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8UYN

Fundamental Characterization of Chelated and Crystallized Actinium in a Macromolecular Host

Summary for 8UYN
Entry DOI10.2210/pdb8uyn/pdb
DescriptorNeutrophil gelatinase-associated lipocalin, LANTHANUM (III) ION, N,N'-butane-1,4-diylbis[1-hydroxy-N-(3-{[(1-hydroxy-6-oxo-1,6-dihydropyridin-2-yl)carbonyl]amino}propyl)-6-oxo-1,6-dihydropyridine-2-carboxamide], ... (6 entities in total)
Functional Keywordsinhibitor, metal binding protein
Biological sourceHomo sapiens (human)
Total number of polymer chains3
Total formula weight64736.60
Authors
Rupert, P.B.,Strong, R.K. (deposition date: 2023-11-13, release date: 2024-09-25, Last modification date: 2024-11-20)
Primary citationWacker, J.N.,Woods, J.J.,Rupert, P.B.,Peterson, A.,Allaire, M.,Lukens, W.W.,Gaiser, A.N.,Minasian, S.G.,Strong, R.K.,Abergel, R.J.
Actinium chelation and crystallization in a macromolecular scaffold.
Nat Commun, 15:5741-5741, 2024
Cited by
PubMed Abstract: Targeted alpha therapy (TAT) pairs the specificity of antigen targeting with the lethality of alpha particles to eradicate cancerous cells. Actinium-225 [Ac; t = 9.920(3) days] is an alpha-emitting radioisotope driving the next generation of TAT radiopharmaceuticals. Despite promising clinical results, a fundamental understanding of Ac coordination chemistry lags behind the rest of the Periodic Table due to its limited availability, lack of stable isotopes, and inadequate systems poised to probe the chemical behavior of this radionuclide. In this work, we demonstrate a platform that combines an 8-coordinate synthetic ligand and a mammalian protein to characterize the solution and solid-state behavior of the longest-lived Ac isotope, Ac [t = 21.772(3) years]. We expect these results to direct renewed efforts for Ac-TAT development, aid in understanding Ac coordination behavior relative to other +3 lanthanides and actinides, and more broadly inform this element's position on the Periodic Table.
PubMed: 39009580
DOI: 10.1038/s41467-024-50017-5
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2 Å)
Structure validation

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