Duncan R, Cable H C, Rypácek F, Drobník J, Lloyd J B
Biochim Biophys Acta. 1985 Jun 18;840(2):291-3. doi: 10.1016/0304-4165(85)90131-x.
Previously it has been shown (Duncan, R., Starling, D., Rypácek, F., Drobník, J. and Lloyd, J.B. (1982) Biochim. Biophys. Acta 717, 248-254) that incorporation of tyramine residues into poly (alpha, beta-(N-2-hydroxyethyl]-DL-aspartamide (PHEA) greatly increases its rate of pinocytic uptake by rat visceral yolk sacs cultured in vitro. Here we describe the relationship between the tyramine content (1.2-21.9 mol%) of modified PHEA and its rate of uptake by yolk sacs. Above a level of substitution of approximately 10 mol% the rate of uptake rises rapidly, and the concentration-dependence of capture is indicative of uptake by adsorptive pinocytosis. Serum proteins were shown to compete effectively for membrane binding sites, indicating a nonspecific interaction of PHEA-derivatives with the yolk sac membrane. PHEA derivatives of the same tyramine content, but of different mean molecular weights (Mr), were captured at the same rates.
此前已有研究表明(邓肯,R.,斯塔林,D.,里帕切克,F.,德罗布尼克,J.和劳埃德,J.B.(1982年)《生物化学与生物物理学报》717卷,248 - 254页),将酪胺残基引入聚(α,β -(N - 2 - 羟乙基)- DL - 天冬酰胺(PHEA)中,可显著提高其被体外培养的大鼠内脏卵黄囊胞饮摄取的速率。在此,我们描述了修饰后的PHEA中酪胺含量(1.2 - 21.9摩尔%)与其被卵黄囊摄取速率之间的关系。当取代水平高于约10摩尔%时,摄取速率迅速上升,且摄取的浓度依赖性表明其通过吸附性胞饮作用摄取。血清蛋白被证明能有效竞争膜结合位点,这表明PHEA衍生物与卵黄囊膜存在非特异性相互作用。酪胺含量相同但平均分子量(Mr)不同的PHEA衍生物,其摄取速率相同。