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探测金属与藻胆蛋白的结合。

Probing heavy metal binding to phycobiliproteins.

机构信息

School of Biosciences, University of Birmingham, UK.

出版信息

FEBS J. 2022 Aug;289(15):4646-4656. doi: 10.1111/febs.16396. Epub 2022 Feb 22.

Abstract

Blue-green algae, also known as cyanobacteria, contain some of the most efficient light-harvesting complexes known. These large, colourful complexes consist of phycobiliproteins which are extremely valuable in the cosmetics, food, nutraceutical and pharmaceutical industries. Additionally, the colourful and fluorescent properties of phycobiliproteins can be modulated by metal ions, making them highly attractive as heavy metal sensors and heavy metal scavengers. Although the overall quenching ability metal ions have on phycobiliproteins is known, the mechanism of heavy metal binding to phycobiliproteins is not fully understood, limiting their widespread quantitative applications. Here, we show using high-resolution native mass spectrometry that phycobiliprotein complexes bind metal ions in different manners. Through monitoring the binding equilibria and metal-binding stoichiometry, we show in particular copper and silver to have drastic, yet different effects on phycobiliprotein structure, both copper and silver modulate the overall complex properties. Together, the data reveals the mechanisms by which metal ions can modulate phycobiliprotein properties which can be used as a basis for the future design of metal-related phycobiliprotein applications.

摘要

蓝绿藻,又称蓝细菌,含有一些已知的最高效的光捕获复合物。这些大型、多彩的复合物由藻胆蛋白组成,在化妆品、食品、营养保健品和制药行业极具价值。此外,藻胆蛋白的彩色和荧光特性可以通过金属离子进行调节,使它们成为极具吸引力的重金属传感器和重金属清除剂。尽管人们已经了解金属离子对藻胆蛋白整体的淬灭能力,但重金属与藻胆蛋白结合的机制尚未完全阐明,限制了它们在广泛的定量应用中使用。在这里,我们使用高分辨率 native mass 质谱法表明,藻胆蛋白复合物以不同的方式结合金属离子。通过监测结合平衡和金属结合化学计量,我们特别表明铜和银对藻胆蛋白结构有剧烈但不同的影响,铜和银都调节整体复合物性质。总之,这些数据揭示了金属离子调节藻胆蛋白性质的机制,可作为未来设计与金属相关的藻胆蛋白应用的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0d6/9542875/1717d2a22230/FEBS-289-4646-g006.jpg

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