Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1945335 | Biochimica et Biophysica Acta (BBA) - Biomembranes | 2007 | 9 Pages |
Abstract
Considerable progress has been made recently on solution NMR studies of multi-transmembrane helix membrane protein systems of increasing size. Careful correlation of structure with function has validated the physiological relevance of these studies in detergent micelles. However, larger micelle and bicelle systems are sometimes required to stabilize the active forms of dynamic membrane proteins, such as the bacterial small multidrug resistance transporters. Even in these systems with aggregate molecular weights well over 100 kDa, solution NMR structural studies are feasible—but challenging.
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Authors
Sébastien F. Poget, Mark E. Girvin,