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An engineered dimeric protein pore that spans adjacent lipid bilayers

The bottom-up construction of artificial tissues is an underexplored area of synthetic biology. An important challenge is communication between constituent compartments of the engineered tissue and between the engineered tissue and additional compartments, including extracellular fluids, further eng...

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Detalles Bibliográficos
Autores principales: Mantri, Shiksha, Sapra, K. Tanuj, Cheley, Stephen, Sharp, Thomas H., Bayley, Hagan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3644966/
https://www.ncbi.nlm.nih.gov/pubmed/23591892
http://dx.doi.org/10.1038/ncomms2726
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author Mantri, Shiksha
Sapra, K. Tanuj
Cheley, Stephen
Sharp, Thomas H.
Bayley, Hagan
author_facet Mantri, Shiksha
Sapra, K. Tanuj
Cheley, Stephen
Sharp, Thomas H.
Bayley, Hagan
author_sort Mantri, Shiksha
collection PubMed
description The bottom-up construction of artificial tissues is an underexplored area of synthetic biology. An important challenge is communication between constituent compartments of the engineered tissue and between the engineered tissue and additional compartments, including extracellular fluids, further engineered tissue and living cells. Here we present a dimeric transmembrane pore that can span two adjacent lipid bilayers and thereby allow aqueous compartments to communicate. Two heptameric staphylococcal α-hemolysin (αHL) pores were covalently linked in an aligned cap-to-cap orientation. The structure of the dimer, (α7)(2), was confirmed by biochemical analysis, transmission electron microscopy (TEM) and single-channel electrical recording. We show that one of two β barrels of (α7)(2) can insert into the lipid bilayer of a small unilamellar vesicle, while the other spans a planar lipid bilayer. (α7)(2) pores spanning two bilayers were also observed by TEM.
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spelling pubmed-36449662013-10-16 An engineered dimeric protein pore that spans adjacent lipid bilayers Mantri, Shiksha Sapra, K. Tanuj Cheley, Stephen Sharp, Thomas H. Bayley, Hagan Nat Commun Article The bottom-up construction of artificial tissues is an underexplored area of synthetic biology. An important challenge is communication between constituent compartments of the engineered tissue and between the engineered tissue and additional compartments, including extracellular fluids, further engineered tissue and living cells. Here we present a dimeric transmembrane pore that can span two adjacent lipid bilayers and thereby allow aqueous compartments to communicate. Two heptameric staphylococcal α-hemolysin (αHL) pores were covalently linked in an aligned cap-to-cap orientation. The structure of the dimer, (α7)(2), was confirmed by biochemical analysis, transmission electron microscopy (TEM) and single-channel electrical recording. We show that one of two β barrels of (α7)(2) can insert into the lipid bilayer of a small unilamellar vesicle, while the other spans a planar lipid bilayer. (α7)(2) pores spanning two bilayers were also observed by TEM. 2013 /pmc/articles/PMC3644966/ /pubmed/23591892 http://dx.doi.org/10.1038/ncomms2726 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Mantri, Shiksha
Sapra, K. Tanuj
Cheley, Stephen
Sharp, Thomas H.
Bayley, Hagan
An engineered dimeric protein pore that spans adjacent lipid bilayers
title An engineered dimeric protein pore that spans adjacent lipid bilayers
title_full An engineered dimeric protein pore that spans adjacent lipid bilayers
title_fullStr An engineered dimeric protein pore that spans adjacent lipid bilayers
title_full_unstemmed An engineered dimeric protein pore that spans adjacent lipid bilayers
title_short An engineered dimeric protein pore that spans adjacent lipid bilayers
title_sort engineered dimeric protein pore that spans adjacent lipid bilayers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3644966/
https://www.ncbi.nlm.nih.gov/pubmed/23591892
http://dx.doi.org/10.1038/ncomms2726
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