Soluble expression, purification and the role of C-terminal glycine residues in scorpion toxin BmK AGP-SYPU2
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The existence of glycine residues in long-chain scorpion toxins has been well documented. However, their role as analgesics has not been evaluated. To address this issue, we investigated the functional role of glycines in the C-terminal end of Chinese-scorpion toxin from Buthus martensii Karsch (BmK AGP-SYPU2) using site-directed mutagenesis and analgesic activity assays. Recombinant BmK AGP-SYPU2 and its mutants were efficiently expressed in E. coli and purified to homogeneity using immobilized metal ion affinity chromatography (IMAC) and cation exchange chromatography. The mouse-twisting test was used to detect the analgesic activity of BmK AGP-SYPU2 and its mutants. As a result, we identified glycines at the C-terminal end that, when altered, significantly affected analgesic activity. Also, Mut6566 was significantly decreased compared to BmK AGP-SYPU2. These data indicate that the glycines at the C-terminal end are important for the analgesic activity of BmK AGP-SYPU2.
Abstract
The existence of glycine residues in long-chain scorpion toxins has been well documented. However, their role as analgesics has not been evaluated. To address this issue, we investigated the functional role of glycines in the C-terminal end of Chinese-scorpion toxin from Buthus martensii Karsch (BmK AGP-SYPU2) using site-directed mutagenesis and analgesic activity assays. Recombinant BmK AGP-SYPU2 and its mutants were efficiently expressed in E. coli and purified to homogeneity using immobilized metal ion affinity chromatography (IMAC) and cation exchange chromatography. The mouse-twisting test was used to detect the analgesic activity of BmK AGP-SYPU2 and its mutants. As a result, we identified glycines at the C-terminal end that, when altered, significantly affected analgesic activity. Also, Mut6566 was significantly decreased compared to BmK AGP-SYPU2. These data indicate that the glycines at the C-terminal end are important for the analgesic activity of BmK AGP-SYPU2.
참고문헌 (25)
- Possani, L. D., "Peptides and genes coding for scorpion toxins that affect ion-channels", Biochimie, 82, pp.861~868 (2000)
- Goudet, C., "An overview of toxins scorpion and genes from the venom of the Asian Buthus martensi Karsch", Toxicon, 40, pp.1239~1258 (2002)
- Lipkind, G. M., "A model of scorpion toxin binding to voltage-gated K+ channels", J. Membr. Biol., 158, pp.187~196 (1997)
- Naranjo, D., "A strongly interacting pair of residues on the contact surface of charybdotoxin and a Shaker K+ channel", Neuron, 16, pp.123~130 (1996)
- Menez, A., "Functional architectures of animal toxins: a clue to drug design?", Toxicon, 36, pp.1557~1572 (1998)
- He, X. L., "Crystal structures of two α-like scorpion toxins: nonproline cis peptide bonds and implications for new binding site selectivity on the sodium channel", J. Mol. Biol., 292, pp.125~135 (1999)
- Kharrat, R., "Structure", activity relationships of scorpion alpha-toxins. Multiple residues contribute to the interaction with receptors, 1989, pp.181, 381~390
- Karbat, I., "Molecular basis of the high insecticidal potency of scorpion alpha-toxins", J. Biol. Chem., 279, pp.31679~31686 (2004)
- Zilberberg, N., "Functional expression and genetic alteration of an alpha scorpion neurotoxin", Biochemistry, 35, pp.10215~10222 (1996)
- Zilberberg, N., "Identification of structural elements of a scorpion alpha-neurotoxin important for receptor site recognition", J. Biol. Chem., 272, pp.14810~14816 (1997)
- Sun, Y. M., "Roles of disulfide bridges in scorpion toxin BmK M1 analyzed by mutagenesis", J. Pept. Res., 60, pp.247~256 (2002)
- Sun, Y. M., "Importance of the conserved aromatic residues in the scorpion alpha-like toxin BmK M1: the hydrophobic surface region revisited", J. Biol. Chem., 278, pp.24125~24131 (2003)
- Wang, C. G., "Exploration of the functional site of a scorpion alpha-like toxin by site-directed mutagenesis", Biochemistry, 42, pp.4699~4708 (2003)
- Cui, Y., "Structure and function relationship of toxin from Chinese scorpion Buthus martensii Karsch (BmK AGAP): gaining insight into related sites of analgesic activity", Peptides, 31, pp.995~1000 (2010)
- Ma, R., "Location of the analgesic domain in scorpion toxin BmK AGAP by mutagenesis of disulfide bridges", Biochem. Biophys. Res. Commun., 394, pp.330~334 (2010)
- Zhu, J., "Solution structure of BmK αTx11, a tox in from the venom of the Chinese scorpion Buthus martensii Karsch", Biochem. Biophys. Res. Commun., 391, pp.627~633 (2010)
- Guex, N., "SWISS-MODEL and the Swiss-PdbViewer: An environment for comparative protein modeling", Electrophoresis, 18, pp.2714~2723 (1997)
- Laskowski, R. A., "PROCHECK: a program to check the stereochemical quality of protein structures", J. Appl. Crystallogr., 26, pp.283~291 (1993)
- Fiordalisi, J. J., "Synthesis and expression in Escherichia coli of a gene for kappa-bungarotoxin", Biochemistry, 30, pp.10337~10343 (1991)
- Bessette, P. H., "Efficient folding of proteins with multiple disulfide bonds in the Escherichia coli cytoplasm", Proc. Natl. Acad. Sci. U.S.A., 통권 : 96, pp.13703~13708 (1999)
- Liu, Z., "Cloning, Co-Expression with an Amidating Enzyme, and Activity of the Scorpion Toxin BmK ITa1 cDNA in Insect Cells", Mol. Biotechnol., 24, pp.21~26 (2003)
- Gurevitz, M., "Diversification of neurotoxins by C-tail ‘wiggling’: a scorpion recipe for survival", FASEB J., 15, pp.1201~1205 (2001)
- Blanc, E., "Solution structure of maurotoxin, a scorpion toxin from Scorpio maurus, with high affinity for voltage-gated potassium channels", Proteins, 29, pp.321~333 (1997)
- Bradford, M. M., "A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding", Anal. Biochem., 72, pp.248~254 (1976)
- Fennessy, M. R., "Methods in Narcotics Research", pp.76~79 (1975), Marcel Dekker
