TY - JOUR
T1 - Electron microscopic evidence for nucleation and growth of 3D acetylcholine receptor microcrystals in structured lipid - Detergent matrices
AU - Paas, Yoav
AU - Cartaud, Jean
AU - Recouvreur, Michel
AU - Grailhe, Regis
AU - Dufresne, Virginie
AU - Pebay-Peyroula, Eva
AU - Landau, Ehud M.
AU - Changeux, Jean Pierre
PY - 2003/9/30
Y1 - 2003/9/30
N2 - Nicotinic acetylcholine receptors (AChRs) belong to a superfamily of oligomeric proteins that transduce electric signals across the cell membrane on binding of neurotransmitters. These receptors harbor a large extracellular ligand-binding domain directly linked to an ion-conducting channel-forming domain that spans the cell membrane 20 times and considerably extends into the cytoplasm. Thus far, none of these receptor channels has been crystallized in three dimensions. The crystallization of the AChR from Torpedo marmorata electric organs is challenged here in lipidic-detergent matrices. Detergent-soluble AChR complexed with β-bungarotoxin (βBTx), a polypeptidic competitive antagonist, was purified. The AChR-βBTx complex was reconstituted in a lipidic matrix composed of monoolein bilayers that are structured in three dimensions. The βBTx was conjugated to a photo-stable fluorophore, enabling us to monitor the physical behavior of the receptor-toxin complex in the lipidic matrix under light stereomicroscope, and to freeze fracture regions containing the receptor-toxin complex for visualization under a transmission electron microscope. Conditions were established for forming 2D receptor-toxin lattices that are stacked in the third dimension. 3D AChR nanocrystals were thereby grown inside the highly viscous lipidic 3D matrix. Slow emulsification of the lipidic matrix converted these nanocrystals into 3D elongated thin crystal plates of micrometer size. The latter are stable in detergent-containing aqueous solutions and can currently be used for seeding and epitaxial growth, en route to crystals of appropriate dimensions for x-ray diffraction studies.
AB - Nicotinic acetylcholine receptors (AChRs) belong to a superfamily of oligomeric proteins that transduce electric signals across the cell membrane on binding of neurotransmitters. These receptors harbor a large extracellular ligand-binding domain directly linked to an ion-conducting channel-forming domain that spans the cell membrane 20 times and considerably extends into the cytoplasm. Thus far, none of these receptor channels has been crystallized in three dimensions. The crystallization of the AChR from Torpedo marmorata electric organs is challenged here in lipidic-detergent matrices. Detergent-soluble AChR complexed with β-bungarotoxin (βBTx), a polypeptidic competitive antagonist, was purified. The AChR-βBTx complex was reconstituted in a lipidic matrix composed of monoolein bilayers that are structured in three dimensions. The βBTx was conjugated to a photo-stable fluorophore, enabling us to monitor the physical behavior of the receptor-toxin complex in the lipidic matrix under light stereomicroscope, and to freeze fracture regions containing the receptor-toxin complex for visualization under a transmission electron microscope. Conditions were established for forming 2D receptor-toxin lattices that are stacked in the third dimension. 3D AChR nanocrystals were thereby grown inside the highly viscous lipidic 3D matrix. Slow emulsification of the lipidic matrix converted these nanocrystals into 3D elongated thin crystal plates of micrometer size. The latter are stable in detergent-containing aqueous solutions and can currently be used for seeding and epitaxial growth, en route to crystals of appropriate dimensions for x-ray diffraction studies.
KW - Crystallization
KW - Nicotinic acetylcholine receptor
KW - Structure
UR - http://www.scopus.com/inward/record.url?scp=0141817680&partnerID=8YFLogxK
U2 - 10.1073/pnas.1834451100
DO - 10.1073/pnas.1834451100
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
C2 - 13679581
AN - SCOPUS:0141817680
SN - 0027-8424
VL - 100
SP - 11309
EP - 11314
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 20
ER -