4.7 Article

Optimization of non-equilibrium self-assembly protocols using Markov state models

期刊

JOURNAL OF CHEMICAL PHYSICS
卷 157, 期 24, 页码 -

出版社

AIP Publishing
DOI: 10.1063/5.0130407

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资金

  1. Brandeis NSF MRSEC, Bioinspired Soft Materials [DMR-2011846]
  2. NSF [TG-MCB090163, DMR-MRSEC 2011846, OAC-1920147]
  3. [NIH R01GM108021]

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The promise of self-assembly to enable the formation of materials with desired structures has driven efforts to uncover rational design principles. However, ensuring the accessibility of the target structure remains a challenge. In this study, the authors develop a framework combining Markov state model analysis with optimal control theory to optimize self-assembly protocols and maximize the yield of the target structure.
The promise of self-assembly to enable the bottom-up formation of materials with prescribed architectures and functions has driven intensive efforts to uncover rational design principles for maximizing the yield of a target structure. Yet, despite many successful examples of self-assembly, ensuring kinetic accessibility of the target structure remains an unsolved problem in many systems. In particular, long-lived kinetic traps can result in assembly times that vastly exceed experimentally accessible timescales. One proposed solution is to design non-equilibrium assembly protocols in which system parameters change over time to avoid such kinetic traps. Here, we develop a framework to combine Markov state model (MSM) analysis with optimal control theory to compute a time-dependent protocol that maximizes the yield of the target structure at a finite time. We present an adjoint-based gradient descent method that, in conjunction with MSMs for a system as a function of its control parameters, enables efficiently optimizing the assembly protocol. We also describe an interpolation approach to significantly reduce the number of simulations required to construct the MSMs. We demonstrate our approach with two examples; a simple semi-analytic model for the folding of a polymer of colloidal particles, and a more complex model for capsid assembly. Our results show that optimizing time-dependent protocols can achieve significant improvements in the yields of selected structures, including equilibrium free energy minima, long-lived metastable structures, and transient states. Published under an exclusive license by AIP Publishing.

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