4.8 Article

Probing Lanmodulin's Lanthanide Recognition via Sensitized Luminescence Yields a Platform for Quantification of Terbium in Acid Mine Drainage

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 143, Issue 35, Pages 14287-14299

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.1c06360

Keywords

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Funding

  1. National Science Foundation [CHE-1945015]
  2. Penn State University (a Lab Bench to Commercialization grant)
  3. Penn State University (Louis Martarano Career Development Professorship)
  4. Penn State University (Erickson Discovery Grant)

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Lanmodulin is a natural macro-chelator with high affinity towards lanthanides, successfully developed as a biosensor for terbium detection in environmental samples. Despite ordinary metal coordination properties, its nearly diffusion-limited metal association rate sets lanmodulin apart from other EF hands, showcasing its potential for rapid and selective sensing of lanthanides in diverse applications.
Lanmodulin is the first natural, selective macro-chelator for f elements-a protein that binds lanthanides with picomolar affinity at 3 EF hands, motifs that instead bind calcium in most other proteins. Here, we use sensitized terbium luminescence to probe the mechanism of lanthanide recognition by this protein as well as to develop a terbium-specific biosensor that can be applied directly in environmental samples. By incorporating tryptophan residues into specific EF hands, we infer the order of metal binding of these three sites. Despite lanmodulin's remarkable lanthanide binding properties, its coordination of approximately two solvent molecules per site (by luminescence lifetime) and metal dissociation kinetics (k(off) = 0.02-0.05 s(-1), by stopped-flow fluorescence) are revealed to be rather ordinary among EF hands; what sets lanmodulin apart is that metal association is nearly diffusion limited (k(on) approximate to 10(9) M-1 s(-1)). Finally, we show that Trp-substituted lanmodulin can quantify 3 ppb (18 nM) terbium directly in acid mine drainage at pH 3.2 in the presence of a 100-fold excess of other rare earths and a 100 000-fold excess of other metals using a plate reader. These studies not only yield insight into lanmodulin's mechanism of lanthanide recognition and the structures of its metal binding sites but also show that this protein's unique combination of affinity and selectivity outperforms synthetic luminescence-based sensors, opening the door to rapid and inexpensive methods for selective sensing of individual lanthanides in the environment and in-line monitoring in industrial operations.

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