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Microcompartmentalization Controls Silk Feedstock Rheology

[Image: see text] The rheological characteristics of pre-spun native silk protein, which is stored as a viscous pulp inside the silk gland, are the key factors that determine the mechanical performance of the endpoint material: the spun silk fibers. In silkworms and arthropods, microcompartmentaliza...

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Autores principales: Miali, Marco Elvino, Eliaz, Dror, Solomonov, Aleksei, Shimanovich, Ulyana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10324394/
https://www.ncbi.nlm.nih.gov/pubmed/37343062
http://dx.doi.org/10.1021/acs.langmuir.3c00354
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author Miali, Marco Elvino
Eliaz, Dror
Solomonov, Aleksei
Shimanovich, Ulyana
author_facet Miali, Marco Elvino
Eliaz, Dror
Solomonov, Aleksei
Shimanovich, Ulyana
author_sort Miali, Marco Elvino
collection PubMed
description [Image: see text] The rheological characteristics of pre-spun native silk protein, which is stored as a viscous pulp inside the silk gland, are the key factors that determine the mechanical performance of the endpoint material: the spun silk fibers. In silkworms and arthropods, microcompartmentalization was shown to play an important regulatory role in storing and stabilizing the aggregation-prone silk and in initiating the fibrillar self-assembly process. However, our current understanding of the mechanism of stabilization of the highly unstable protein pulp in its soluble state inside the microcompartments and of the conditions required for initiating the structural transition in protein inside the microcompartments remains limited. Here, we exploited the power of droplet microfluidics to mimic the silk protein’s microcompartmentalization event; we introduced changes in the chemical environment and analyzed the storage-to-spinning transition as well as the accompanying structural changes in silk fibroin protein, from its native fold into an aggregative β-sheet-rich structure. Through a combination of experimental and computational simulations, we established the conditions under which the structural transition in microcompartmentalized silk protein is initiated, which, in turn, is reflected in changes in the silk-rich fluid behavior. Overall, our study sheds light on the role of the independent parameters of a dynamically changing chemical environment, changes in fluid viscosity, and the shear forces that act to balance silk protein self-assembly, and thus, facilitate new exploratory avenues in the field of biomaterials.
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spelling pubmed-103243942023-07-07 Microcompartmentalization Controls Silk Feedstock Rheology Miali, Marco Elvino Eliaz, Dror Solomonov, Aleksei Shimanovich, Ulyana Langmuir [Image: see text] The rheological characteristics of pre-spun native silk protein, which is stored as a viscous pulp inside the silk gland, are the key factors that determine the mechanical performance of the endpoint material: the spun silk fibers. In silkworms and arthropods, microcompartmentalization was shown to play an important regulatory role in storing and stabilizing the aggregation-prone silk and in initiating the fibrillar self-assembly process. However, our current understanding of the mechanism of stabilization of the highly unstable protein pulp in its soluble state inside the microcompartments and of the conditions required for initiating the structural transition in protein inside the microcompartments remains limited. Here, we exploited the power of droplet microfluidics to mimic the silk protein’s microcompartmentalization event; we introduced changes in the chemical environment and analyzed the storage-to-spinning transition as well as the accompanying structural changes in silk fibroin protein, from its native fold into an aggregative β-sheet-rich structure. Through a combination of experimental and computational simulations, we established the conditions under which the structural transition in microcompartmentalized silk protein is initiated, which, in turn, is reflected in changes in the silk-rich fluid behavior. Overall, our study sheds light on the role of the independent parameters of a dynamically changing chemical environment, changes in fluid viscosity, and the shear forces that act to balance silk protein self-assembly, and thus, facilitate new exploratory avenues in the field of biomaterials. American Chemical Society 2023-06-21 /pmc/articles/PMC10324394/ /pubmed/37343062 http://dx.doi.org/10.1021/acs.langmuir.3c00354 Text en © 2023 American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Miali, Marco Elvino
Eliaz, Dror
Solomonov, Aleksei
Shimanovich, Ulyana
Microcompartmentalization Controls Silk Feedstock Rheology
title Microcompartmentalization Controls Silk Feedstock Rheology
title_full Microcompartmentalization Controls Silk Feedstock Rheology
title_fullStr Microcompartmentalization Controls Silk Feedstock Rheology
title_full_unstemmed Microcompartmentalization Controls Silk Feedstock Rheology
title_short Microcompartmentalization Controls Silk Feedstock Rheology
title_sort microcompartmentalization controls silk feedstock rheology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10324394/
https://www.ncbi.nlm.nih.gov/pubmed/37343062
http://dx.doi.org/10.1021/acs.langmuir.3c00354
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