Structural basis for distinct functions of the naturally occurring Cys mutants of human apolipoprotein A-I

J Lipid Res. 2013 Dec;54(12):3244-57. doi: 10.1194/jlr.R037911. Epub 2013 Sep 13.

Abstract

HDL removes cell cholesterol and protects against atherosclerosis. ApoA-I provides a flexible structural scaffold and an important functional ligand on the HDL surface. We propose structural models for apoA-I(Milano) (R173C) and apoA-I(Paris) (R151C) mutants that show high cardioprotection despite low HDL levels. Previous studies established that two apoA-I molecules encircle HDL in an antiparallel, helical double-belt conformation. Recently, we solved the atomic structure of lipid-free Δ(185-243)apoA-I and proposed a conformational ensemble for apoA-I(WT) on HDL. Here we modify this ensemble to understand how intermolecular disulfides involving C173 or C151 influence protein conformation. The double-belt conformations are modified by belt rotation, main-chain unhinging around Gly, and Pro-induced helical bending, and they are verified by comparison with previous experimental studies and by molecular dynamics simulations of apoA-I(Milano) homodimer. In our models, the molecular termini repack on various-sized HDL, while packing around helix-5 in apoA-I(WT), helix-6 in apoA-I(Paris), or helix-7 in apoA-I(Milano) homodimer is largely conserved. We propose how the disulfide-induced constraints alter the protein conformation and facilitate dissociation of the C-terminal segment from HDL to recruit additional lipid. Our models unify previous studies of apoA-I(Milano) and demonstrate how the mutational effects propagate to the molecular termini, altering their conformations, dynamics, and function.

Keywords: Milano and Paris mutations; atherosclerosis; double-belt and trefoil/tetrafoil conformations; protein dynamics and function; protein-lipid interactions.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Apolipoprotein A-I / chemistry*
  • Apolipoprotein A-I / genetics
  • Apolipoprotein A-I / metabolism*
  • Cysteine / genetics*
  • Humans
  • Models, Molecular
  • Mutation*
  • Protein Multimerization
  • Protein Structure, Quaternary

Substances

  • Apolipoprotein A-I
  • Cysteine