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Protein Sci. 2009 Aug;18(8):1609-19. doi: 10.1002/pro.177.

High-energy water sites determine peptide binding affinity and specificity of PDZ domains.

Author information

1
Schrödinger Inc., New York, New York 10036, USA. thijs.beuming@schrodinger.com

Abstract

PDZ domains have well known binding preferences for distinct C-terminal peptide motifs. For most PDZ domains, these motifs are of the form [S/T]-W-[I/L/V]. Although the preference for S/T has been explained by a specific hydrogen bond interaction with a histidine in the PDZ domain and the (I/L/V) is buried in a hydrophobic pocket, the mechanism for Trp specificity at the second to last position has thus far remained unknown. Here, we apply a method to compute the free energies of explicit water molecules and predict that potency gained by Trp binding is due to a favorable release of high-energy water molecules into bulk. The affinities of a series of peptides for both wild-type and mutant forms of the PDZ domain of Erbin correlate very well with the computed free energy of binding of displaced waters, suggesting a direct relationship between water displacement and peptide affinity. Finally, we show a correlation between the magnitude of the displaced water free energy and the degree of Trp-sensitivity among subtypes of the HTRA PDZ family, indicating a water-mediated mechanism for specificity of peptide binding.

PMID:
19569188
PMCID:
PMC2776949
DOI:
10.1002/pro.177
[Indexed for MEDLINE]
Free PMC Article

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