5MO9

Structure of human TrkB receptor ligand binding domain in complex with the Fab frgment of antibody AB20

5MO9 の概要

• エントリーDOI: 10.2210/pdb5mo9/pdb
• 分子名称: AB20 Fab heavy chain, AB20 Fab light chain, BDNF/NT-3 growth factors receptor, ... (4 entities in total)
• 機能のキーワード: trk receptor, antibody, antigen, complex, immune system
• 由来する生物種: Mus musculus (House mouse); 詳細
• タンパク質・核酸の鎖数: 3
• 化学式量合計: 64516.75

構造登録者

Hoerer, S. (登録日: 2016-12-14, 公開日: 2017-08-02, 最終更新日: 2024-01-17)

主引用文献

Traub, S.,Stahl, H.,Rosenbrock, H.,Simon, E.,Florin, L.,Hospach, L.,Horer, S.,Heilker, R.
Pharmaceutical Characterization of Tropomyosin Receptor Kinase B-Agonistic Antibodies on Human Induced Pluripotent Stem (hiPS) Cell-Derived Neurons.
J. Pharmacol. Exp. Ther., 361:355-365, 2017

PubMed Abstract: Brain-derived neurotrophic factor (BDNF) is a central modulator of neuronal development and synaptic plasticity in the central nervous system. This renders the BDNF-modulated tropomyosin receptor kinase B (TrkB) a promising drug target to treat synaptic dysfunctions. Using owth factor-driven expansion and hibition of ot (GRINCH) during maturation, the so-called GRINCH neurons were derived from human-induced pluripotent stem cells. These GRINCH neurons were used as model cells for pharmacologic profiling of two TrkB-agonistic antibodies, hereafter referred to as and In next-generation sequencing studies, AB2 and AB20 stimulated transcriptional changes, which extensively overlapped with BDNF-driven transcriptional modulation. In regard to TrkB phosphorylation, both AB2 and AB20 were only about half as efficacious as BDNF; however, with respect to the TrkB downstream signaling, AB2 and AB20 displayed increased efficacy values, providing a stimulation at least comparable to BDNF in respect to transcription, as well as of AKT and cAMP response element-binding protein phosphorylation. In a complex structure of the TrkB-d5 domain with AB20, determined by X-ray crystallography, the AB20 binding site was found to be allosteric in regard to the BDNF binding site, whereas AB2 was known to act orthosterically with BDNF. In agreement with this finding, AB2 and AB20 acted synergistically at greater concentrations to drive TrkB phosphorylation. Although TrkB downstream signaling declined faster after pulse stimulation with AB20 than with AB2, AB20 restimulated TrkB phosphorylation more efficiently than AB2. In conclusion, both antibodies displayed some limitations and some benefits in regard to future applications as therapeutic agents.

PubMed: 28351853
DOI: 10.1124/jpet.117.240184

実験手法

X-RAY DIFFRACTION (2.594 Å)