Becerra S P
Laboratory of Retinal Cell and Molecular Biology, National Eye Institute, National Institutes of Health, Bethesda, Maryland 20892-2740, USA.
Adv Exp Med Biol. 1997;425:223-37.
The neuronal differentiating and survival activities and presence of PEDF next to the neural retina support the idea that this serpin plays a neurotrophic role in vivo. The knowledge of the PEDF structure has provided information on the determinants for the noninhibitory and neurotrophic activities. PEDF has characteristics of a substrate rather than an inhibitor of serine proteases. Further studies are needed to identify the missing structural elements on PEDF that would confer serpin inhibitory activity. An N-terminus peptide region provides the neurotrophic function to the PEDF protein while other structural characteristics are dispensable (e.g. signal peptide, oligosaccharides on the polypeptide backbone, serpin exposed loop). During evolution PEDF might have lost its inhibitory activity and gained its neurotrophic function. Particular activities on other serpins have been reported (e.g. angiotensinogen, maspin, etc.). PEDF is an example of the separation of inhibitory and particular activities in a serpin.
神经元分化和存活活性以及神经视网膜旁存在的PEDF支持了这种丝氨酸蛋白酶抑制剂在体内发挥神经营养作用的观点。PEDF结构的知识为非抑制性和神经营养活性的决定因素提供了信息。PEDF具有丝氨酸蛋白酶底物而非抑制剂的特征。需要进一步研究来确定PEDF上赋予丝氨酸蛋白酶抑制剂活性的缺失结构元件。N端肽区域赋予PEDF蛋白神经营养功能,而其他结构特征则是可有可无的(例如信号肽、多肽主链上的寡糖、丝氨酸蛋白酶抑制剂暴露环)。在进化过程中,PEDF可能失去了其抑制活性并获得了神经营养功能。已报道了对其他丝氨酸蛋白酶抑制剂的特殊活性(例如血管紧张素原、maspin等)。PEDF是丝氨酸蛋白酶抑制剂中抑制活性和特殊活性分离的一个例子。