Literature DB >> 33418710

Modeling and Experiment Reveal Structure and Nanomechanics across the Inverse Temperature Transition in B. mori Silk-Elastin-like Protein Polymers.

Anna Tarakanova1, Wenwen Huang2, Zhao Qin1, David L Kaplan2, Markus J Buehler1.   

Abstract

Silk and elastin are exemplary protein materials that exhibit exceptional material properties. Silk is uniquely strong, surpassing engineering materials such as Kevlar and steel, while elastin has exquisite flexibility and can reversibly fold into a more structured form at high temperatures when many other proteins would unfold and denature. This phenomenon in elastin is termed the inverse temperature transition. It is a reversible, controllable process that motivates applications in drug delivery, shape change materials, and biomimetic devices. Silk-elastinlike protein polymers (SELPs), which combine repeating B. mori silk and elastin blocks, have been introduced as biologically inspired materials that combine the distinctive properties of the component parts to achieve strong and extensible, tunable biomaterials. Here, we considered a single SELP sequence to examine temperature transition effects at the molecular scale. SELP molecular models were created using Replica Exchange Molecular Dynamics, an accelerated sampling method, and confirmed in experiment by comparing secondary structure distributions. A molecular collapse of the SELP molecule was observed with increased temperature in both molecular simulation and experiment. Temperature-specific differences were observed in the mechanical properties and the unfolding pathways of the polypeptide. Using the Bell-Evans model, we analyzed the free energy landscape associated with molecular unfolding at temperatures below and above the transition temperature range (Tt) of the polypeptide. We found that at physiological pulling rates, the energy barrier to unfold SELPs was counterintuitively higher above Tt. Our findings offer a foundational perspective on the molecular scale mechanisms of temperature-induced phase transition in SELPs, and suggest a novel approach to combine simulation and experiment to study materials for multifunctional biomimetic applications.

Entities:  

Keywords:  B. mori silk; Bell−Evans model; elastin; inverse temperature transition; protein polymers; silk-elastinlike protein polymers (SELPs); steered molecular dynamics (SMD)

Year:  2017        PMID: 33418710      PMCID: PMC9455622          DOI: 10.1021/acsbiomaterials.6b00688

Source DB:  PubMed          Journal:  ACS Biomater Sci Eng        ISSN: 2373-9878


  47 in total

1.  GROMACS: fast, flexible, and free.

Authors:  David Van Der Spoel; Erik Lindahl; Berk Hess; Gerrit Groenhof; Alan E Mark; Herman J C Berendsen
Journal:  J Comput Chem       Date:  2005-12       Impact factor: 3.376

2.  A split ligand for lanthanide binding: facile evaluation of dimerizing proteins.

Authors:  Yue Zhao; Jianmin Gao
Journal:  Chem Commun (Camb)       Date:  2012-02-08       Impact factor: 6.222

3.  A temperature predictor for parallel tempering simulations.

Authors:  Alexandra Patriksson; David van der Spoel
Journal:  Phys Chem Chem Phys       Date:  2008-02-25       Impact factor: 3.676

4.  Structure and mechanism of maximum stability of isolated alpha-helical protein domains at a critical length scale.

Authors:  Zhao Qin; Andrea Fabre; Markus J Buehler
Journal:  Eur Phys J E Soft Matter       Date:  2013-05-29       Impact factor: 1.890

Review 5.  Entropic elastic processes in protein mechanisms. I. Elastic structure due to an inverse temperature transition and elasticity due to internal chain dynamics.

Authors:  D W Urry
Journal:  J Protein Chem       Date:  1988-02

Review 6.  Silk-elastin-like protein biomaterials for the controlled delivery of therapeutics.

Authors:  Wenwen Huang; Alexandra Rollett; David L Kaplan
Journal:  Expert Opin Drug Deliv       Date:  2014-12-05       Impact factor: 6.648

7.  Wet-spinning of recombinant silk-elastin-like protein polymer fibers with high tensile strength and high deformability.

Authors:  Weiguo Qiu; Weibing Teng; Joseph Cappello; Xiaoyi Wu
Journal:  Biomacromolecules       Date:  2009-03-09       Impact factor: 6.988

8.  Hierarchies, multiple energy barriers, and robustness govern the fracture mechanics of alpha-helical and beta-sheet protein domains.

Authors:  Theodor Ackbarow; Xuefeng Chen; Sinan Keten; Markus J Buehler
Journal:  Proc Natl Acad Sci U S A       Date:  2007-10-09       Impact factor: 11.205

9.  Silk-elastinlike recombinant polymers for gene therapy of head and neck cancer: from molecular definition to controlled gene expression.

Authors:  Joshua Gustafson; Khaled Greish; Jordan Frandsen; Joseph Cappello; Hamidreza Ghandehari
Journal:  J Control Release       Date:  2009-05-24       Impact factor: 9.776

10.  Design of Multistimuli Responsive Hydrogels Using Integrated Modeling and Genetically Engineered Silk-Elastin-Like Proteins.

Authors:  Wenwen Huang; Anna Tarakanova; Nina Dinjaski; Qin Wang; Xiaoxia Xia; Ying Chen; Joyce Y Wong; Markus J Buehler; David L Kaplan
Journal:  Adv Funct Mater       Date:  2016-04-15       Impact factor: 18.808

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  3 in total

1.  Fast and reversible crosslinking of a silk elastin-like polymer.

Authors:  Constancio Gonzalez-Obeso; J C Rodriguez-Cabello; David L Kaplan
Journal:  Acta Biomater       Date:  2021-12-28       Impact factor: 8.947

2.  Charge-Modulated Accessibility of Tyrosine Residues for Silk-Elastin Copolymer Cross-Linking.

Authors:  Constancio Gonzalez-Obeso; Fredrik G Backlund; David L Kaplan
Journal:  Biomacromolecules       Date:  2022-02-03       Impact factor: 6.978

Review 3.  Fibrous Scaffolds From Elastin-Based Materials.

Authors:  Jose Carlos Rodriguez-Cabello; Israel Gonzalez De Torre; Miguel González-Pérez; Fernando González-Pérez; Irene Montequi
Journal:  Front Bioeng Biotechnol       Date:  2021-07-16
  3 in total

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