Emerging role of carbonyl –carbonyl interactions in the classification of beta turns

AbstractCarbonyl –carbonyl interactions in peptides and proteins attracted considerable interest in recent years. Here, we report a survey of carbonyl–carbonyl interactions in cyclic peptides, depsipeptides, peptoids and discuss the relationship between backbone torsion angles and CO∙∙∙CO distances. In gen eral, φ values in the range between −40° and −90° and between 40° and 90° correspond to CO∙∙∙CO distances below 3.22 Å. By extending the analysis of carbonyl–carbonyl interactions in different types of beta turns in proteins, we also highlight the role of direct or reciprocal car bonyl–carbonyl interactions in stabilizing the beta turn conformation for each specific type. We confirmed the new type II beta turn, detected by Dunbrack and coworkers, and named Pa, and detect the presence of a direct carbonyl–carbonyl interaction between the second and third residues of the t urn. We also evidenced the existence of another new type II beta turn, named pA (following Dunbrack's notation), which represents the alternative conformation of Pa with opposite φ and ψ values and is characterized by a direct carbonyl–carbonyl interaction between the second and third residues o f the turn. Finally, we show that the occurrence of CO∙∙∙CO interactions could be also advocated to explain from a chemical point of view the diversity of turn types.
Source: Protein Science - Category: Biochemistry Authors: Tags: RESEARCH ARTICLE Source Type: research