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Classical CBM-cellulose pull-down assays, depending on the adsorption model fitted, predicted between 1.2 to 7-fold reduction in CBM1 binding affinity for cellulose III. Force spectroscopy measurements of CBM1-cellulose interactions, along with molecular dynamics simulations, indicated that previous interpretations of classical binding assay results using multi-site adsorption models may have complicated analysis, and instead suggest simpler single-site models should be used. These findings were corroborated by binding

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We computed two time-domain indices, the skin conductance level (SCL) and nonspecific skin conductance responses (NS.SCRs), and two spectral indices, the normalized sympathetic components of the EDA (EDASympn), and the time-varying EDA index of sympathetic control (TVSymp). The results showed similar performances for EDASympn and TVSymp indices across both devices. While spectral indices obtained from both devices performed similarly in response to orthostatic and cognitive stress, time-domain exhibited large variation when obtained by