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植物螯合肽与锌(II)结合的亲和力为微摩尔至皮摩尔级,不会形成双核配合物,表现出锌缓冲和消音器功能,而不是存储功能。

Phytochelatins Bind Zn(II) with Micro- to Picomolar Affinities without the Formation of Binuclear Complexes, Exhibiting Zinc Buffering and Muffling Rather than Storing Functions.

机构信息

Department of Chemical Biology, Faculty of Biotechnology, University of Wrocław, Joliot-Curie 14a, 50-383 Wrocław, Poland.

Department of Plant Physiology, Faculty of Biology, Chemistry and Earth Sciences, University of Bayreuth, 95440 Bayreuth, Germany.

出版信息

Inorg Chem. 2024 Jun 17;63(24):10915-10931. doi: 10.1021/acs.inorgchem.4c01707. Epub 2024 Jun 6.

Abstract

Phytochelatins (PCs) are poly-Cys peptides containing a repeating γ-Glu-Cys motif synthesized in plants, algae, certain fungi, and worms by PC synthase from reduced glutathione. It has been shown that an excess of toxic metal ions induces their biosynthesis and that they are responsible for the detoxification process. Little is known about their participation in essential metal binding under nontoxic, basal conditions under which PC synthase is active. This study presents spectroscopic and thermodynamic interactions with the PC2-PC5 series, mainly focusing on the relations between Zn(II) complex stability and cellular Zn(II) availability. The investigations employed mass spectrometry, UV-vis spectroscopy, potentiometry, competition assays with zinc probes, and isothermal titration calorimetry (ITC). All peptides form ZnL complexes, while ZnL was found only for PC2, containing two to four sulfur donors in the coordination sphere. Binuclear species typical of Cd(II)-PC complexes are not formed in the case of Zn(II). Results demonstrate that the affinity for Zn(II) increases linearly from PC2 to PC4, ranging from micro- to low-picomolar. Further elongation does not significantly increase the stability. Stability elevation is driven mainly by entropic factors related to the chelate effect and conformational restriction rather than enthalpic factors related to the increasing number of sulfur donors. The affinity of the investigated PCs falls within the range of exchangeable Zn(II) concentrations (hundreds of pM) observed in plants, supporting for the first time a role of PCs both in buffering and in muffling cytosolic Zn(II) concentrations under normal conditions, not exposed to zinc excess, where short PCs have been identified in numerous studies. Furthermore, we found that Cd(II)-PC complexes demonstrate significantly higher metal capacities due to the formation of polynuclear species, which are lacking for Zn(II), supporting the role of PCs in Cd(II) storage (detoxification) and Zn(II) buffering and muffling. Our results on phytochelatins' coordination chemistry and thermodynamics are important for zinc biology and understanding the molecular basis of cadmium toxicity, leaving room for future studies.

摘要

植物螯合肽(PCs)是一类富含半胱氨酸的多肽,含有重复的γ-Glu-Cys 基序,由植物、藻类、某些真菌和蠕虫中的 PC 合酶利用还原型谷胱甘肽合成。已有研究表明,有毒金属离子的过量会诱导其生物合成,并且它们负责解毒过程。在无毒、基础条件下,PC 合酶活性较高,PC 参与必需金属结合的情况知之甚少。本研究主要关注 Zn(II)配合物稳定性与细胞内 Zn(II)可用性之间的关系,对 PC2-PC5 系列进行了光谱和热力学相互作用研究。研究采用了质谱、紫外可见光谱、电位法、锌探针竞争实验和等温滴定量热法(ITC)。所有肽都形成了 ZnL 配合物,而 ZnL 仅存在于含有两个到四个配位硫原子的 PC2 中。在 Zn(II)的情况下,没有形成典型的 Cd(II)-PC 配合物的双核物种。结果表明,对 Zn(II)的亲和力从 PC2 到 PC4 线性增加,范围从微摩尔到低皮摩尔。进一步延伸不会显著增加稳定性。稳定性的提高主要由熵因素驱动,与螯合效应和构象限制有关,而不是与增加的硫供体数量有关的焓因素。所研究的 PCs 的亲和力落在植物中观察到的可交换 Zn(II)浓度(数百皮摩尔)范围内,首次支持 PCs 在缓冲和缓和正常条件下(未暴露于锌过量)的细胞溶质 Zn(II)浓度方面的作用,在许多研究中已鉴定出短 PC。此外,我们发现由于形成多核物种,Cd(II)-PC 配合物表现出更高的金属容量,而 Zn(II) 则没有形成多核物种,这支持了 PCs 在 Cd(II)存储(解毒)和 Zn(II)缓冲和缓和方面的作用。我们关于植物螯合肽的配位化学和热力学的研究结果对锌生物学和理解镉毒性的分子基础很重要,为未来的研究留下了空间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d6d/11191002/3bbb3cf7b56b/ic4c01707_0010.jpg

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