Engineering protein stability with atomic precision in a monomeric miniprotein

July 28, 2017

Title

Engineering protein stability with atomic precision in a monomeric miniprotein

Author

Emily G Baker, Christopher Williams, Kieran L Hudson, Gail J Bartlett, Jack W Heal, Kathryn L Porter Goff, Richard B Sessions, Matthew P Crump, Derek N Woolfson

Year

2017

Journal

Nature Chemical Biology

Abstract

Miniproteins simplify the protein-folding problem, allowing the dissection of forces that stabilize protein structures. Here we describe PPa-Tyr, a designed peptide comprising an a-helix buttressed by a polyproline II helix. PPa-Tyr is water soluble and monomeric, and it unfolds cooperatively with a midpoint unfolding temperature (TM) of 39 °C. NMR structures of PPa-Tyr reveal proline residues docked between tyrosine side chains, as designed. The stability of PPa is sensitive to modifications in the aromatic residues: replacing tyrosine with phenylalanine, i.e., changing three solvent-exposed hydroxyl groups to protons, reduces the TM to 20 °C. We attribute this result to the loss of CH–p interactions between the aromatic and proline rings, which we probe by substituting the aromatic residues with nonproteinogenic side chains. In analyses of natural protein structures, we find a preference for proline–tyrosine interactions over other proline-containing pairs, and observe abundant CH–p interactions in biologically important complexes between proline-rich ligands and SH3 and similar domains.

Instrument

J-815

Keywords

Circular dichroism, Secondary structure, Thermal stability, Thermodynamics, Tertiary structure, Protein folding, Biochemistry