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Synthetic Channel-forming Peptides and Ion Selectivity

机译:合成通道形成肽和离子选择性

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摘要

Peptides made up of alternating L- and D- amino acids can form β-helices as in gramicidin A or cyclic peptides that aggregate to form tubes . In both cases the structures are hollow with all the side chains projecting outwards. Kennedy et al. postulated that peptides having the ( LLLD) _n configuration could form helices with every fourth side chain projecting inward. It is a fact that synthetic N-formyl-( LeuSerLeuGly) _6— OH, when added to a lipid bilayer, dimerizes, to form ion channels having conductances greater than that of gramicidin.
机译:由L-和D-氨基酸交替组成的肽可以像短杆菌肽A一样形成β螺旋,也可以形成形成管的环状肽。在这两种情况下,结构都是空心的,所有侧链都向外突出。肯尼迪等。假定具有(LLLD)_n构型的肽可形成螺旋,每四个侧链向内突出。事实上,当合成的N-甲酰基-(LeuSerLeuGly)_6-OH加到脂质双层中时,会发生二聚化,形成电导率大于短杆菌肽的电导率的离子通道。

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