Lanthanide binding peptide surfactants at air–aqueous interfaces for interfacial separation of rare earth elements

Journal Article · 19 December 2024 · Proceedings of the National Academy of Sciences of the United States of America

DOI: https://doi.org/10.1073/pnas.2411763121 · OSTI ID:2483379

Ortuno Macias, Luis E. ; Jiménez-Ángeles, Felipe ; Marmorstein, Jason G.; Wang, Yiming ; Crane, Stephen A.; K. T., Surabh ; Sun, Pan; Sapkota, Bikash ; Hummingbird, Eshe; Jung, Woojin; Qiao, Baofu ; Lee, Daeyeon; Dmochowski, Ivan J.; Messinger, Robert J.; Schlossman, Mark L. ; de la Fuente-Nunez, Cesar; Radhakrishnan, Ravi ; Petersson, E. James; Olvera de la Cruz, Monica ; Bu, Wei ; Bera, Mrinal ; Lin, Binhua ; Tu, Raymond S. ; Stebe, Kathleen J.; Maldarelli, Charles

Rare earth elements (REEs) are critical materials to modern technologies. They are obtained by selective separation from mining feedstocks consisting of mixtures of their trivalent cation. We are developing an all-aqueous, bioinspired, interfacial separation using peptides as amphiphilic molecular extractants. Lanthanide binding tags (LBTs) are amphiphilic peptide sequences based on the EF-hand metal binding loops of calcium-binding proteins which complex selectively REEs. We study LBTs optimized for coordination to Tb ³⁺ using luminescence spectroscopy, surface tensiometry, X-ray reflectivity, and X-ray fluorescence near total reflection, and find that these LBTs capture Tb ³⁺ in bulk and adsorb the complex to the interface. Molecular dynamics show that the binding pocket remains intact upon adsorption. We find that, if the net negative charge on the peptide results in a negatively charged complex, excess cations are recruited to the interface by nonselective Coulombic interactions that compromise selective REE capture. If, however, the net negative charge on the peptide is −3, resulting in a neutral complex, a 1:1 surface ratio of cation to peptide is achieved. Surface adsorption of the neutral peptide complexes from an equimolar mixture of Tb ³⁺ and La ³⁺ demonstrates a switchable platform dictated by bulk and interfacial effects. The adsorption layer becomes enriched in the favored Tb ³⁺ when the bulk peptide is saturated, but selective to La ³⁺ for undersaturation due to a higher surface activity of the La ³⁺ complex.

• Sponsoring Organization: USDOE
• Grant/Contract Number: AC02-06CH11357; SC0022240
• OSTI ID: 2483379
• Journal Information: Proceedings of the National Academy of Sciences of the United States of America, Journal Name: Proceedings of the National Academy of Sciences of the United States of America Journal Issue: 52 Vol. 121; ISSN 0027-8424
• Publisher: Proceedings of the National Academy of SciencesCopyright Statement
• Country of Publication: United States
• Language: English