Single-molecule force spectroscopy reveals a mechanically stable protein fold and the rational tuning of its mechanical stability.

ABSTRACT: It is recognized that shear topology of two directly connected force-bearing terminal beta-strands is a common feature among the vast majority of mechanically stable proteins known so far. However, these proteins belong to only two distinct protein folds, Ig-like beta sandwich fold and beta-grasp fold, significantly hindering delineating molecular determinants of mechanical stability and rational tuning of mechanical properties. Here we combine single-molecule atomic force microscopy and steered molecular dynamics simulation to reveal that the de novo designed Top7 fold [Kuhlman B, Dantas G, Ireton GC, Varani G, Stoddard BL, Baker D (2003) Science 302:1364-1368] represents a mechanically stable protein fold that is distinct from Ig-like beta sandwich and beta-grasp folds. Although the two

SUBMITTER: Sharma D 

PROVIDER: S-EPMC1890485 | biostudies-literature | 2007 May

REPOSITORIES: biostudies-literature