Phage display identifies Affimer proteins that direct calcium carbonate polymorph formation
Ilaria Sandei, Thembaninkosi Gaule, Matthew Batchelor, Emanuele Paci, Yi-Yeoun Kim, Alexander N. Kulak, Darren C. Tomlinson, Fiona C. Meldrum

TL;DR
Scientists used phage display to find proteins that can control the formation of different calcium carbonate minerals, showing how protein shape and magnesium ions influence mineral types.
Contribution
This study introduces the use of full proteins (Affimers) instead of short peptides in phage display to control calcium carbonate polymorph formation.
Findings
Two aragonite-binding proteins produced aragonite in a 1:1 calcium-magnesium ratio.
Calcite-binding proteins generated magnesium-calcite under the same conditions.
Molecular dynamics simulations showed protein conformation and magnesium ions are key to polymorph control.
Abstract
A key factor in biomineralization is the use of organic molecules to direct the formation of inorganic materials. However, identification of molecules that can selectively produce the calcium carbonate polymorphs calcite or aragonite has proven extremely challenging. Here, we use a phage display approach to identify proteins – rather than the short peptides typically identified using this method – that can direct calcium carbonate formation. A 1.3 × 1010 library of Affimer proteins was displayed on modified M13 phage, where an Affimer is a ≈13 kDa protein scaffold that displays two variable regions of 9–13 residues. The phage displaying the Affimer library were then screened in binding assays against calcite and aragonite at pH 7.4, and four different strongly-binding proteins were identified. The two aragonite-binding proteins generated aragonite when calcium and magnesium ions were…
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Taxonomy
TopicsCalcium Carbonate Crystallization and Inhibition · Enzyme function and inhibition · Enzyme Structure and Function
