E. R. Lovyagina, A. V. Loktyushkin, N. S. Vasiliev, B. K. Semin
{"title":"Mechanism of Inhibition of the Oxygen-Evolving Complex of Photosystem II by Lanthanide Cations","authors":"E. R. Lovyagina, A. V. Loktyushkin, N. S. Vasiliev, B. K. Semin","doi":"10.1134/S0006350923040103","DOIUrl":null,"url":null,"abstract":"<p>The interaction of La<sup>3+</sup> and Tb<sup>3+</sup> cations with the Ca-binding site of the oxygen-evolving complex of photosystem II samples depleted of calcium has been studied. The binding of cations to the Ca-binding site is irreversible and the bound cations cannot be washed out or replaced by Ca<sup>2+</sup> cations. The feature of lanthanides to bind strongly to the Ca-binding site was used to investigate whether the bound Ln<sup>3+</sup> cation has an effect on the high-affinity Mn-binding site of the oxygen-evolving complex. For this purpose, hydroquinone was used to extract manganese cations from the oxygen-evolving complex of the calcium-depleted photosystem II membranes with the Ca-binding site blocked by La<sup>3+</sup> or Tb<sup>3+</sup>, and the activity of the high-affinity site was then examined using exogenous electron donors (Mn<sup>2+</sup> + H<sub>2</sub>O<sub>2</sub>) and 1,5-diphenylcarbazide. It was found that lanthanide cations bound to the Ca-binding site significantly inhibited oxidation of electron donors through the high-affinity Mn-binding site. The mechanism of the observed effect is discussed.</p>","PeriodicalId":493,"journal":{"name":"Biophysics","volume":"68 4","pages":"519 - 524"},"PeriodicalIF":4.0330,"publicationDate":"2023-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biophysics","FirstCategoryId":"4","ListUrlMain":"https://link.springer.com/article/10.1134/S0006350923040103","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 0
Abstract
The interaction of La3+ and Tb3+ cations with the Ca-binding site of the oxygen-evolving complex of photosystem II samples depleted of calcium has been studied. The binding of cations to the Ca-binding site is irreversible and the bound cations cannot be washed out or replaced by Ca2+ cations. The feature of lanthanides to bind strongly to the Ca-binding site was used to investigate whether the bound Ln3+ cation has an effect on the high-affinity Mn-binding site of the oxygen-evolving complex. For this purpose, hydroquinone was used to extract manganese cations from the oxygen-evolving complex of the calcium-depleted photosystem II membranes with the Ca-binding site blocked by La3+ or Tb3+, and the activity of the high-affinity site was then examined using exogenous electron donors (Mn2+ + H2O2) and 1,5-diphenylcarbazide. It was found that lanthanide cations bound to the Ca-binding site significantly inhibited oxidation of electron donors through the high-affinity Mn-binding site. The mechanism of the observed effect is discussed.
BiophysicsBiochemistry, Genetics and Molecular Biology-Biophysics
CiteScore
1.20
自引率
0.00%
发文量
67
期刊介绍:
Biophysics is a multidisciplinary international peer reviewed journal that covers a wide scope of problems related to the main physical mechanisms of processes taking place at different organization levels in biosystems. It includes structure and dynamics of macromolecules, cells and tissues; the influence of environment; energy transformation and transfer; thermodynamics; biological motility; population dynamics and cell differentiation modeling; biomechanics and tissue rheology; nonlinear phenomena, mathematical and cybernetics modeling of complex systems; and computational biology. The journal publishes short communications devoted and review articles.