Capturing an elusive but critical element: Natural protein enables actinium chemistry

Gauthier J.P. Deblonde, Joseph A. Mattocks, Ziye Dong, Paul T. Wooddy, Joseph A. Cotruvo, Mavrik Zavarin

Research output: Contribution to journalArticlepeer-review

16 Scopus citations

Abstract

Actinium-based therapies could revolutionize cancer medicine but remain tantalizing due to the difficulties in studying and limited knowledge of Ac chemistry. Current efforts focus on small synthetic chelators, limiting radioisotope complexation and purification efficiencies. Here, we demonstrate a straightforward strategy to purify medically relevant radiometals, actinium(III) and yttrium(III), and probe their chemistry, using the recently discovered protein, lanmodulin. The stoichiometry, solution behavior, and formation constant of the 228Ac3+-lanmodulin complex and its 90Y3+/natY3+/natLa3+ analogs were experimentally determined, representing the first actinium-protein and strongest actinide(III)-protein complex (sub-picomolar Kd) to be characterized. Lanmodulin's unparalleled properties enable the facile purification recovery of radiometals, even in the presence of >10+10 equivalents of competing ions and at ultratrace levels: down to 2 femtograms 90Y3+ and 40 attograms 228Ac3+. The lanmodulin-based approach charts a new course to study elusive isotopes and develop versatile chelating platforms for medical radiometals, both for high-value separations and potential in vivo applications.

Original languageEnglish (US)
Article numbereabk0273
JournalScience Advances
Volume7
Issue number43
DOIs
StatePublished - Oct 2021

All Science Journal Classification (ASJC) codes

  • General

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