We present a detailed study of the performance and reliability of design procedures based on energy minimization. The analysis is carried out for model proteins where exact results can be obtained through exhaustive enumeration. The efficiency of design techniques is assessed as a function of protein length and the number of classes into which amino acids are coarse grained. It turns out that, while energy minimization strategies can identify correct solutions in most circumstances, it may be impossible for numerical implementations of design algorithms to meet the efficiency required to yield correct solutions in realistic contexts. Alternative design strategies based on an approximate treatment of the free energy are shown to be much more efficient than energy-based methods while requiring nearly the same CPU time. Finally, we present a novel iterative design strategy that incorporates negative design with the use of selected decoy structures that compete significantly with the target native state in housing the designed sequences. This procedure allows one to identify systematically all sequences that fold on a given target structure.
|Titolo:||A comparative study of existing and new design techniques for protein models|
|Autori:||MICHELETTI C; A. MARITAN; J.R. BANAVAR|
|Rivista:||THE JOURNAL OF CHEMICAL PHYSICS|
|Data di pubblicazione:||1999|
|Digital Object Identifier (DOI):||10.1063/1.478938|
|Appare nelle tipologie:||1.1 Journal article|