Bradley R J, Urry D W, Okamoto K, Rapaka R
Science. 1978 Apr 28;200(4340):435-7. doi: 10.1126/science.77040.
Succinyl derivatives of gramicidin were tested for their ability to form channels in planar artificial lipid bilayers. Both N-succinyldeformylgramicidin methyl ester and charged O-succinylgramicidin formed channels, but the channels had markedly different sizes and lifetimes. This implies that gramicidin forms channels by end-to-end association. However, the doubly charged N,O-bissuccinyldeformylgramicidin was inactive, which suggests that only end-to-end association of gramicidin may result in channel formation.
短杆菌肽的琥珀酰衍生物在平面人工脂质双分子层中形成通道的能力进行了测试。N-琥珀酰去甲酰短杆菌肽甲酯和带电荷的O-琥珀酰短杆菌肽均能形成通道,但这些通道的大小和寿命明显不同。这意味着短杆菌肽通过端对端缔合形成通道。然而,双电荷的N,O-双琥珀酰去甲酰短杆菌肽没有活性,这表明只有短杆菌肽的端对端缔合可能导致通道形成。