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Construction and characterization of two versions of bifunctional EGFP–sTRAIL fusion proteins.

Authors :
Jiayin Shen
Yifan Wu
Lijun Shi
Junhong Liu
Shunyi Liu
Zhengbing Guan
Zhimin Yin
Source :
Applied Microbiology & Biotechnology; Aug2007, Vol. 76 Issue 1, p141-149, 9p, 1 Color Photograph, 1 Black and White Photograph, 1 Chart, 5 Graphs
Publication Year :
2007

Abstract

The extracellular portion (amino acids 95–281 or 114–281) of the human tumor necrosis factor-related apoptosis-inducing ligand (sTRAIL) was genetically linked to the C terminus of the fluoresce-enhanced green fluorescent protein variant (EGFP) to generate two versions of EGFP–sTRAIL fusion proteins, designated EGFP–sTR95 and EGFP–sTR114, respectively. The two versions of EGFP–sTRAIL fusion proteins both induce extensive apoptosis in lymphoid as well as nonlymphoid tumor cell lines. In addition, the two versions of fusion proteins retain similar fluorescence spectra to those of EGFP and have shown the specific binding to TRAIL receptor-positive cells; thus, the stained cells could be analyzed with flow cytometry. Hence, the two versions of fusion proteins represent a readily obtainable source of biologically active sTRAIL that may prove useful in exploit fully the characteristics of both the soluble TRAIL and its receptor system. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01757598
Volume :
76
Issue :
1
Database :
Complementary Index
Journal :
Applied Microbiology & Biotechnology
Publication Type :
Academic Journal
Accession number :
25971523
Full Text :
https://doi.org/10.1007/s00253-007-1001-1