Studying in vitro membrane curvature recognition by proteins and its role in vesicular trafficking
| hal.structure.identifier | Compartimentation et dynamique cellulaires [CDC] | |
| dc.contributor.author | MANNEVILLE, Jean-Baptiste | |
| hal.structure.identifier | lp2n-04,lp2n-12 | |
| dc.contributor.author | LEDUC, Cecile | |
| hal.structure.identifier | Physico-Chimie-Curie [PCC] | |
| dc.contributor.author | SORRE, Benoît | |
| hal.structure.identifier | Institut de pharmacologie moléculaire et cellulaire [IPMC] | |
| dc.contributor.author | DRIN, Guillaume | |
| dc.date.accessioned | 2023-05-12T10:25:00Z | |
| dc.date.available | 2023-05-12T10:25:00Z | |
| dc.date.created | 2011-07-01 | |
| dc.date.issued | 2012-03-01 | |
| dc.identifier.issn | 0091-679X | |
| dc.identifier.uri | https://oskar-bordeaux.fr/handle/20.500.12278/181233 | |
| dc.description.abstractEn | In recent years, the interest for proteins that exert key functions in vesicular trafficking through their ability to sense or induce positive membrane curvature has expanded. In this chapter, we first present simple protocols to determine whether a protein targets positively curved membranes with liposomes of well-defined size. Next we describe more sophisticated approaches based on the controlled deformation of giant liposomes. These approaches allow visualization and quantification of protein binding to membrane regions of high curvature by real-time fluorescence microscopy. Last we describe several functional assays to measure how membrane curvature controls the activation state of Arf1 via ArfGAP1 or the asymmetric tethering between flat and curved membranes via the golgin GMAP-210. | |
| dc.language.iso | en | |
| dc.publisher | Elsevier | |
| dc.title.en | Studying in vitro membrane curvature recognition by proteins and its role in vesicular trafficking | |
| dc.type | Article de revue | |
| dc.identifier.doi | 10.1016/B978-0-12-386487-1.00003-1 | |
| dc.subject.hal | Physique [physics]/Physique [physics]/Biophysique [physics.bio-ph] | |
| bordeaux.journal | Methods in Cell Biology | |
| bordeaux.page | 47 | |
| bordeaux.volume | 108 | |
| bordeaux.hal.laboratories | Laboratoire Photonique, Numérique et Nanosciences (LP2N) - UMR 5298 | * |
| bordeaux.institution | Université de Bordeaux | |
| bordeaux.institution | CNRS | |
| bordeaux.peerReviewed | oui | |
| hal.identifier | hal-00759930 | |
| hal.version | 1 | |
| hal.origin.link | https://hal.archives-ouvertes.fr//hal-00759930v1 | |
| bordeaux.COinS | ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Methods%20in%20Cell%20Biology&rft.date=2012-03-01&rft.volume=108&rft.spage=47&rft.epage=47&rft.eissn=0091-679X&rft.issn=0091-679X&rft.au=MANNEVILLE,%20Jean-Baptiste&LEDUC,%20Cecile&SORRE,%20Beno%C3%AEt&DRIN,%20Guillaume&rft.genre=article |
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