Conformational analysis on anti-HIV-1 peptide T22([Tyr5,12,Lys7]-polyphemusinⅡ )

The conformational scan of anti-HIV peptide T22 ([Tyrsup>5,12, Lys⁷]-polyphemusinⅡ) backbone on a deformed potential energy surface (PES) was performed using the potential smoothing searching (PSS) protocol. All located minima were then transferred to the original PES using undeformed optimized potentials for liquid simulations (OPLS) potential function, and minimized by multi-conformer minimization (MCM). For solution-phase calculations, the GB/SA continuum model for water was used. This application of PSS integrated with MCM is proved a feasible method for solving the multiple-minimum problem in the conformational analysis of flexible molecules with cyclic structure.