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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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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. |
format | Online Article Text |
id | pubmed-10324394 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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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