Back to Search
Start Over
2.8 Å Resolution Crystal Structure of Human TRAIL, a Cytokine with Selective Antitumor Activity
- Source :
- Immunity. (2):253-261
- Publisher :
- Cell Press.
-
Abstract
- TRAIL is a newly identified cytokine belonging to the large tumor necrosis factor (TNF) family. TRAIL is a novel molecule inducing apoptosis in a wide variety of tumor cells but not in normal cells. To help in elucidating its biological roles and designing mutants with improved therapeutic potential, we have determined the crystal structure of human TRAIL. The structure reveals that a unique frame insertion of 12–16 amino acids adopts a salient loop structure penetrating into the receptor-binding site. The loop drastically alters the common receptor-binding surface of the TNF family most likely for the specific recognition of cognate partners. A structure-based mutagenesis study demonstrates a critical role of the insertion loop in the cytotoxic activity of TRAIL.
- Subjects :
- medicine.medical_treatment
Molecular Sequence Data
Immunology
Mutant
Mutagenesis (molecular biology technique)
Biology
Receptors, Tumor Necrosis Factor
TNF-Related Apoptosis-Inducing Ligand
Structure-Activity Relationship
Osteoprotegerin
Antigens, CD
medicine
Humans
Immunology and Allergy
Cytotoxic T cell
Amino Acid Sequence
Lymphotoxin-alpha
chemistry.chemical_classification
Binding Sites
Crystallography
Membrane Glycoproteins
Tumor Necrosis Factor-alpha
Cell biology
Amino acid
Receptors, TNF-Related Apoptosis-Inducing Ligand
Infectious Diseases
Cytokine
chemistry
Receptors, Tumor Necrosis Factor, Type I
Apoptosis
Mutation
Tumor necrosis factor alpha
Apoptosis Regulatory Proteins
Subjects
Details
- Language :
- English
- ISSN :
- 10747613
- Issue :
- 2
- Database :
- OpenAIRE
- Journal :
- Immunity
- Accession number :
- edsair.doi.dedup.....ebf41b4ca442de8f5fa8080076f41c07
- Full Text :
- https://doi.org/10.1016/S1074-7613(00)80100-4