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Structural characterization of actinide-calmodulin complexes by NMR spectroscopy

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  • معلومة اضافية
    • Contributors:
      Laboratory of Interactions Ligand-Actinide (LILA); Département de recherche sur les procédés pour la mine et le recyclage du combustible (DMRC); Institut des Sciences et technologies pour une Economie Circulaire des énergies bas carbone (ISEC); Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut des Sciences et technologies pour une Economie Circulaire des énergies bas carbone (ISEC); Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA); Interactions Protéine Métal (IPM); Institut de Biosciences et Biotechnologies d'Aix-Marseille (ex-IBEB) (BIAM); Aix Marseille Université (AMU)-Centre National de la Recherche Scientifique (CNRS)-Direction de Recherche Fondamentale (CEA) (DRF (CEA)); Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Aix Marseille Université (AMU)-Centre National de la Recherche Scientifique (CNRS)-Direction de Recherche Fondamentale (CEA) (DRF (CEA))
    • بيانات النشر:
      CCSD
    • الموضوع:
      2024
    • Collection:
      Aix-Marseille Université: HAL
    • الموضوع:
    • نبذة مختصرة :
      International audience ; Actinides are radioactive metals of high importance in civil and military nuclear industries. They can be found in the environment due to historical dissemination resulting from atmospheric nuclear weapon tests. Moreover, in the context of nuclear waste disposal and nuclear facilities dismantling, the handling of actinides poses a risk of contamination for the operators. Given their strong radiotoxicity, it is essential to investigate their behavior within the human body. While the targeted organs are well-known, the transport mechanism and molecular interactions remain unidentified. Proteins have b1een identified as actinide targets in the event of human contamination. Although the literature on the interactions between actinides and proteins is scarce, metalloproteomic studies have shown that several calcium-binding proteins have a strong affinity for actinides1. As a model for all calcium-binding protein, the calcium-modulated protein (calmodulin) was chosen for its EF-hand motif site, which is widely present in calcium-biding proteins. Loïc Daronnat investigated the interaction of plutonium(IV) with several variants of the calmodulin and observed various behaviors of the plutonium depending on the variant of calmodulin used2: the formation of a Pu(IV)-calmodulin complex, the formation of a Pu(III)-calmodulin complex and the formation of hexanuclear clusters of plutonium.CaME (Engineered Calmodulin) is a variant of calmodulin developed especially to bind plutonium(IV). This variant has an extra carboxylate ligand in its complexation loop (shown in figure 1), increasing its affinity for actinides IV. This particular variant was the only which did not promote the formation of plutonium clusters. Instead, it only generated 1:1 complexes. Additionally, an unexpected change of the oxidation state of plutonium (from IV to III) was noticed in presence of CaME.3 To get a better understanding of this behavior, a deepened characterization of the species formed between CaME and actinides have ...
    • الدخول الالكتروني :
      https://cea.hal.science/cea-04736404
      https://cea.hal.science/cea-04736404v1/document
      https://cea.hal.science/cea-04736404v1/file/Structural%20characterization%20of%20actinide-calmodulin%20complexes%20by%20NMR%20spectroscopy.pdf
    • Rights:
      info:eu-repo/semantics/OpenAccess
    • الرقم المعرف:
      edsbas.15918221