Synthesis and secondary structure in membranes of the Bcl-2 anti-apoptotic domain BH4

J Pept Sci. 2006 Jan;12(1):58-64. doi: 10.1002/psc.686.

Abstract

Solid phase synthesis of BH4, the 26 amino-acid domain (6RTGYDNREIVMKYIHYKLSQRGYEWD31) of the anti-apoptotic Bcl-2 protein has been accomplished using Fmoc chemistry. The use of peculiar cleavage conditions provided high yields after purification such that tens to hundreds of mg could be obtained. A 15N-labelled version of the peptide could also be synthesized for NMR studies in membranes. The peptide purity was not lower than 98% as controlled by UV and MALDI-TOF mass spectrometry. The secondary structure was determined in water, trifluoroethanol (TFE) and in lipid membrane using UV circular dichroism. The peptide shows dominant beta-sheeted structures in water that convert progressively into alpha-helical features upon addition of TFE or membrane. The amphipathic character of the helix suggests that the peptide might have a structure akin to those of antimicrobial peptides upon interaction with membranes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Circular Dichroism
  • Dimyristoylphosphatidylcholine / chemistry
  • Membranes, Artificial*
  • Phosphatidylglycerols / chemistry
  • Protein Engineering / methods
  • Protein Structure, Secondary
  • Protein Structure, Tertiary
  • Proto-Oncogene Proteins c-bcl-2 / chemical synthesis*
  • Proto-Oncogene Proteins c-bcl-2 / chemistry*
  • Proto-Oncogene Proteins c-bcl-2 / isolation & purification
  • Solvents / chemistry
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
  • Spectrophotometry, Ultraviolet

Substances

  • Membranes, Artificial
  • Phosphatidylglycerols
  • Proto-Oncogene Proteins c-bcl-2
  • Solvents
  • dimyristoylphosphatidylglycerol
  • Dimyristoylphosphatidylcholine