Abstract
The receptor for alpha-latrotoxin, the major protein component of the black widow spider venom, was investigated by the use of the purified toxin and of polyclonal, monospecific anti-alpha-latrotoxin antibodies. Experiments on rat brain synaptosomes (where the existence of alpha- latrotoxin receptors was known from previous studies) demonstrated that the toxin-receptor complex is made stable by glutaraldehyde fixation. At saturation, each such complex was found to bind on the average five antitoxin antibody molecules. In frog cutaneous pectoris muscles, the existence of a finite number of high-affinity receptors was revealed by binding experiments with 125I-alpha-latrotoxin (Kd = 5 X 10(-10) M; bmax = 1.36 +/- 0.16 [SE] X 10(9) sites/mg tissue, dry weight). Nonpermeabilized muscles were first treated with alpha-latrotoxin, and then washed, fixed, dissociated into individual fibers, and treated with anti-alpha-latrotoxin antibodies and finally with rhodamine- conjugated sheep anti-rabbit antibodies. In these preparations, muscle fibers and unmyelinated preterminal nerve branches were consistently negative, whereas bright specific fluorescent images, indicative of concentrated alpha-latrotoxin binding sites, appeared in the junctional region. These images closely correspond in size, shape, and localization to endplates decorated by the acetylcholinesterase reaction. The presynaptic localization of the specific fluorescence found at frog neuromuscular junctions is supported by two sets of findings: (a) fluorescent endplate images were not seen in muscles that had been denervated; and (b) the distribution of fluorescence in many fibers treated with alpha-latrotoxin at room temperature was the one expected from swollen terminal branches. Swelling of terminals is a known morphological change induced by alpha-latrotoxin in this preparation. When muscles were treated with either proteolytic enzymes (trypsin, collagenase) or detergents (Triton X-100) before exposure to alpha-latrotoxin, the specific fluorescent endplate images failed to appear. Taken together these findings indicate that the alpha- latrotoxin receptor is an externally exposed protein highly concentrated in the nerve terminal plasma membrane. Its density (number per unit area) at the frog neuromuscular junction can be calculated to be approximately 2,400/micron2.
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Selected References
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- Baba A., Cooper J. R. The action of black widow spider venom on cholinergic mechanisms in synaptosomes. J Neurochem. 1980 Jun;34(6):1369–1379. doi: 10.1111/j.1471-4159.1980.tb11217.x. [DOI] [PubMed] [Google Scholar]
- Ceccarelli B., Grohovaz F., Hurlbut W. P. Freeze-fracture studies of frog neuromuscular junctions during intense release of neurotransmitter. I. Effects of black widow spider venom and Ca2+-free solutions on the structure of the active zone. J Cell Biol. 1979 Apr;81(1):163–177. doi: 10.1083/jcb.81.1.163. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ceccarelli B., Hurlbut W. P. Ca2+-dependent recycling of synaptic vesicles at the frog neuromuscular junction. J Cell Biol. 1980 Oct;87(1):297–303. doi: 10.1083/jcb.87.1.297. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ceccarelli B., Hurlbut W. P., Mauro A. Turnover of transmitter and synaptic vesicles at the frog neuromuscular junction. J Cell Biol. 1973 May;57(2):499–524. doi: 10.1083/jcb.57.2.499. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ceccarelli B., Hurlbut W. P. Vesicle hypothesis of the release of quanta of acetylcholine. Physiol Rev. 1980 Apr;60(2):396–441. doi: 10.1152/physrev.1980.60.2.396. [DOI] [PubMed] [Google Scholar]
- Clark A. W., Mauro A., Longenecker H. E., Jr, Hurlbut W. P. Effects of black widow spider venom on the frog neuromuscular junction. Effects on the fine structure of the frog neuromuscular junction. Nature. 1970 Feb 21;225(5234):703–705. doi: 10.1038/225703a0. [DOI] [PubMed] [Google Scholar]
- De Camilli P., Cameron R., Greengard P. Synapsin I (protein I), a nerve terminal-specific phosphoprotein. I. Its general distribution in synapses of the central and peripheral nervous system demonstrated by immunofluorescence in frozen and plastic sections. J Cell Biol. 1983 May;96(5):1337–1354. doi: 10.1083/jcb.96.5.1337. [DOI] [PMC free article] [PubMed] [Google Scholar]
- De Camilli P., Harris S. M., Jr, Huttner W. B., Greengard P. Synapsin I (Protein I), a nerve terminal-specific phosphoprotein. II. Its specific association with synaptic vesicles demonstrated by immunocytochemistry in agarose-embedded synaptosomes. J Cell Biol. 1983 May;96(5):1355–1373. doi: 10.1083/jcb.96.5.1355. [DOI] [PMC free article] [PubMed] [Google Scholar]
- De Camilli P., Ueda T., Bloom F. E., Battenberg E., Greengard P. Widespread distribution of protein I in the central and peripheral nervous systems. Proc Natl Acad Sci U S A. 1979 Nov;76(11):5977–5981. doi: 10.1073/pnas.76.11.5977. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dolly J. O., Black J., Williams R. S., Melling J. Acceptors for botulinum neurotoxin reside on motor nerve terminals and mediate its internalization. Nature. 1984 Feb 2;307(5950):457–460. doi: 10.1038/307457a0. [DOI] [PubMed] [Google Scholar]
- Dreyer F., Peper K. A monolayer preparation of innervated skeletal muscle fibres of the m. cutaneus pectoris of the frog. Pflugers Arch. 1974 Apr 22;348(3):257–262. doi: 10.1007/BF00587416. [DOI] [PubMed] [Google Scholar]
- Frontali N., Ceccarelli B., Gorio A., Mauro A., Siekevitz P., Tzeng M. C., Hurlbut W. P. Purification from black widow spider venom of a protein factor causing the depletion of synaptic vesicles at neuromuscular junctions. J Cell Biol. 1976 Mar;68(3):462–479. doi: 10.1083/jcb.68.3.462. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gorio A., Rubin L. L., Mauro A. Double mode of action of black widow spider venom on frog neuromuscular junction. J Neurocytol. 1978 Apr;7(2):193–202. doi: 10.1007/BF01217918. [DOI] [PubMed] [Google Scholar]
- Grasso A., Pelliccia M., Alemà S. Characterization of alpha-latrotoxin interaction with rat brain synaptosomes and PC12 cells. Toxicon. 1982;20(1):149–156. doi: 10.1016/0041-0101(82)90184-2. [DOI] [PubMed] [Google Scholar]
- Grasso A., Senni M. I. A toxin purified from the venom of black widow spider affects the uptake and release of radioactive gamma-amino butyrate and N-epinephrine from rat brain synaptosomes. Eur J Biochem. 1979 Dec 17;102(2):337–344. doi: 10.1111/j.1432-1033.1979.tb04248.x. [DOI] [PubMed] [Google Scholar]
- Hajós F. An improved method for the preparation of synaptosomal fractions in high purity. Brain Res. 1975 Aug 15;93(3):485–489. doi: 10.1016/0006-8993(75)90186-9. [DOI] [PubMed] [Google Scholar]
- Hooper J. E., Carlson S. S., Kelly R. B. Antibodies to synaptic vesicles purified from Narcine electric organ bind a subclass of mammalian nerve terminals. J Cell Biol. 1980 Oct;87(1):104–113. doi: 10.1083/jcb.87.1.104. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Howard B. D., Gundersen C. B., Jr Effects and mechanisms of polypeptide neurotoxins that act presynaptically. Annu Rev Pharmacol Toxicol. 1980;20:307–336. doi: 10.1146/annurev.pa.20.040180.001515. [DOI] [PubMed] [Google Scholar]
- Hurlbut W. P., Ceccarelli B. Transmitter release and recycling of synaptic vesicle membrane at the neuromuscular junction. Adv Cytopharmacol. 1974;2:141–154. [PubMed] [Google Scholar]
- Hurlbut W. P., Ceccarelli B. Use of black widow spider venom to study the release of neurotransmitters. Adv Cytopharmacol. 1979;3:87–115. [PubMed] [Google Scholar]
- Huttner W. B., Schiebler W., Greengard P., De Camilli P. Synapsin I (protein I), a nerve terminal-specific phosphoprotein. III. Its association with synaptic vesicles studied in a highly purified synaptic vesicle preparation. J Cell Biol. 1983 May;96(5):1374–1388. doi: 10.1083/jcb.96.5.1374. [DOI] [PMC free article] [PubMed] [Google Scholar]
- KARNOVSKY M. J., ROOTS L. A "DIRECT-COLORING" THIOCHOLINE METHOD FOR CHOLINESTERASES. J Histochem Cytochem. 1964 Mar;12:219–221. doi: 10.1177/12.3.219. [DOI] [PubMed] [Google Scholar]
- LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
- Letinsky M. S., Fischbeck K. H., McMahan U. J. Precision of reinnervation of original postsynaptic sites in frog muscle after a nerve crush. J Neurocytol. 1976 Dec;5(6):691–718. doi: 10.1007/BF01181582. [DOI] [PubMed] [Google Scholar]
- Longenecker H. E., Jr, Hurlbut W. P., Mauro A., Clark A. W. Effects of black widow spider venom on the frog neuromuscular junction. Effects on end-plate potential, miniature end-plate potential and nerve terminal spike. Nature. 1970 Feb 21;225(5234):701–703. doi: 10.1038/225701a0. [DOI] [PubMed] [Google Scholar]
- Matthew W. D., Tsavaler L., Reichardt L. F. Identification of a synaptic vesicle-specific membrane protein with a wide distribution in neuronal and neurosecretory tissue. J Cell Biol. 1981 Oct;91(1):257–269. doi: 10.1083/jcb.91.1.257. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Meldolesi J., Madeddu L., Torda M., Gatti G., Niutta E. The effect of alpha-latrotoxin on the neurosecretory PC12 cell line: studies on toxin binding and stimulation of transmitter release. Neuroscience. 1983 Nov;10(3):997–1009. doi: 10.1016/0306-4522(83)90238-5. [DOI] [PubMed] [Google Scholar]
- Meldolesi J. Studies on alpha-latrotoxin receptors in rat brain synaptosomes: correlation between toxin binding and stimulation of transmitter release. J Neurochem. 1982 Jun;38(6):1559–1569. doi: 10.1111/j.1471-4159.1982.tb06633.x. [DOI] [PubMed] [Google Scholar]
- Morel N., Manaranche R., Israël M., Gulik-Krzywicki T. Isolation of a presynaptic plasma membrane fraction from Torpedo cholinergic synaptosomes: evidence for a specific protein. J Cell Biol. 1982 May;93(2):349–356. doi: 10.1083/jcb.93.2.349. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Morel N., Thieffry M., Manaranche R. Binding of a Glycera convoluta neurotoxin to cholinergic nerve terminal plasma membranes. J Cell Biol. 1983 Dec;97(6):1737–1744. doi: 10.1083/jcb.97.6.1737. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Peper K., Dreyer F., Sandri C., Akert K., Moor H. Structure and ultrastructure of the frog motor endplate. A freeze-etching study. Cell Tissue Res. 1974 Jun 24;149(4):437–455. doi: 10.1007/BF00223024. [DOI] [PubMed] [Google Scholar]
- Reichardt L. F., Kelly R. B. A molecular description of nerve terminal function. Annu Rev Biochem. 1983;52:871–926. doi: 10.1146/annurev.bi.52.070183.004255. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schultz G. S., Sarras M. P., Jr, Gunther G. R., Hull B. E., Alicea H. A., Gorelick F. S., Jamieson J. D. Guinea pig pancreatic acini prepared with purified collagenase. Exp Cell Res. 1980 Nov;130(1):49–62. doi: 10.1016/0014-4827(80)90041-5. [DOI] [PubMed] [Google Scholar]
- Tzeng M. C., Cohen R. S., Siekevitz P. Release of neurotransmitters and depletion of synaptic vesicles in cerebral cortex slices by alpha-latrotoxin from black widow spider venom. Proc Natl Acad Sci U S A. 1978 Aug;75(8):4016–4020. doi: 10.1073/pnas.75.8.4016. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tzeng M. C., Siekevitz P. The binding interaction between alpha-latrotoxin from black widow spider venom and a dog cerebral cortex synaptosomal membrane preparation. J Neurochem. 1979 Jul;33(1):263–274. doi: 10.1111/j.1471-4159.1979.tb11728.x. [DOI] [PubMed] [Google Scholar]
- Walker J. H., Jones R. T., Obrocki J., Richardson G. P., Stadler H. Presynaptic plasma membranes and synaptic vesicles of cholinergic nerve endings demonstrated by means of specific antisera. Cell Tissue Res. 1982;223(1):101–116. doi: 10.1007/BF00221502. [DOI] [PubMed] [Google Scholar]
- Walker J. H., Obrocki J., Zimmermann C. W. Identification of a proteoglycan antigen characteristic of cholinergic synaptic vesicles. J Neurochem. 1983 Jul;41(1):209–216. doi: 10.1111/j.1471-4159.1983.tb11829.x. [DOI] [PubMed] [Google Scholar]
- Watanabe O., Meldolesi J. The effects of alpha-latrotoxin of black widow spider venom on synaptosome ultrastructure. A morphometric analysis correlating its effects on transmitter release. J Neurocytol. 1983 Jun;12(3):517–531. doi: 10.1007/BF01159388. [DOI] [PubMed] [Google Scholar]