Yu J, Abagyan R, Dong S, Gilbert A, Nussenzweig V, Tomlinson S
Department of Pathology, New York University Medical Center, New York 10016, USA.
J Exp Med. 1997 Feb 17;185(4):745-53. doi: 10.1084/jem.185.4.745.
CD59 is a widely distributed membrane-bound inhibitor of the cytolytic membrane attack complex (MAC) of complement. This small (77 amino acid) glycoprotein is a member of the Ly6 superfamily of proteins and is important in protecting host cells from the lytic and proinflammatory activity of the MAC. CD59 functions by binding to C8 and/or C9 in the nascent MAC and interfering with C9 membrane insertion and polymerization. We present data obtained from a combination of molecular modeling and mutagenesis techniques, which together indicate that the active site of CD59 is located in the vicinity of a hydrophobic groove on the face of the molecule opposite to a "hydrophobic strip" suggested earlier. In addition, removal of the single N-linked glycosylation site at Asn18 of CD59 resulted in an enhancement of complement inhibitory activity.
CD59是一种广泛分布的膜结合蛋白,可抑制补体的溶细胞性膜攻击复合物(MAC)。这种小的(77个氨基酸)糖蛋白是Ly6蛋白质超家族的成员,在保护宿主细胞免受MAC的溶解和促炎活性方面很重要。CD59通过与新生MAC中的C8和/或C9结合并干扰C9的膜插入和聚合来发挥作用。我们展示了从分子建模和诱变技术相结合中获得的数据,这些数据共同表明CD59的活性位点位于分子表面与先前提出的“疏水带”相对的疏水凹槽附近。此外,去除CD59第18位天冬酰胺处的单个N-连接糖基化位点会增强补体抑制活性。