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2.8 Å Resolution Crystal Structure of Human TRAIL, a Cytokine with Selective Antitumor Activity

Authors :
Yo Han Choi
Sun Shin Cha
Min Sung Kim
Hang-Cheol Shin
Nam Kyu Shin
Byung-Ha Oh
Byung-Je Sung
Young Chul Sung
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.

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