Observing reorientation dynamics with Time-Resolved fluorescence and molecular dynamics in varying periodic boundary conditions

• Published in: Journal of biomolecular structure & dynamics Vol. 40; no. 21; pp. 10614 - 10628
• Main Authors: Jas, Gouri S., Childs, Ed W., Middaugh, C. Russell, Kuczera, Krzysztof
• Format: Journal Article
• Language: English
• Published: England Taylor & Francis 01.01.2022
• Subjects: Diffusion; Flavin-Adenine Dinucleotide; kinetics; Molecular Dynamics Simulation; molecular dynamics simulations; optimum dimensionality reduction; Peptides; periodic boundary conditions; Time-resolved fluorescence; Water - chemistry; molecular dynamics simulations; periodic boundary conditions; kinetics; Time-resolved fluorescence; optimum dimensionality reduction
• ISSN: 0739-1102; 1538-0254
• DOI: 10.1080/07391102.2021.1947894

This work presents a combined study of time-resolved fluorescence spectroscopy and all-atom molecular dynamics simulation to investigate periodic boundary conditions' and water models' influence on the orientation dynamics and translational and rotational diffusion of peptides in solution. We have characterized the effects of solvent box size and water model choice on the dynamics of two peptide systems, NATA and WK5. Computationally, translational, and rotational diffusion and internal fluctuations are investigated through all-atom molecular dynamics simulation with two water models and different box sizes. These results are compared with time-resolved fluorescence anisotropy decay (FAD) measurements. The associated time constant and orientation dynamics from FAD measurement along the 1 L b axis provided baseline data to validate molecular dynamics simulation. The modeling results show that diffusion rates vary roughly in inverse proportion to water model viscosity, as one would expect. Corrections for finite box size are significant for translational diffusion and insignificant for rotational diffusion. This study also finds that internal dynamics described by autocorrelation functions and kinetic network models are relatively insensitive to both box size and water model properties. Our observation suggests that different peptide properties respond differently to a change in simulation conditions. Communicated by Ramaswamy H. Sarma