2XTJ
The crystal structure of PCSK9 in complex with 1D05 Fab
2XTJ の概要
エントリーDOI | 10.2210/pdb2xtj/pdb |
関連するPDBエントリー | 2W2M 2W2N 2W2O 2W2P 2W2Q |
分子名称 | PROPROTEIN CONVERTASE SUBTILISIN/KEXIN TYPE 9, FAB FROM A HUMAN MONOCLONAL ANTIBODY, 1D05, PROPROTEIN CONVERTASE SUBTILISIN-KEXIN TYPE 9, ... (8 entities in total) |
機能のキーワード | hydrolase-antibody complex, serine protease, ldl-c, ldlr, egf-a, hypercholesterolemia, hydrolase/antibody |
由来する生物種 | HOMO SAPIENS (HUMAN) 詳細 |
タンパク質・核酸の鎖数 | 6 |
化学式量合計 | 96433.25 |
構造登録者 | |
主引用文献 | Ni, Y.G.,Di Marco, S.,Condra, J.H.,Peterson, L.B.,Wang, W.,Wang, F.,Pandit, S.,Hammond, H.A.,Rosa, R.,Cummings, R.T.,Wood, D.D.,Liu, X.,Bottomley, M.J.,Shen, X.,Cubbon, R.M.,Wang, S.P.,Johns, D.G.,Volpari, C.,Hamuro, L.,Chin, J.,Huang, L.,Zhao, J.Z.,Vitelli, S.,Haytko, P.,Wisniewski, D.,Mitnaul, L.J.,Sparrow, C.P.,Hubbard, B.,Carfi, A.,Sitlani, A. A Pcsk9-Binding Antibody that Structurally Mimics the Egf(A) Domain of Ldl-Receptor Reduces Ldl Cholesterol in Vivo. J.Lipid Res., 52:78-, 2011 Cited by PubMed Abstract: Proprotein convertase subtilisin-like/kexin type 9 (PCSK9) regulates LDL cholesterol levels by inhibiting LDL receptor (LDLr)-mediated cellular LDL uptake. We have identified a fragment antigen-binding (Fab) 1D05 which binds PCSK9 with nanomolar affinity. The fully human antibody 1D05-IgG2 completely blocks the inhibitory effects of wild-type PCSK9 and two gain-of-function human PCSK9 mutants, S127R and D374Y. The crystal structure of 1D05-Fab bound to PCSK9 reveals that 1D05-Fab binds to an epitope on the PCSK9 catalytic domain which includes the entire LDLr EGF(A) binding site. Notably, the 1D05-Fab CDR-H3 and CDR-H2 loops structurally mimic the EGF(A) domain of LDLr. In a transgenic mouse model (CETP/LDLr-hemi), in which plasma lipid and PCSK9 profiles are comparable to those of humans, 1D05-IgG2 reduces plasma LDL cholesterol to 40% and raises hepatic LDLr protein levels approximately fivefold. Similarly, in healthy rhesus monkeys, 1D05-IgG2 effectively reduced LDL cholesterol 20%-50% for over 2 weeks, despite its relatively short terminal half-life (t(1/2) = 3.2 days). Importantly, the decrease in circulating LDL cholesterol corresponds closely to the reduction in free PCSK9 levels. Together these results clearly demonstrate that the LDL-lowering effect of the neutralizing anti-PCSK9 1D05-IgG2 antibody is mediated by reducing the amount of PCSK9 that can bind to the LDLr. PubMed: 20959675DOI: 10.1194/JLR.M011445 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.7 Å) |
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