Nature Communications (May 2020)

DIP/Dpr interactions and the evolutionary design of specificity in protein families

  • Alina P. Sergeeva,
  • Phinikoula S. Katsamba,
  • Filip Cosmanescu,
  • Joshua J. Brewer,
  • Goran Ahlsen,
  • Seetha Mannepalli,
  • Lawrence Shapiro,
  • Barry Honig

DOI
https://doi.org/10.1038/s41467-020-15981-8
Journal volume & issue
Vol. 11, no. 1
pp. 1 – 14

Abstract

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Dpr (Defective proboscis extension response) and DIP (Dpr Interacting Proteins) are immunoglobulin-like cell-cell adhesion proteins that form highly specific pairwise interactions, which control synaptic connectivity during Drosophila development. Here, the authors combine a computational approach with binding affinity measurements and find that DIP/Dpr binding specificity is controlled by negative constraints that interfere with non-cognate binding.