Cell-free synthesis and combinatorial selective 15 N-labeling of the cytotoxic protein amoebapore A from Entamoeba histolytica

RIS ID

29051

Publication Details

Xun, Y., Tremouilhac, P., Carraher, C., Gelhaus, C., Ozawa, K., Otting, G., Dixon, N. E., Leippe, M., Grotzinger, J., Dingley, A. J. & Kralicek, A. V. (2009). Cell-free synthesis and combinatorial selective 15 N-labeling of the cytotoxic protein amoebapore A from Entamoeba histolytica. Protein Expression and Purification, 68 (1), 22-27.

Abstract

Amoebapore A is a pore-forming protein produced by the pathogenic parasite Entamoeba histolytica, which causes human amoebic dysentery. The pore-forming activity of amoebapore A is regulated by pH-dependent dimerization, a prerequisite for membrane insertion and pore formation. Understanding of these important processes has been hampered by the cytotoxicity of amoebapore A, which prevents the production of this protein in cell-based expression systems. In this study, a protocol for the cell-free production of active recombinant amoebapore A is presented. Protein yields of ∼500 μg/ml of cell-free reaction were achieved. Recombinant amoebapore A was purified using a three-step procedure. To facilitate the structural characterization of the dimeric and pore forms, we adapted the cell-free system to isotope label amoebapore A for NMR studies. The preliminary assignment of a 2D 1H–15N HSQC spectrum of a uniformly 13C/15N-labeled sample was achieved using a combinatorial selective 15N-labeling approach coupled with available 1HN chemical shift data, resulting in the unambiguous assignment of resonances from 55 of the 77 residues. To confirm these results and obtain the full sequence-specific assignments of the 2D 1H–15N HSQC spectrum, a 3D HNCA spectrum was recorded. These assignment data will be used to aid the characterization of amoebapore A dimer formation and membrane insertion.

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Link to publisher version (DOI)

http://dx.doi.org/10.1016/j.pep.2009.06.017