Latorre R, Miller C G, Quay S
Biophys J. 1981 Dec;36(3):803-9. doi: 10.1016/S0006-3495(81)84767-4.
Alamethicin, a linear 20-amino acid antibiotic, forms voltage-dependent channels in lipid bilayer membranes. We show here that alamethicin-phospholipid conjugates can be prepared by photolysis of unilamellar vesicles containing alamethicin and a phosphatidylcholine analogue with a carbene precursor at the end of the C-2 fatty acyl chain. This result indicates that at least a portion of the alamethicin molecule is in contact with the hydrocarbon moiety of the membrane in the absence of an applied voltage. Furthermore, the alamethicin-phospholipid photoproduct is able to induce a voltage-gated conductance similar to that of natural alamethicin. The importance of these results in terms of mechanisms for channel gating is discussed.
短杆菌肽A是一种由20个氨基酸组成的线性抗生素,可在脂质双分子层膜中形成电压依赖性通道。我们在此表明,短杆菌肽A - 磷脂共轭物可通过光解含有短杆菌肽A和一种在C - 2脂肪酰链末端带有卡宾前体的磷脂酰胆碱类似物的单层囊泡来制备。这一结果表明,在没有施加电压的情况下,短杆菌肽A分子的至少一部分与膜的烃基部分接触。此外,短杆菌肽A - 磷脂光产物能够诱导出与天然短杆菌肽A类似的电压门控电导。本文讨论了这些结果在通道门控机制方面的重要性。