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Use of Molecular Modeling to Design Selective NTS2 Neurotensin Analogues.

Roberto FanelliNicolas FloquetÉlie Besserer-OffroyBartholomé DelortMélanie VivancosJean-Michel LongpréPedro RenaultMathéo BerthetPhilippe SarretFlorine Cavelier
Published in: Journal of medicinal chemistry (2017)
Neurotensin exerts potent analgesia by acting at both NTS1 and NTS2 receptors, whereas NTS1 activation also results in other physiological effects such as hypotension and hypothermia. Here, we used molecular modeling approach to design highly selective NTS2 ligands by investigating the docking of novel NT[8-13] compounds at both NTS1 and NTS2 sites. Molecular dynamics simulations revealed an interaction of the Tyr11 residue of NT[8-13] with an acidic residue (Glu179) located in the ECL2 of hNTS2 or with a basic residue (Arg212) at the same position in hNTS1. The importance of the residue at position 11 for NTS1/NTS2 selectivity was further demonstrated by the design of new NT analogues bearing basic (Lys, Orn) or acid (Asp or Glu) function. As predicted by the molecular dynamics simulations, binding of NT[8-13] analogues harboring a Lys11 exhibited higher affinity toward the hNTS1-R212E mutant receptor, in which Arg212 was substituted by the negatively charged Glu residue.
Keyphrases
  • molecular dynamics simulations
  • molecular docking
  • cardiac arrest
  • amino acid
  • brain injury
  • small molecule
  • single cell
  • chronic pain
  • protein protein
  • ultrasound guided