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Affinity Purificati...
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Lundgren, Anders,1978Universität für Bodenkultur,University of Natural Resources and Life Sciences,Chalmers tekniska högskola,Chalmers University of Technology
(författare)
Affinity Purification and Single-Molecule Analysis of Integral Membrane Proteins from Crude Cell-Membrane Preparations
- Artikel/kapitelEngelska2018
Förlag, utgivningsår, omfång ...
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2017-12-21
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American Chemical Society (ACS),2018
Nummerbeteckningar
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LIBRIS-ID:oai:research.chalmers.se:80a4782e-7afb-4cf4-a101-84cd2ce44f35
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https://doi.org/10.1021/acs.nanolett.7b04227DOI
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https://research.chalmers.se/publication/504998URI
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https://research.chalmers.se/publication/500067URI
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Språk:engelska
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Sammanfattning på:engelska
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Ämneskategori:art swepub-publicationtype
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Ämneskategori:ref swepub-contenttype
Anmärkningar
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The function of integral membrane proteins is critically dependent on their naturally surrounding lipid membrane. Detergent-solubilized and purified membrane proteins are therefore often reconstituted into cell-membrane mimics and analyzed for their function with single-molecule microscopy. Expansion of this approach toward a broad range of pharmaceutically interesting drug targets and biomarkers however remains hampered by the fact that these proteins have low expression levels, and that detergent solubilization and reconstitution often cause protein conformational changes and loss of membrane-specific cofactors, which may impair protein function. To overcome this limitation, we here demonstrate how antibody-modified nanoparticles can be used to achieve affinity purification and enrichment of selected integral membrane proteins directly from cell membrane preparations. Nanoparticles were first bound to the ectodomain of β-secretase 1 (BACE1) contained in cell-derived membrane vesicles. In a subsequent step, these were merged into a continuous supported membrane in a microfluidic channel. Through the extended nanoparticle tag, a weak (∼fN) hydrodynamic force could be applied, inducing directed in-membrane movement of targeted BACE1 exclusively. This enabled selective thousand-fold enrichment of the targeted membrane protein while preserving a natural lipid environment. In addition, nanoparticle-targeting also enabled simultaneous tracking analysis of each individual manipulated protein, revealing how their mobility changed when moved from one lipid environment to another. We therefore believe this approach will be particularly useful for separation in-line with single-molecule analysis, eventually opening up for membrane-protein sorting devices analogous to fluorescence-activated cell sorting.
Ämnesord och genrebeteckningar
Biuppslag (personer, institutioner, konferenser, titlar ...)
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Johansson Fast, Björn,1986Chalmers tekniska högskola,Chalmers University of Technology(Swepub:cth)johabj
(författare)
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Block, Stephan,1978Chalmers tekniska högskola,Chalmers University of Technology(Swepub:cth)blocks
(författare)
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Agnarsson, Björn,1977Chalmers tekniska högskola,Chalmers University of Technology(Swepub:cth)bjornag
(författare)
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Reimhult, E.Universität für Bodenkultur,University of Natural Resources and Life Sciences
(författare)
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Gunnarsson, Anders,1981AstraZeneca AB(Swepub:cth)kb01guan
(författare)
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Höök, Fredrik,1966Chalmers tekniska högskola,Chalmers University of Technology(Swepub:cth)fredrikh
(författare)
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Universität für BodenkulturChalmers tekniska högskola
(creator_code:org_t)
Sammanhörande titlar
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Ingår i:Nano Letters: American Chemical Society (ACS)18:1, s. 381-3851530-69921530-6984
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