Summary of ssbd-repos-000125

SSBD:database
URL

Name
ssbd-repos-000125 (125-Gessesse-CX3CR1nanodisc)
URL
DOI
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Title
Transmission electron images of homogeneity of CX3CR1-nanodisc complex in a reconstituted cell-free synthesis system
Description
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Submited Date
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Release Date
2019-11-20
Updated Date
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License
Funding information
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File formats
Data size
412.7 MB

Organism
Strain
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Cell Line
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Genes
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Proteins
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GO Molecular Function (MF)
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GO Biological Process (BP)
protein transport within lipid bilayer
GO Cellular Component (CC)
membrane protein complex, G protein coupled receptor complex
Study Type
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Imaging Methods
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Method Summary
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Related paper(s)

Belay Gessesse, Takashi Nagaike, Koji Nagata, Yoshihiro Shimizu, Takuya Ueda (2018) G-Protein Coupled Receptor Protein Synthesis on a Lipid Bilayer Using a Reconstituted Cell-Free Protein Synthesis System., Life (Basel, Switzerland), Volume 8, Number 4

Published in 2018 Nov 2 (Electronic publication in Nov. 2, 2018, midnight )

(Abstract) Membrane proteins are important drug targets which play a pivotal role in various cellular activities. However, unlike cytosolic proteins, most of them are difficult-to-express proteins. In this study, to synthesize and produce sufficient quantities of membrane proteins for functional and structural analysis, we used a bottom-up approach in a reconstituted cell-free synthesis system, the PURE system, supplemented with artificial lipid mimetics or micelles. Membrane proteins were synthesized by the cell-free system and integrated into lipid bilayers co-translationally. Membrane proteins such as the G-protein coupled receptors were expressed in the PURE system and a productivity ranging from 0.04 to 0.1 mg per mL of reaction was achieved with a correct secondary structure as predicted by circular dichroism spectrum. In addition, a ligand binding constant of 27.8 nM in lipid nanodisc and 39.4 nM in micelle was obtained by surface plasmon resonance and the membrane protein localization was confirmed by confocal microscopy in giant unilamellar vesicles. We found that our method is a promising approach to study the different classes of membrane proteins in their native-like artificial lipid bilayer environment for functional and structural studies.

Contact(s)
Yoshihiro Shimizu
Organization(s)
RIKEN , Center for Biosystems Dynamics Research , Laboratory for Cell-Free Protein Synthesis
Image Data Contributors
Quantitative Data Contributors

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