Sensitizing Curium Luminescence through an Antenna Protein To Investigate Biological Actinide Transport Mechanisms

• Published in: Journal of the American Chemical Society Vol. 135; no. 7; pp. 2676 - 2683
• Main Authors: Sturzbecher-Hoehne, Manuel, Goujon, Christophe, Deblonde, Gauthier J.-P, Mason, Anne B, Abergel, Rebecca J
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 20.02.2013
• Subjects: Actinoid Series Elements - chemistry; Actinoid Series Elements - metabolism; Chromatography, High Pressure Liquid; Coordination Complexes - chemistry; Curium - chemistry; Curium - metabolism; Humans; Luminescence; Thermodynamics; Transferrin - chemistry; Transferrin - metabolism
• ISSN: 0002-7863; 1520-5126
• DOI: 10.1021/ja310957f

Worldwide stocks of actinides and lanthanide fission products produced through conventional nuclear spent fuel are increasing continuously, resulting in a growing risk of environmental and human exposure to these toxic radioactive metal ions. Understanding the biomolecular pathways involved in mammalian uptake, transport and storage of these f-elements is crucial to the development of new decontamination strategies and could also be beneficial to the design of new containment and separation processes. To start unraveling these pathways, our approach takes advantage of the unique spectroscopic properties of trivalent curium. We clearly show that the human iron transporter transferrin acts as an antenna that sensitizes curium luminescence through intramolecular energy transfer. This behavior has been used to describe the coordination of curium within the two binding sites of the protein and to investigate the recognition of curium–transferrin complexes by the cognate transferrin receptor. In addition to providing the first protein–curium spectroscopic characterization, these studies prove that transferrin receptor-mediated endocytosis is a viable mechanism of intracellular entry for trivalent actinides such as curium and provide a new tool utilizing the specific luminescence of curium for the determination of other biological actinide transport mechanisms.