UdR INSTM, Department of Pharmaceutical Sciences, University of Pisa, Via Bonanno 6, 56126 Pisa, Italy; E-Mail:
Int J Mol Sci. 2010 Oct 11;11(10):3867-84. doi: 10.3390/ijms11103867.
The work presented here is aimed at suggesting plausible hypotheses for functional oligomeric forms of the human asialoglycoprotein receptor (ASGP-R), by applying a combination of different computational techniques. The functional ASGP-R is a hetero-oligomer, that comprises of several subunits of two different kinds (H1 and H2), which are highly homologous. Its stoichiometry is still unknown. An articulated step-wise modeling protocol was used in order to build the receptor model in a minimal oligomeric form, necessary for it to bind multi-antennary carbohydrate ligands. The ultimate target of the study is to contribute to increasing the knowledge of interactions between the human ASGP-R and carbohydrate ligands, at the molecular level, pertinent to applications in the field of hepatic tissue engineering.
本工作旨在通过应用多种计算技术的组合,为人类去唾液酸糖蛋白受体(ASGP-R)的功能寡聚形式提出合理的假设。功能性 ASGP-R 是一种异源寡聚体,由两种不同类型(H1 和 H2)的几个亚基组成,它们具有高度同源性。其化学计量仍未知。为了构建受体模型以形成最小的寡聚形式,从而使其能够结合多天线碳水化合物配体,使用了一种有条理的逐步建模方案。该研究的最终目标是有助于增加对人类 ASGP-R 与碳水化合物配体之间相互作用的认识,从分子水平上提高肝组织工程领域的应用水平。