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Self-Assembly of RGD-Functionalized Recombinant Spider Silk Protein into Microspheres in Physiological Buffer and in the Presence of Hyaluronic Acid
KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Proteinvetenskap, Proteinteknologi.ORCID-id: 0000-0002-6696-9055
KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Proteinvetenskap. Spiber Technologies AB, Roslagstullsbacken 15, 114 21 Stockholm, Sweden, Roslagstullsbacken 15.ORCID-id: 0000-0002-3654-1840
KTH, Skolan för elektroteknik och datavetenskap (EECS), Intelligenta system, Mikro- och nanosystemteknik. Spiber Technologies AB, Roslagstullsbacken 15, 114 21 Stockholm, Sweden.ORCID-id: 0000-0002-8925-2815
KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Kemi, Glykovetenskap.ORCID-id: 0000-0002-1981-3736
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2023 (engelsk)Inngår i: ACS Applied Bio Materials, E-ISSN 2576-6422, Vol. 6, nr 9, s. 3696-3705Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Biomaterials made of self-assembling protein building blocks are widely explored for biomedical applications, for example, as drug carriers, tissue engineering scaffolds, and functionalized coatings. It has previously been shown that a recombinant spider silk protein functionalized with a cell binding motif from fibronectin, FN-4RepCT (FN-silk), self-assembles into fibrillar structures at interfaces, i.e., membranes, fibers, or foams at liquid/air interfaces, and fibrillar coatings at liquid/solid interfaces. Recently, we observed that FN-silk also assembles into microspheres in the bulk of a physiological buffer (PBS) solution. Herein, we investigate the self-assembly process of FN-silk into microspheres in the bulk and how its progression is affected by the presence of hyaluronic acid (HA), both in solution and in a cross-linked HA hydrogel. Moreover, we characterize the size, morphology, mesostructure, and protein secondary structure of the FN-silk microspheres prepared in PBS and HA. Finally, we examine how the FN-silk microspheres can be used to mediate cell adhesion and spreading of human mesenchymal stem cells (hMSCs) during cell culture. These investigations contribute to our fundamental understanding of the self-assembly of silk protein into materials and demonstrate the use of silk microspheres as additives for cell culture applications.

sted, utgiver, år, opplag, sider
American Chemical Society (ACS) , 2023. Vol. 6, nr 9, s. 3696-3705
Emneord [en]
cell culture, confocal microscopy, cryo-electron microscopy, fluorescence microscopy, hyaluronic acid, recombinant spider silk, self-assembly, silk microspheres
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Identifikatorer
URN: urn:nbn:se:kth:diva-349824DOI: 10.1021/acsabm.3c00373ISI: 001048127800001PubMedID: 37579070Scopus ID: 2-s2.0-85168992000OAI: oai:DiVA.org:kth-349824DiVA, id: diva2:1881645
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QC 20240703

Tilgjengelig fra: 2024-07-03 Laget: 2024-07-03 Sist oppdatert: 2025-02-20bibliografisk kontrollert

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Ornithopoulou, EiriniÅstrand, CarolinaGustafsson, LinneaCrouzier, ThomasHedhammar, My

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