Effect of C-terminal sequence on competitive semaphorin binding to neuropilin-1

Matthew W. Parker, Andrew D. Linkugel, Craig W. Vander Kooi

Research output: Contribution to journalArticlepeer-review

25 Scopus citations

Abstract

Neuropilins (Nrp) are type I transmembrane proteins that function as receptors for vascular endothelial growth factor (VEGF) and class III Semaphorin (Sema3) ligand families. Sema3s function as potent endogenous angiogenesis inhibitors but require proteolytically processing by furin to compete with VEGF for Nrp binding. This processing liberates a C-terminal arginine (CR) that is necessary for binding to the b1 domain of Nrp, a common feature shared by Nrp ligands. The CR is necessary but not sufficient for potent Nrp inhibition, and the role of upstream residues is unknown. We demonstrate that the second-to-last residue (C-1), immediately upstream of the CR, plays a significant role in controlling competitive ligand binding by orienting the C-terminus for productive Nrp binding. With the use of a peptide library derived from Sema3F, C-1 residues that preferentially adopt an extended bound-like conformation, including proline and β-branched amino acids, were found to produce the most avid competitors. Consistent with this, analysis of the binding thermodynamics revealed that more favorable entropy is responsible for the observed binding enhancement of C-1 proline. We further tested the effect of the C-1 residue on Sema3F processing by furin and found an inverse relationship between processing and inhibitory potency. Analysis of all Sema3 family members reveals two non-equivalent furin processing sites differentiated by the presence of either a C-1 proline or a C-1 arginine and resulting in up to a 40-fold difference in potency. These data reveal a novel regulatory mechanism of Sema3 activity and define a fundamental mechanism for preferential Nrp binding.

Original languageEnglish (US)
Pages (from-to)4405-4414
Number of pages10
JournalJournal of Molecular Biology
Volume425
Issue number22
DOIs
StatePublished - Nov 15 2013
Externally publishedYes

Keywords

  • VEGF
  • angiogenesis
  • furin
  • peptide library
  • proteolysis

ASJC Scopus subject areas

  • Structural Biology
  • Molecular Biology

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