Computer simulations of the flexibility of a series of synthetic cyclic peptide analogues

Biopolymers. 1993 Aug;33(8):1249-70. doi: 10.1002/bip.360330811.

Abstract

The flexibility of a series of cyclic peptides derived from the epitope of a snake toxin is investigated using computer simulation techniques. Molecular dynamics (MD) simulations and vibrational analyses are performed on chemically constrained peptides modeled on the parent protein loop. In the 50 ps MD simulations, large variations in the atomic fluctuations are seen between the peptides, and can be related to the nature of the chemical constraints present in the molecules. Normal mode analyses are performed on energy-minimized configurations derived from the dynamics trajectories. The atomic fluctuations calculated from the normal modes are about 30% of those of the molecular dynamics for the more flexible peptides and 70% for the more constrained molecules. The calculated differences in flexibility between the molecules are much less significant in the harmonic approximation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Computer Simulation*
  • Models, Chemical*
  • Molecular Sequence Data
  • Peptides, Cyclic / chemistry*
  • Protein Conformation
  • Thermodynamics

Substances

  • Peptides, Cyclic