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Receptor Specificity Engineering of TNF Superfamily Ligands
被引:10
作者:
Suo, Fengzhi
[1
]
Zhou, Xinyu
[1
]
Setroikromo, Rita
[1
]
Quax, Wim J.
[1
]
机构:
[1] Univ Groningen, Dept Chem & Pharmaceut Biol, Groningen Res Inst Pharm, Antonius Deusinglaan 1, NL-9713 AV Groningen, Netherlands
关键词:
TNF family;
protein engineering;
receptor specificity;
ligand;
TNF-alpha;
TRAIL;
RANKL;
APOPTOSIS-INDUCING LIGAND;
LYMPHOTOXIN-BETA RECEPTOR;
NECROSIS-FACTOR RECEPTORS;
NF-KAPPA-B;
CRYSTAL-STRUCTURE;
MEDIATED APOPTOSIS;
SIGNALING PATHWAYS;
SELECTIVE MUTANTS;
TRAIL VARIANTS;
DECOY RECEPTOR;
D O I:
10.3390/pharmaceutics14010181
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
The tumor necrosis factor (TNF) ligand family has nine ligands that show promiscuity in binding multiple receptors. As different receptors transduce into diverse pathways, the study on the functional role of natural ligands is very complex. In this review, we discuss the TNF ligands engineering for receptor specificity and summarize the performance of the ligand variants in vivo and in vitro. Those variants have an increased binding affinity to specific receptors to enhance the cell signal conduction and have reduced side effects due to a lowered binding to untargeted receptors. Refining receptor specificity is a promising research strategy for improving the application of multi-receptor ligands. Further, the settled variants also provide experimental guidance for engineering receptor specificity on other proteins with multiple receptors.
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页数:20
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