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Recombinant expression a novel fibronectin—collage fusion peptide modulating stem cell stemness via integrin β3

ABSTRACT: Constructing bionic extracellular matrix (ECM) is an attractive proposition for tissue engineering and clinical regeneration therapy involving the stemness of stem cells. Here, a novel recombinant protein fibronectin-collagen peptide (FCP) was designed to modulate the function of ECM expre...

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Autores principales: Luo, Xin, Geng, Dezhi, Zhang, Qirong, Ye, Tao, Zhang, Yifan, Li, Ziyi, Huang, Yadong, Xiang, Qi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9151557/
https://www.ncbi.nlm.nih.gov/pubmed/35590080
http://dx.doi.org/10.1007/s00253-022-11965-4
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author Luo, Xin
Geng, Dezhi
Zhang, Qirong
Ye, Tao
Zhang, Yifan
Li, Ziyi
Huang, Yadong
Xiang, Qi
author_facet Luo, Xin
Geng, Dezhi
Zhang, Qirong
Ye, Tao
Zhang, Yifan
Li, Ziyi
Huang, Yadong
Xiang, Qi
author_sort Luo, Xin
collection PubMed
description ABSTRACT: Constructing bionic extracellular matrix (ECM) is an attractive proposition for tissue engineering and clinical regeneration therapy involving the stemness of stem cells. Here, a novel recombinant protein fibronectin-collagen peptide (FCP) was designed to modulate the function of ECM expressed by Picha. pastoris strain X33. This FCP promotes cell migration and adhesion and maintains rBMSC stemness by binding integrin β3. Its effects were blocked by both integrin β3 siRNA and the integrin β3 inhibitor Cilengitide. A template-independent ab initio prediction modeling approach is the best approach to construct a stable FCP protein model, which predicts the binding sites between FCP and integrin β3. FCP may be used in the in vitro culture and clinical regeneration of stem cells that highly express integrin β3, such as hematopoietic stem cells. The study provides information on the molecular structure of FCP and its bioactivity, which can be used to design new compounds. KEY POINTS: • Design a novel recombinant fibronectin-collagen peptide biomimetic ECM. • FCP promotes cell adhesion, migration, and proliferation. • Predicted and verified FCP structure and affinity with integrin β3. • FCP binds integrin β3 to maintain rBMSC stemness. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00253-022-11965-4.
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spelling pubmed-91515572022-06-01 Recombinant expression a novel fibronectin—collage fusion peptide modulating stem cell stemness via integrin β3 Luo, Xin Geng, Dezhi Zhang, Qirong Ye, Tao Zhang, Yifan Li, Ziyi Huang, Yadong Xiang, Qi Appl Microbiol Biotechnol Methods and Protocols ABSTRACT: Constructing bionic extracellular matrix (ECM) is an attractive proposition for tissue engineering and clinical regeneration therapy involving the stemness of stem cells. Here, a novel recombinant protein fibronectin-collagen peptide (FCP) was designed to modulate the function of ECM expressed by Picha. pastoris strain X33. This FCP promotes cell migration and adhesion and maintains rBMSC stemness by binding integrin β3. Its effects were blocked by both integrin β3 siRNA and the integrin β3 inhibitor Cilengitide. A template-independent ab initio prediction modeling approach is the best approach to construct a stable FCP protein model, which predicts the binding sites between FCP and integrin β3. FCP may be used in the in vitro culture and clinical regeneration of stem cells that highly express integrin β3, such as hematopoietic stem cells. The study provides information on the molecular structure of FCP and its bioactivity, which can be used to design new compounds. KEY POINTS: • Design a novel recombinant fibronectin-collagen peptide biomimetic ECM. • FCP promotes cell adhesion, migration, and proliferation. • Predicted and verified FCP structure and affinity with integrin β3. • FCP binds integrin β3 to maintain rBMSC stemness. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00253-022-11965-4. Springer Berlin Heidelberg 2022-05-20 2022 /pmc/articles/PMC9151557/ /pubmed/35590080 http://dx.doi.org/10.1007/s00253-022-11965-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Methods and Protocols
Luo, Xin
Geng, Dezhi
Zhang, Qirong
Ye, Tao
Zhang, Yifan
Li, Ziyi
Huang, Yadong
Xiang, Qi
Recombinant expression a novel fibronectin—collage fusion peptide modulating stem cell stemness via integrin β3
title Recombinant expression a novel fibronectin—collage fusion peptide modulating stem cell stemness via integrin β3
title_full Recombinant expression a novel fibronectin—collage fusion peptide modulating stem cell stemness via integrin β3
title_fullStr Recombinant expression a novel fibronectin—collage fusion peptide modulating stem cell stemness via integrin β3
title_full_unstemmed Recombinant expression a novel fibronectin—collage fusion peptide modulating stem cell stemness via integrin β3
title_short Recombinant expression a novel fibronectin—collage fusion peptide modulating stem cell stemness via integrin β3
title_sort recombinant expression a novel fibronectin—collage fusion peptide modulating stem cell stemness via integrin β3
topic Methods and Protocols
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9151557/
https://www.ncbi.nlm.nih.gov/pubmed/35590080
http://dx.doi.org/10.1007/s00253-022-11965-4
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