6WMW

GFRAL receptor bound with two antibody Fabs (3P10, 25M22)

6WMW の概要

• エントリーDOI: 10.2210/pdb6wmw/pdb
• 分子名称: GDNF family receptor alpha-like, FAB3P10 heavy chain fragment, FAB3P10 light chain, ... (5 entities in total)
• 機能のキーワード: receptor, signaling, antibodes, immune system
• 由来する生物種: Homo sapiens (Human); 詳細
• タンパク質・核酸の鎖数: 5
• 化学式量合計: 127057.10

構造登録者

White, A.,Lakshminarasimhan, D.,Olland, A.,Suto, R.K. (登録日: 2020-04-21, 公開日: 2020-07-15, 最終更新日: 2024-10-23)

主引用文献

Suriben, R.,Chen, M.,Higbee, J.,Oeffinger, J.,Ventura, R.,Li, B.,Mondal, K.,Gao, Z.,Ayupova, D.,Taskar, P.,Li, D.,Starck, S.R.,Chen, H.H.,McEntee, M.,Katewa, S.D.,Phung, V.,Wang, M.,Kekatpure, A.,Lakshminarasimhan, D.,White, A.,Olland, A.,Haldankar, R.,Solloway, M.J.,Hsu, J.Y.,Wang, Y.,Tang, J.,Lindhout, D.A.,Allan, B.B.
Antibody-mediated inhibition of GDF15-GFRAL activity reverses cancer cachexia in mice.
Nat Med, 26:1264-1270, 2020

PubMed Abstract: Cancer cachexia is a highly prevalent condition associated with poor quality of life and reduced survival. Tumor-induced perturbations in the endocrine, immune and nervous systems drive anorexia and catabolic changes in adipose tissue and skeletal muscle, hallmarks of cancer cachexia. However, the molecular mechanisms driving cachexia remain poorly defined, and there are currently no approved drugs for the condition. Elevation in circulating growth differentiation factor 15 (GDF15) correlates with cachexia and reduced survival in patients with cancer, and a GDNF family receptor alpha like (GFRAL)-Ret proto-oncogene (RET) signaling complex in brainstem neurons that mediates GDF15-induced weight loss in mice has recently been described. Here we report a therapeutic antagonistic monoclonal antibody, 3P10, that targets GFRAL and inhibits RET signaling by preventing the GDF15-driven interaction of RET with GFRAL on the cell surface. Treatment with 3P10 reverses excessive lipid oxidation in tumor-bearing mice and prevents cancer cachexia, even under calorie-restricted conditions. Mechanistically, activation of the GFRAL-RET pathway induces expression of genes involved in lipid metabolism in adipose tissues, and both peripheral chemical sympathectomy and loss of adipose triglyceride lipase protect mice from GDF15-induced weight loss. These data uncover a peripheral sympathetic axis by which GDF15 elicits a lipolytic response in adipose tissue independently of anorexia, leading to reduced adipose and muscle mass and function in tumor-bearing mice.

PubMed: 32661391
DOI: 10.1038/s41591-020-0945-x

実験手法

X-RAY DIFFRACTION (2.91 Å)