Abstract
The positive charge concentrated at the C-terminal region of ammodytoxin (Atx) A, which is involved in presynaptic toxicity, has been reversed. A six-site mutant of AtxA (K108N/K111N/K127T/K128E/E129T/K132E , where K108N=Lys(108)-->Asn etc. ) was prepared, in which five out of seven C-terminal basic amino acid residues were substituted with neutral or acidic ones. The mutant was approximately 30-fold less lethal, but still neurotoxic. Consistent with this, its binding affinity for the neuronal receptors decreased by only a factor of five. Additionally, a single-site mutant of AtxA was prepared, with substitution at only one position (K127T) out of six mutated in the six-site mutant. Its toxicity indicated that most, if not all, of the six mutated residues partially contribute to the decreased lethality of the multiple-site mutant.
Full Text
The Full Text of this article is available as a PDF (125.2 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Chang C. C., Su M. J. Mutual potentiation, at nerve terminals, between toxins from snake venoms which contain phospholipase A activity: beta-bungarotoxin, crotoxin, taipoxin. Toxicon. 1980;18(5-6):641–648. doi: 10.1016/0041-0101(80)90092-6. [DOI] [PubMed] [Google Scholar]
- Curin-Serbec V., Délot E., Faure G., Saliou B., Gubensek F., Bon C., Choumet V. Antipeptide antibodies directed to the C-terminal part of ammodytoxin A react with the PLA2 subunit of crotoxin and neutralize its pharmacological activity. Toxicon. 1994 Nov;32(11):1337–1348. doi: 10.1016/0041-0101(94)90406-5. [DOI] [PubMed] [Google Scholar]
- Curin-Serbec V., Novak D., Babnik J., Turk D., Gubensek F. Immunological studies of the toxic site in ammodytoxin A. FEBS Lett. 1991 Mar 11;280(1):175–178. doi: 10.1016/0014-5793(91)80231-q. [DOI] [PubMed] [Google Scholar]
- Dennis E. A. Diversity of group types, regulation, and function of phospholipase A2. J Biol Chem. 1994 May 6;269(18):13057–13060. [PubMed] [Google Scholar]
- Dennis E. A. Kinetic dependence of phospholipase A 2 activity on the detergent Triton X-100. J Lipid Res. 1973 Mar;14(2):152–159. [PubMed] [Google Scholar]
- Gelb M. H., Jain M. K., Hanel A. M., Berg O. G. Interfacial enzymology of glycerolipid hydrolases: lessons from secreted phospholipases A2. Annu Rev Biochem. 1995;64:653–688. doi: 10.1146/annurev.bi.64.070195.003253. [DOI] [PubMed] [Google Scholar]
- Hains P. G., Ramsland P. A., Broady K. W. Modeling of acanthoxin A1, a PLA2 enzyme from the venom of the common death adder (Acanthophis antarcticus). Proteins. 1999 Apr 1;35(1):80–88. doi: 10.1002/(sici)1097-0134(19990401)35:1<80::aid-prot8>3.0.co;2-3. [DOI] [PubMed] [Google Scholar]
- Kini R. M., Iwanaga S. Structure-function relationships of phospholipases. I: Prediction of presynaptic neurotoxicity. Toxicon. 1986;24(6):527–541. doi: 10.1016/0041-0101(86)90173-x. [DOI] [PubMed] [Google Scholar]
- Kondo K., Zhang J., Xu K., Kagamiyama H. Amino acid sequence of a presynaptic neurotoxin, agkistrodotoxin, from the venom of Agkistrodon halys Pallas. J Biochem. 1989 Feb;105(2):196–203. doi: 10.1093/oxfordjournals.jbchem.a122639. [DOI] [PubMed] [Google Scholar]
- Krizaj I., Dolly J. O., Gubensek F. Identification of the neuronal acceptor in bovine cortex for ammodytoxin C, a presynaptically neurotoxic phospholipase A2. Biochemistry. 1994 Nov 22;33(46):13938–13945. doi: 10.1021/bi00250a049. [DOI] [PubMed] [Google Scholar]
- Krizaj I., Liang N. S., Pungercar J., Strukelj B., Ritonja A., Gubensek F. Amino acid and cDNA sequences of a neutral phospholipase A2 from the long-nosed viper (Vipera ammodytes ammodytes) venom. Eur J Biochem. 1992 Mar 15;204(3):1057–1062. doi: 10.1111/j.1432-1033.1992.tb16728.x. [DOI] [PubMed] [Google Scholar]
- Krizaj I., Turk D., Ritonja A., Gubensek F. Primary structure of ammodytoxin C further reveals the toxic site of ammodytoxin. Biochim Biophys Acta. 1989 Nov 30;999(2):198–202. doi: 10.1016/0167-4838(89)90218-5. [DOI] [PubMed] [Google Scholar]
- Perkins S. J. Protein volumes and hydration effects. The calculations of partial specific volumes, neutron scattering matchpoints and 280-nm absorption coefficients for proteins and glycoproteins from amino acid sequences. Eur J Biochem. 1986 May 15;157(1):169–180. doi: 10.1111/j.1432-1033.1986.tb09653.x. [DOI] [PubMed] [Google Scholar]
- Pungercar J., Krizaj I., Liang N. S., Gubensek F. An aromatic, but not a basic, residue is involved in the toxicity of group-II phospholipase A2 neurotoxins. Biochem J. 1999 Jul 1;341(Pt 1):139–145. [PMC free article] [PubMed] [Google Scholar]
- Renetseder R., Brunie S., Dijkstra B. W., Drenth J., Sigler P. B. A comparison of the crystal structures of phospholipase A2 from bovine pancreas and Crotalus atrox venom. J Biol Chem. 1985 Sep 25;260(21):11627–11634. [PubMed] [Google Scholar]
- Ritonja A., Gubensek F. Ammodytoxin A, a highly lethal phospholipase A2 from Vipera ammodytes ammodytes venom. Biochim Biophys Acta. 1985 Apr 29;828(3):306–312. doi: 10.1016/0167-4838(85)90312-7. [DOI] [PubMed] [Google Scholar]
- Sanger F., Nicklen S., Coulson A. R. DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463–5467. doi: 10.1073/pnas.74.12.5463. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Scott D. L., Mandel A. M., Sigler P. B., Honig B. The electrostatic basis for the interfacial binding of secretory phospholipases A2. Biophys J. 1994 Aug;67(2):493–504. doi: 10.1016/S0006-3495(94)80546-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tang L., Zhou Y. C., Lin Z. J. Crystal structure of agkistrodotoxin, a phospholipase A2-type presynaptic neurotoxin from agkistrodon halys pallas. J Mol Biol. 1998 Sep 11;282(1):1–11. doi: 10.1006/jmbi.1998.1987. [DOI] [PubMed] [Google Scholar]
- Thouin L. G., Jr, Ritonja A., Gubensek F., Russell F. E. Neuromuscular and lethal effects of phospholipase A from Vipera ammodytes venom. Toxicon. 1982;20(6):1051–1058. doi: 10.1016/0041-0101(82)90107-6. [DOI] [PubMed] [Google Scholar]
- Tsai I. H., Liu H. C., Chang T. Toxicity domain in presynaptically toxic phospholipase A2 of snake venom. Biochim Biophys Acta. 1987 Nov 5;916(1):94–99. doi: 10.1016/0167-4838(87)90215-9. [DOI] [PubMed] [Google Scholar]
