An approach to prepare membrane proteins for single-molecule imaging
Research output: Contribution to journal › Research article › Contributed › peer-review
Contributors
Abstract
(Figure Presented) Observed from above: A cysteine mutation in a membrane protein enables it to be fixed in a defined orientation on flat gold surfaces (see picture, left). Subsequent coassembly with thiolipids produces clearly defined, immobilized proteins. Analysis by atomic force microscopy provides topographs of similar quality to those revealed from 2D crystals.
Details
Original language | English |
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Pages (from-to) | 3252-3256 |
Number of pages | 5 |
Journal | Angewandte Chemie - International Edition |
Volume | 45 |
Issue number | 20 |
Publication status | Published - 12 May 2006 |
Peer-reviewed | Yes |
External IDs
PubMed | 16634099 |
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Keywords
ASJC Scopus subject areas
Keywords
- Lipids, Membrane proteins, Porin OmpF, Protein structures, Scanning force microscopy