Pardi A, Zhang X L, Selsted M E, Skalicky J J, Yip P F
Department of Chemistry and Biochemistry, University of Colorado, Boulder 80309-0215.
Biochemistry. 1992 Nov 24;31(46):11357-64. doi: 10.1021/bi00161a013.
The solution structure of two homologous naturally occurring antimicrobial peptides, rabbit defensin NP-2 and human defensin HNP-1, have been determined by two-dimensional nuclear magnetic resonance spectroscopy, distance geometry, and restrained molecular dynamics calculations. The structure of these defensins consists of an antiparallel beta-sheet in a hairpin conformation, a short region of triple-stranded beta-sheet, several tight turns, and a loop region that has a well-defined local structure but with a global orientation that is not well-defined with respect to the rest of the molecule. The solution structures of these two peptides are compared with the solution and crystal structures of two other homologous defensins. The structures for the defensins are also compared with known structures of other naturally occurring antimicrobial peptides.
通过二维核磁共振光谱、距离几何和受限分子动力学计算,确定了两种同源天然存在的抗菌肽——兔防御素NP-2和人防御素HNP-1的溶液结构。这些防御素的结构由呈发夹构象的反平行β-折叠、短的三链β-折叠区域、几个紧密转角以及一个具有明确局部结构但相对于分子其余部分全局取向不明确的环区域组成。将这两种肽的溶液结构与另外两种同源防御素的溶液结构和晶体结构进行了比较。还将防御素的结构与其他天然存在的抗菌肽的已知结构进行了比较。