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Expression, purification and crystallization of recombinant human TRAIL.

作者信息

Cha S S, Shin H C, Choi K Y, Oh B H

机构信息

Department of Life Science and School of Environmental Engineering, Pohang University of Science and Technology, Pohang, Kyungbuk 790-784, South Korea.

出版信息

Acta Crystallogr D Biol Crystallogr. 1999 May;55(Pt 5):1101-4. doi: 10.1107/s090744499900164x.

Abstract

TRAIL (also known as Apo-2L) belongs to the tumour necrosis factor (TNF) cytokine family and induces rapid apoptosis in a wide variety of tumour cell lines upon binding to the death-signalling receptors on the cell membrane. Normal cells are resistant to TRAIL, owing to the expression of decoy receptors which lack functional death domains and antagonize TRAIL-induced apoptosis. Soluble and functional human TRAIL, expressed in Escherichia coli and refolded into a functional form, has been crystallized. The crystals belong to space group P63 with unit-cell dimensions a = b = 65.61, c = 131. 70 A. The asymmetric unit contains two molecules of TRAIL, with a crystal volume per protein mass (Vm) of 2.41 A3 Da-1 and a solvent content of about 42% by volume. A native and a platinum-derivative data set to 2.8 and 3.5 A resolution, respectively, were obtained from frozen crystals. Structure determination by a combined molecular replacement and isomorphous replacement method is in progress.

摘要

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