Au 介导的基于炔丙基酯的蛋白质标记通过活化酯中间体起作用,这有助于我们理解这一过程,并将有助于未来生物缀合应用中扩大/优化金催化剂的使用,特别是在体内。

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