A plethora of both experimental and computational methods have been proposed in the past 20 years for the identification of hot spots at a protein-protein interface. The experimental determination of a protein-protein complex followed by alanine scanning mutagenesis, though able to determine hot spots with much precision, is expensive and has no guarantee of success while the accuracy of the current computational methods for hot-spot identification remains low. Here, we present a novel structure-based computational approach that accurately determines hot spots through docking into a set of proteins homologous to only one of the two interacting partners of a compound capable of disrupting the protein-protein interaction (PPI).
View Article and Find Full Text PDFThe estimation of clamping force has been regarded as the main issue in the maintenance of high-tension bolts. This paper proposes a method which uses the dependency of ultrasonic velocity on stress based on the nonlinear elastic effect. The variation of ultrasonic velocity in the range of actual stress acting in the bolt is very small so that the precise measurement of ultrasonic velocity is needed.
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