Fragment-Based Discovery of an Apolipoprotein E4 (apoE4) Stabilizer

被引:22
作者
Petros, Andrew M. [1 ]
Korepanova, Alla [1 ]
Jakob, Clarissa G. [1 ]
Qiu, Wei [1 ]
Panchal, Sanjay C. [1 ]
Wang, Jie [1 ]
Dietrich, Justin D. [1 ]
Brewer, Jason T. [1 ]
Pohlki, Frauke [2 ]
Kling, Andreas [2 ]
Wilcox, Kyle [1 ]
Lakics, Viktor [2 ]
Bahnassawy, Lamiaa [2 ]
Reinhardt, Peter [2 ]
Partha, Sarathy Karunan [1 ]
Bodelle, Pierre M. [1 ]
Lake, Marc [1 ]
Charych, Erik I. [3 ]
Stoll, Vincent S. [1 ]
Sun, Chaohong [1 ]
Mohler, Eric G. [1 ]
机构
[1] AbbVie, Res & Dev, 1 North Waukegan Rd, N Chicago, IL 60064 USA
[2] AbbVie Deutschland GmbH & Co KG, Neurosci Res, Knollstr, D-67061 Ludwigshafen, Germany
[3] AbbVie Neurosci Res, 200 Sydney St, Cambridge, MA 02139 USA
关键词
ALZHEIMER-DISEASE; MOUSE MODEL; CONVERSION; RISK;
D O I
10.1021/acs.jmedchem.9b00178
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Apolipoprotein E is a 299-residue lipid carrier protein produced in both the liver and the brain. The protein has three major isoforms denoted apoE2, apoE3, and apoE4 which differ at positions 112 and 158 and which occur at different frequencies in the human population. Genome-wide association studies indicate that the possession of two apoE4 alleles is a strong genetic risk factor for late-onset Alzheimer's disease (LOAD). In an attempt to identify a small molecule stabilizer of apoE4 function that may have utility as a therapy for Alzheimer's disease, we carried out an NMR-based fragment screen on the N-terminal domain of apoE4 and identified a benzyl amidine based fragment binder. In addition to NMR, binding was characterized using various other biophysical techniques, and a crystal structure of the bound core was obtained. Core elaboration ultimately yielded a compound that showed activity in an IL-6 and IL-8 cytokine release assay.
引用
收藏
页码:4120 / 4130
页数:11
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