Acetyl-Terminated and Template-Assembled Collagen-Based Polypeptides Composed of Gly-Pro-Hyp Sequences. 2. Synthesis and Conformational Analysis by Circular Dichroism, Ultraviolet Absorbance, and Optical Rotation
作者:Yangbo Feng、Giuseppe Melacini、Joseph P. Taulane、Murray Goodman
DOI:10.1021/ja961260c
日期:1996.1.1
absorbance, optical rotation, and nuclear magnetic resonance measurements. The acetyl analogs, Ac-(Gly-Pro-Hyp)n-NH2 (n = 6, 9), assume a stable triple-helical conformation in H2O (0.2 mg/mL) at room temperature. By contrast, Ac-(Gly-Pro-Hyp)5-NH2 adopts a triple-helical conformation in H2O only below 18 °C at a concentration of 0.2 mg/mL. For the template-assembled collagen analogs, results show that KTA-[
模板组装的基于胶原蛋白的多肽 KTA-[Gly-(Gly-Pro-Hyp)n-NH2]3 (n = 1, 3, 5, 6; KTA 是 cis,cis-1,3,5-trimethylcyclogeneration-1 ,3,5-三羧酸,也称为 Kemp 三酸)和乙酰端基单链胶原基类似物 Ac-(Gly-Pro-Hyp)n-NH2(n = 1, 3, 5, 6, 9 ) 是通过固相段缩合方法合成的。使用圆二色性、紫外吸收、旋光度和核磁共振测量研究了这些胶原类似物的三螺旋倾向。乙酰基类似物 Ac-(Gly-Pro-Hyp)n-NH2 (n = 6, 9) 在室温下在 H2O (0.2 mg/mL) 中呈现稳定的三螺旋构象。相比之下,Ac-(Gly-Pro-Hyp)5-NH2 在 H2O 中仅在 18 °C 以下,浓度为 0.2 mg/mL 时采用三螺旋构象。对于模板组装的胶原类似物,结果表明,