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A family portrait of lanmodulin selectivity for enhanced rare-earth separations

  • Patrick Diep
  • , Cody S. Madsen
  • , Wonseok Choi
  • , Ziye Dong
  • , Christina S. Kang-Yun
  • , Patricia F.V. Uychoco
  • , Jeremy A. Seidel
  • , Samuel A. Eaton
  • , Yongqin Jiao
  • , Joseph A. Cotruvo
  • , Dan M. Park

Research output: Contribution to journalArticlepeer-review

Abstract

Proteins offer a molecular design space to create bespoke ligands for the separation of critical metals like rare earth elements (REs). However, data-intensive approaches to tune metalloprotein selectivity are constrained by the low-throughput nature of existing characterization methods. Here we invented an assay called ‘SpyTag-Catcher Immobilization of Lanmodulin for Assaying Metal-Binding Selectivity’ (SpyCI-LAMBS) to measure metalloprotein selectivity en masse. This 96-format workflow was used to study the selectivity of 621 lanmodulin (LanM) orthologs for 15 REs, revealing eight distinct selectivity profiles based on sequence-to-function analyses. We discovered >200 LanMs with stronger selectivity against low-value LaIII relative to the prototypical LanM. This includes a LanM that can perform a challenging one-stage separation of PrIII from LaIII with up to >99.9 mol% purity and 83% yield. SpyCI-LAMBS is a powerful tool that can rapidly collect high-fidelity selectivity data to inform metal ion separations and machine-learning-assisted metalloprotein design. (Figure presented.)

Original languageEnglish (US)
JournalNature Chemical Biology
DOIs
StateAccepted/In press - 2026

All Science Journal Classification (ASJC) codes

  • Molecular Biology
  • Cell Biology

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