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      How to learn from inconsistencies: Integrating molecular simulations with experimental data.

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          Abstract

          Molecular simulations and biophysical experiments can be used to provide independent and complementary insights into the molecular origin of biological processes. A particularly useful strategy is to use molecular simulations as a modeling tool to interpret experimental measurements, and to use experimental data to refine our biophysical models. Thus, explicit integration and synergy between molecular simulations and experiments is fundamental for furthering our understanding of biological processes. This is especially true in the case where discrepancies between measured and simulated observables emerge. In this chapter, we provide an overview of some of the core ideas behind methods that were developed to improve the consistency between experimental information and numerical predictions. We distinguish between situations where experiments are used to refine our understanding and models of specific systems, and situations where experiments are used more generally to refine transferable models. We discuss different philosophies and attempt to unify them in a single framework. Until now, such integration between experiments and simulations have mostly been applied to equilibrium data, and we discuss more recent developments aimed to analyze time-dependent or time-resolved data.

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          Author and article information

          Journal
          Prog Mol Biol Transl Sci
          Progress in molecular biology and translational science
          Elsevier BV
          1878-0814
          1877-1173
          2020
          : 170
          Affiliations
          [1 ] Structural Biology and NMR Laboratory & Linderstrøm-Lang Centre for Protein Science, Department of Biology, University of Copenhagen, Copenhagen, Denmark; Structural Biophysics, Niels Bohr Institute, Faculty of Science, University of Copenhagen, Copenhagen, Denmark.
          [2 ] Structural Biology and NMR Laboratory & Linderstrøm-Lang Centre for Protein Science, Department of Biology, University of Copenhagen, Copenhagen, Denmark; Atomistic Simulations Laboratory, Istituto Italiano di Tecnologia, Genova, Italy.
          [3 ] Structural Biology and NMR Laboratory & Linderstrøm-Lang Centre for Protein Science, Department of Biology, University of Copenhagen, Copenhagen, Denmark. Electronic address: lindorff@bio.ku.dk.
          Article
          S1877-1173(19)30212-1
          10.1016/bs.pmbts.2019.12.006
          32145944
          d6ad9204-bdda-458a-b9aa-c6b2d165cb06
          History

          Time-dependent,Maximum entropy,Time-resolved,Integration with experiments,Force fields,Bayesian methods,Molecular simulations

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