Literature DB >> 2430580

[Structural-functional characteristics of argiopine--the ion channel blockers from the spider Argiope lobata venom].

E V Grishin, T M Volkova, A S Arsen'ev, O S Reshetova, V V Onoprienko.   

Abstract

Argiopine, a compound capable of blocking the glutamate-activated ion channels in experiments with glutamatergic synapses of blowfly larvae, was isolated from the venom of spider Argiope lobata. Argiopine-receptor complex has KD 6,7 X 10(-7) M. The venom solution was treated with 60% ethanol, centrifuged and supernatant was subjected to reversed-phase HPLC in the acetonitrile concentration gradient. Argiopine structure was established using 1H- and 13C-NMR spectroscopy, mass spectrometry, elemental and amino acid analyses. Argiopine (molecular mass 636) consists of arginine (free alpha-NH2) linke with polyamine--NH (CH2)3NH(CH2)3NH(CH2)5NH--through a peptide bond. The polyamine is connected to the alpha-carboxyl group of asparagine whose alpha-amino group is linked to 2,4-dihydroxyphenylacetic acid.

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Year:  1986        PMID: 2430580

Source DB:  PubMed          Journal:  Bioorg Khim        ISSN: 0132-3423


  11 in total

1.  Neurotoxic acylpolyamines from spider venoms.

Authors:  K D McCormick; J Meinwald
Journal:  J Chem Ecol       Date:  1993-10       Impact factor: 2.626

Review 2.  The role of glia in stress: polyamines and brain disorders.

Authors:  Serguei N Skatchkov; Michel A Woodbury-Fariña; Misty Eaton
Journal:  Psychiatr Clin North Am       Date:  2014-11-25

3.  Structure of membrane-active toxin from crab spider Heriaeus melloteei suggests parallel evolution of sodium channel gating modifiers in Araneomorphae and Mygalomorphae.

Authors:  Antonina A Berkut; Steve Peigneur; Mikhail Yu Myshkin; Alexander S Paramonov; Ekaterina N Lyukmanova; Alexander S Arseniev; Eugene V Grishin; Jan Tytgat; Zakhar O Shenkarev; Alexander A Vassilevski
Journal:  J Biol Chem       Date:  2014-10-28       Impact factor: 5.157

4.  Design, synthesis, and biological evaluation of spider toxin (argiotoxin-636) analogs as NMDA receptor antagonists.

Authors:  S T Moe; D L Smith; Y Chien; J L Raszkiewicz; L D Artman; A L Mueller
Journal:  Pharm Res       Date:  1998-01       Impact factor: 4.200

5.  Binding of ArgTX-636 in the NMDA receptor ion channel.

Authors:  Mette H Poulsen; Jacob Andersen; Rune Christensen; Kasper B Hansen; Stephen F Traynelis; Kristian Strømgaard; Anders Skov Kristensen
Journal:  J Mol Biol       Date:  2014-05-24       Impact factor: 5.469

6.  Mechanisms of Channel Block in Calcium-Permeable AMPA Receptors.

Authors:  Edward C Twomey; Maria V Yelshanskaya; Alexander A Vassilevski; Alexander I Sobolevsky
Journal:  Neuron       Date:  2018-08-16       Impact factor: 17.173

7.  Structure and synthesis of a potent glutamate receptor antagonist in wasp venom.

Authors:  A T Eldefrawi; M E Eldefrawi; K Konno; N A Mansour; K Nakanishi; E Oltz; P N Usherwood
Journal:  Proc Natl Acad Sci U S A       Date:  1988-07       Impact factor: 11.205

8.  Kainate-induced calcium overload of cortical neurons in vitro: Dependence on expression of AMPAR GluA2-subunit and down-regulation by subnanomolar ouabain.

Authors:  Polina A Abushik; Dmitry A Sibarov; Misty J Eaton; Serguei N Skatchkov; Sergei M Antonov
Journal:  Cell Calcium       Date:  2013-05-28       Impact factor: 6.817

9.  Antagonism of responses to excitatory amino acids on rat cortical neurones by the spider toxin, argiotoxin636.

Authors:  T Priestley; G N Woodruff; J A Kemp
Journal:  Br J Pharmacol       Date:  1989-08       Impact factor: 8.739

10.  Polyamines as Snake Toxins and Their Probable Pharmacological Functions in Envenomation.

Authors:  Steven D Aird; Alejandro Villar Briones; Michael C Roy; Alexander S Mikheyev
Journal:  Toxins (Basel)       Date:  2016-09-26       Impact factor: 4.546

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