Aguilar M I, Mougos S, Boublik J, Rivier J, Hearn M T
Department of Biochemistry, Monash University, Clayton, Victoria, Australia.
J Chromatogr. 1993 Aug 27;646(1):53-65. doi: 10.1016/s0021-9673(99)87007-1.
The reversed-phase high-performance liquid chromatographic (RP-HPLC) gradient elution behaviour of a series of peptides related to Neuropeptide Y (NPY) has been investigated. The peptides studied included NPY, NPY[13-36], NPY[18-36] and a series of 16 analogues of NPY[18-36], each with a single D-amino acid substitution. Chromatographic parameters which relate to the interactive contact area and the binding affinity have been evaluated with two different stationary phase ligands and two organic modifiers. The results demonstrate that D-amino acid substitutions in the sequence region encompassing amino acid residues NPY[27-31] of these NPY[18-36] peptides significantly influence the interactive behaviour of these peptides relative to the unsubstituted NPY[18-36] molecule, while substitutions in the N- and C-terminal regions had little effect. Further, these results indicate that, in hydrophobic environments, NPY[18-36] adopts a significant degree of secondary structure which is severely disrupted by the presence of the D-amino acids in the central portion of the molecule.
研究了一系列与神经肽Y(NPY)相关的肽的反相高效液相色谱(RP-HPLC)梯度洗脱行为。所研究的肽包括NPY、NPY[13-36]、NPY[18-36]以及一系列NPY[18-36]的16种类似物,每种类似物都有一个单一的D-氨基酸取代。使用两种不同的固定相配体和两种有机改性剂评估了与相互作用接触面积和结合亲和力相关的色谱参数。结果表明,这些NPY[18-36]肽中包含氨基酸残基NPY[27-31]的序列区域中的D-氨基酸取代相对于未取代的NPY[18-36]分子显著影响这些肽的相互作用行为,而N端和C端区域的取代影响很小。此外,这些结果表明,在疏水环境中,NPY[18-36]具有显著程度的二级结构,该结构因分子中部存在D-氨基酸而严重破坏。