Nature Chemical BiologyBioengineeringPeer-reviewed journal article
A family portrait of lanmodulin selectivity for enhanced rare-earth separations
Patrick DiepiD, Cody S. MadseniD, Wonseok ChoiiD, Ziye DongiD, Christina S. Kang-YuniD, Patricia F.V. Uychoco, Jeremy A. SeideliD, Samuel A. EatoniD, Yongqin JiaoiD, Joseph Alfred CotruvoiD, D M ParkiD
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 fine-tune metalloprotein selectivity are bottlenecked 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 dampened selectivity for 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.
- assay: proteomics
- research focus: protein folding & dynamics
- research focus: drug response / drug discovery
- research focus: benchmarking
- approach: experimental assay
- Citations
- 7
- FWCI
- 14.36
- Field percentile
- top 1%
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