Karle I L, Duesler E
Proc Natl Acad Sci U S A. 1977 Jul;74(7):2602-6. doi: 10.1073/pnas.74.7.2602.
The synthetic, biologically active, [Phe4Val6] analog of natural antamanide has been crystallized from a solution containing calcium nitrate, acetone, and acetonitrile. The crystal does not contain any Ca2+ ions but does contain 12 water molecules per peptide molecule. The conformation of this dodecahydrate is identical to the trihydrate crystallized from n-hexane/methyl acetate. The packing in both crystals is very similar, governed by parallel bands of phenyl and pyrrolidine ring stacking and by continuous channels for the solvement molecules, water in this case and n-hexane/methyl acetate in the previous study. The two structures are not ideally isomorphous, since the c cell parameter differs by more than 1.0 A in the two cells. There are three functions for H2O molecules: the three intrinsic H2O molecules in the interior of the peptide ring, the H2O bound to the exposed C=O groups, and the H2O molecules that fill space in the solvent channels. There are no direct hydrogen bonds between neighboring peptide molecules and there are only two intramolecular NH-O=C bonds (of the 5 leads to 1 type).
天然抗真菌肽的合成生物活性类似物[Phe4Val6]已从含有硝酸钙、丙酮和乙腈的溶液中结晶出来。该晶体不含任何Ca2+离子,但每个肽分子含有12个水分子。这种十二水合物的构象与从正己烷/乙酸甲酯中结晶出的三水合物相同。两种晶体中的堆积方式非常相似,由苯基和吡咯烷环堆积的平行带以及溶剂分子(在这种情况下是水,在前一项研究中是正己烷/乙酸甲酯)的连续通道控制。这两种结构并非理想的同晶型,因为两个晶胞中的c晶胞参数相差超过1.0 Å。水分子有三种作用:肽环内部的三个固有水分子、与暴露的C=O基团结合的水以及填充溶剂通道空间的水分子。相邻肽分子之间没有直接的氢键,并且只有两个分子内的NH-O=C键(5个中导致1种类型)。