Zsila Ferenc, Mády György
Chemical Research Center, Hungarian Academy of Sciences, Institute of Biomolecular Chemistry, H-1025 Budapest, Pusztaszeri út 59-67, Hungary.
Biochem Biophys Res Commun. 2008 Aug 1;372(3):503-7. doi: 10.1016/j.bbrc.2008.05.090. Epub 2008 May 27.
alpha(1)-Acid glycoprotein (AAG), an acute phase component of the human serum, is a prominent member of the lipocalin family of proteins showing inflammatory/immunomodulatory activities and promiscuous drug binding properties. Both three-dimensional structure of AAG and its precise biological function are still unknown and only a few endogenous AAG ligands have been described to date. CD spectroscopic studies performed with commercial AAG and the separated genetic variants revealed high-affinity binding of biliverdin (BV) and biliverdin dimethyl ester to the 'F1/S' fraction of the protein. The preferential accommodation of the right-handed, P-helicity conformers of the pigments by the protein matrix resulted in strong induced CD activity, which was utilized for estimation of the binding parameters and to locate the binding site. It was concluded that both pigments are bound in the central beta-barrel cavity of AAG, held principally by hydrophobic interactions. Possible biological implications of the BV binding ability of AAG with special emphasis on the heme oxygenase-1 pathway are discussed.
α(1)-酸性糖蛋白(AAG)是人类血清中的一种急性期成分,是脂质运载蛋白家族的重要成员,具有炎症/免疫调节活性和混杂的药物结合特性。AAG的三维结构及其确切的生物学功能仍然未知,迄今为止仅描述了少数内源性AAG配体。用商业AAG和分离的遗传变体进行的圆二色光谱研究表明,胆绿素(BV)和胆绿素二甲酯与该蛋白质的“F1/S”部分具有高亲和力结合。蛋白质基质对色素右手P螺旋构象异构体的优先容纳导致了强烈的诱导圆二色活性,该活性被用于估计结合参数并定位结合位点。得出的结论是,两种色素都结合在AAG的中央β桶腔中,主要通过疏水相互作用保持。讨论了AAG的BV结合能力可能的生物学意义,特别强调了血红素加氧酶-1途径。