Tetrapandins, a New Class of Scorpion Toxins That Specifically Inhibit Store-operated Calcium Entry in Human Embryonic Kidney-293 Cells*

Venoms from 14 snakes and four scorpions were screened for inhibitory activities toward store-operated Ca2+ entry (SOCE) in human embryonic kidney-293 cells. An inhibitory activity was found in venom from the African scorpion Pandinus imperator. The active agent of this venom was purified by gel filtration and reverse-phase high pressure liquid chromatography methods. Sequence information on the purified fraction, by automatic Edman degradation and mass spectrometry analysis, identified the activity as being contained in two tetrapeptides, which we have named tetrapandins. We demonstrate that synthesized tetrapandins have inhibitory activity for SOCE in human embryonic kidney-293 cells while having no effect on either thapsigargin- or carbachol-stimulated release of Ca2+ stores. These toxins should be extremely useful in future studies to determine downstream events regulated by SOCE as well as to determine whether multiple pathways exist for thapsigargin-stimulated Ca2+ entry.

[1]  G. Fiskum,et al.  Cyclosporin A-insensitive Permeability Transition in Brain Mitochondria , 2003, Journal of Biological Chemistry.

[2]  M. Berridge,et al.  2-Aminoethoxydiphenyl borate (2-APB) antagonises inositol 1,4,5-trisphosphate-induced calcium release, inhibits calcium pumps and has a use-dependent and slowly reversible action on store-operated calcium entry channels. , 2003, Cell calcium.

[3]  J. Putney,et al.  2-aminoethoxydiphenyl borane activates a novel calcium-permeable cation channel. , 2003, Molecular pharmacology.

[4]  D. Ypey,et al.  Besides affecting intracellular calcium signaling, 2‐APB reversibly blocks gap junctional coupling in confluent monolayers, thereby allowing the measurement of single‐cell membrane currents in undissociated cells , 2003, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[5]  R. Payne,et al.  2-Aminoethoxydiphenyl borate inhibits phototransduction and blocks voltage-gated potassium channels in Limulus ventral photoreceptors. , 2002, Cell calcium.

[6]  M. Berridge,et al.  Calcium Signalling: More Messengers, More Channels, More Complexity , 2002, Current Biology.

[7]  Lauren Mackenzie,et al.  2‐Aminoethoxydiphenyl borate (2‐APB) is a reliable blocker of store‐operated Ca2+ entry but an inconsistent inhibitor of InsP3‐induced Ca2+ release , 2002, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[8]  O. Smart,et al.  Inhibition of SERCA Ca2+ pumps by 2-aminoethoxydiphenyl borate (2-APB). 2-APB reduces both Ca2+ binding and phosphoryl transfer from ATP, by interfering with the pathway leading to the Ca2+-binding sites. , 2002, European journal of biochemistry.

[9]  G. Babnigg,et al.  The Role of Endogenous Human Trp4 in Regulating Carbachol-induced Calcium Oscillations in HEK-293 Cells* , 2002, The Journal of Biological Chemistry.

[10]  Christian R. Halaszovich,et al.  The TRP family of cation channels: probing and advancing the concepts on receptor-activated calcium entry , 2002, Progress in Neurobiology.

[11]  M. Vieytes,et al.  Maitotoxin-induced calcium entry in human lymphocytes: modulation by yessotoxin, Ca(2+) channel blockers and kinases. , 2001, Cellular signalling.

[12]  S. Pennington,et al.  Regulation of growth factor induced gene expression by calcium signalling: Integrated mRNA and protein expression analysis , 2001, Proteomics.

[13]  J. Putney,et al.  Mechanisms of capacitative calcium entry. , 2001, Journal of cell science.

[14]  J. Putney,et al.  Signaling Pathways Underlying Muscarinic Receptor-induced [Ca2+] i Oscillations in HEK293 Cells* , 2001, The Journal of Biological Chemistry.

[15]  M. Corona,et al.  Peptides and genes coding for scorpion toxins that affect ion-channels. , 2000, Biochimie.

[16]  L. Possani,et al.  Scorpine, an anti‐malaria and anti‐bacterial agent purified from scorpion venom , 2000, FEBS letters.

[17]  K. Mikoshiba,et al.  Requirement of the inositol trisphosphate receptor for activation of store-operated Ca2+ channels. , 2000, Science.

[18]  G. Babnigg,et al.  Functional significance of human trp1 and trp3 in store-operated Ca(2+) entry in HEK-293 cells. , 2000, American journal of physiology. Cell physiology.

[19]  M. Delepierre,et al.  Scorpion toxins specific for Na+-channels. , 1999, European journal of biochemistry.

[20]  L. Possani,et al.  Structure and function of scorpion toxins affecting K+-channels , 1999 .

[21]  L. Possani,et al.  Peptide toxins as probes of ryanodine receptor structure and function. , 1998, Trends in cardiovascular medicine.

[22]  R. Penner,et al.  Store depletion and calcium influx. , 1997, Physiological reviews.

[23]  B. Martin,et al.  The Mechanism of Inhibition of Ryanodine Receptor Channels by Imperatoxin I, a Heterodimeric Protein from the Scorpion Pandinus imperator* , 1997, The Journal of Biological Chemistry.

[24]  T. Haller,et al.  Two different store-operated Ca2+ entry pathways in MDCK cells. , 1996, Cell calcium.

[25]  E. Kohn,et al.  The role of calcium in the regulation of invasion and angiogenesis. , 1996, In vivo.

[26]  S. Hong,et al.  Facilitation of nicotinic receptor desensitization at mouse motor endplate by a receptor-operated Ca2+ channel blocker, SK&F 96365. , 1994, European journal of pharmacology.

[27]  W. Lin,et al.  Inhibition of the Sodium Channel by SK&F 96365, an Inhibitor of the Receptor-Operated Calcium Channel, in Mouse Diaphragm. , 1994, Journal of biomedical science.

[28]  T. Pozzan,et al.  Receptor-activated Ca2+ influx: how many mechanisms for how many channels? , 1994, Trends in pharmacological sciences.

[29]  B. Nilius,et al.  Multiple effects of SK&F 96365 on ionic currents and intracellular calcium in human endothelial cells. , 1994, Cell calcium.

[30]  F. Gusovsky,et al.  Maitotoxin effects are blocked by SK&F 96365, an inhibitor of receptor-mediated calcium entry. , 1992, Molecular pharmacology.

[31]  V. Bindokas,et al.  Calcium Channel‐Targeted Polypeptide Toxins a , 1991, Annals of the New York Academy of Sciences.

[32]  D. Hupe,et al.  The inhibition of receptor-mediated and voltage-dependent calcium entry by the antiproliferative L-651,582. , 1991, The Journal of biological chemistry.

[33]  J. Putney,et al.  Uptake and intracellular sequestration of divalent cations in resting and methacholine-stimulated mouse lacrimal acinar cells. Dissociation by Sr2+ and Ba2+ of agonist-stimulated divalent cation entry from the refilling of the agonist-sensitive intracellular pool. , 1990, The Journal of biological chemistry.

[34]  R. Keith,et al.  Inhibition of N‐methyl‐D‐aspartate‐ and kainic acid‐induced neurotransmitter release by ω‐conotoxin GVIA , 1989, British journal of pharmacology.

[35]  W. Schilling,et al.  Characterization of the bradykinin-stimulated calcium influx pathway of cultured vascular endothelial cells. Saturability, selectivity, and kinetics. , 1989, The Journal of biological chemistry.

[36]  J. Putney,et al.  A model for receptor-regulated calcium entry. , 1986, Cell calcium.

[37]  A. Maelicke,et al.  Selective blockage of voltage-dependent K+ channels by a novel scorpion toxin , 1982, Nature.

[38]  Kao Cy TETRODOTOXIN, SAXITOXIN AND THEIR SIGNIFICANCE IN THE STUDY OF EXCITATION PHENOMENA , 1966 .

[39]  L. A. Carpino Synthesis and Oxidation of 2-Amino-2,3-dihydro-1H-benz[de]isoquinoline and 1,2,3,4-Tetrahydronaphtho[1,8-de][1,2]diazepine and Related Cyclic 1,2-Dibenzylhydrazines , 1963 .