Unveiling POM–peptide complexes: molecular insights into metal oxide nanoparticle–protein interactions

IF 2.6 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
CrystEngComm Pub Date : 2025-02-25 DOI:10.1039/D4CE01269K
Björn H. Greijer and Vadim G. Kessler
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引用次数: 0

Abstract

Mineral nanoparticles (NPs) play a crucial role in biological systems, exhibiting enzyme-like “nanozyme” activity in protein oxidation and hydrolysis. To study NP interactions at the molecular level, we characterized complexes of peptides with poly-oxo-metalate (POM) species, the smallest known NPs. Our findings highlight the importance of factors such as metal–oxygen bond polarity, peptide hydrophilicity, medium conditions, and structure-directing amino acids. Using single-crystal models and 2D NMR, we also explored interactions between larger NPs as nanozymes and proteins relevant for specific oxidation of amino acids and proteins.

Abstract Image

揭示pom肽复合物:分子洞察金属氧化物纳米颗粒-蛋白质相互作用
矿物纳米颗粒(NPs)在生物系统中发挥着至关重要的作用,在蛋白质氧化和水解中表现出类似酶的“纳米酶”活性。为了在分子水平上研究NP相互作用,我们表征了多肽与聚氧金属酸盐(POM)的复合物,这是已知最小的NP。我们的发现强调了诸如金属-氧键极性、肽亲水性、介质条件和结构导向氨基酸等因素的重要性。利用单晶模型和二维核磁共振,我们还探索了作为纳米酶的较大NPs与氨基酸和蛋白质特定氧化相关的蛋白质之间的相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CrystEngComm
CrystEngComm 化学-化学综合
CiteScore
5.50
自引率
9.70%
发文量
747
审稿时长
1.7 months
期刊介绍: Design and understanding of solid-state and crystalline materials
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