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In vitro Blood-Brain barrier model based on recombinant spider silk protein nanomembranes for evaluation of transcytosis capability of biomolecules
KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Protein Science.ORCID iD: 0000-0001-6558-0702
KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Protein Science, Protein Technology.ORCID iD: 0000-0003-0140-419X
KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Protein Science, Protein Engineering.ORCID iD: 0000-0001-9423-0541
2023 (English)In: Biochemical and Biophysical Research Communications - BBRC, ISSN 0006-291X, E-ISSN 1090-2104, Vol. 669, p. 77-84Article in journal (Refereed) Published
Abstract [en]

The blood-brain barrier (BBB) limits the uptake of central nervous system (CNS)-targeting drugs into the brain. Engineering molecular shuttles for active transportation across the barrier has thus potential for improving the efficacy of such drugs. In vitro assessment of potential transcytosis capability for engi-neered shuttle proteins facilitates ranking and the selection of promising candidates during develop-ment. Herein, the development of an assay based on brain endothelial cells cultured on permeable recombinant silk nanomembranes for screening of transcytosis capability of biomolecules is described. The silk nanomembranes supported growth of brain endothelial cells to form confluent monolayers with relevant cell morphology, and induced expression of tight-junction proteins. Evaluation of the assay using an established BBB shuttle antibody showed transcytosis over the membranes with an apparent permeability that significantly differed from the isotype control antibody.

Place, publisher, year, edition, pages
Elsevier BV , 2023. Vol. 669, p. 77-84
Keywords [en]
Blood-brain barrier, Transwell assay, Transferrin Receptor-1, Recombinant spider silk, Receptor-mediated transcytosis
National Category
Biochemistry Molecular Biology
Identifiers
URN: urn:nbn:se:kth:diva-331196DOI: 10.1016/j.bbrc.2023.05.093ISI: 001013402700001PubMedID: 37267863Scopus ID: 2-s2.0-85160288308OAI: oai:DiVA.org:kth-331196DiVA, id: diva2:1780705
Note

Not duplicate with DiVA 1740044

QC 20230706

Available from: 2023-07-06 Created: 2023-07-06 Last updated: 2026-03-17Bibliographically approved

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Hjelm, Linnea CharlottaHedhammar, MyLöfblom, John

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