A proteomic analysis of the early secondary molecular effects caused by Cn2 scorpion toxin on neuroblastoma cells

被引:7
|
作者
Escalona, Martha Pedraza [1 ]
Batista, Cesar V. F. [2 ]
Cassulini, Rita Restano [1 ]
Rios, Marisol Sandoval [1 ]
Coronas, Fredy I. [1 ]
Possani, Lourival D. [1 ]
机构
[1] Univ Nacl Autonoma Mexico, Inst Biotecnol, Dept Med Mol & Bioproc, Cuernavaca 62210, Morelos, Mexico
[2] Univ Nacl Autonoma Mexico, Inst Biotecnol, Lab Univ Proteom, Cuernavaca 62210, Morelos, Mexico
关键词
Bidimensional gel; Cellular events; Mass spectrometry; Proteomic analysis; Scorpion toxin; DORSAL-ROOT GANGLIA; CHANNEL; VENOM; PROTEIN; ACTIVATION; APOPTOSIS; GROWTH; EXPRESSION; INDUCTION; NA(V)1.6;
D O I
10.1016/j.jprot.2014.04.035
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Although the primary physiological effects produced by scorpion toxins are already well known, most of the secondary molecular events following scorpion neurotoxins-ion channel interactions are poorly understood and described. For this reason, we used a proteomic approach to determine the changes in relative protein abundance in F11 mouse neuroblastoma cells treated with Cn2, the major beta-toxin from the venom of the scorpion Centruroides noxius Hoffmann. Here we show that the relative abundance of 24 proteins changed after Cn2 treatment. Proteins related to protection from apoptosis and cell survival, as well as those involved in cell morphology and some translation elongation factors were diminished. By contrast, proteins associated with energy metabolism were increased. Additionally, results of western immunoblots confirmed the preference of action towards some special targets. These results suggest that Cn2 could modify the neuronal structure and induce apoptosis and reduction of the proliferation and cell survival. To support this conclusion we directly measured the Cn2 effect on cell proliferation, division and apoptosis. Our results open new avenues for continuing the studies aimed at better understanding the envenomation process caused by scorpion stings. Biological significance The purpose of this work was to identify which proteins, apart from the ion-channels, are involved in the envenomation process in order to develop possible strategies to circumvent the deleterious effects caused by the toxic peptides of the venom. For this reason, we characterized the early changes in the proteome of F11 cells induced by Cn2, the major toxin of the New World scorpion C. noxius Hoffmann, using 2D-PAGE and LC-MS/MS. We identified 24 proteins which relative abundance is modified after the Cn2 treatment. Among these, proteins related with apoptosis protection, cell survival, neuronal morphology and some translation elongation factors were diminished, whereas proteins associated with energy metabolism were increased. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:212 / 223
页数:12
相关论文
共 42 条
  • [1] On the mechanism of action of the scorpion toxin Cn2 on rSkm1 Na+ channels.
    Gómez-Lagunas, F
    Ramírez-Dominguez, ME
    Gurrola, G
    Possani, LD
    Kallen, RG
    [J]. BIOPHYSICAL JOURNAL, 2000, 78 (01) : 87A - 87A
  • [2] An NMR conformational analysis of a synthetic peptide Cn2(1-15)NH2S-S-acetyl-Cn2(52-66)NH2 from the New World Centruroides noxius 2 (Cn2) scorpion toxin:: Comparison of the structure with those of the Centruroides scorpion toxins
    Yamamoto, H
    Sejbal, J
    York, E
    Stewart, JM
    Possani, LD
    Kotovych, G
    [J]. BIOPOLYMERS, 1999, 49 (04) : 277 - 286
  • [3] Analysis of the immune response induced by a scorpion venom sub-fraction, a pure peptide and a recombinant peptide, against toxin Cn2 of Centruroides noxius Hoffmann
    Garcia, C
    Calderón-Aranda, ES
    Anguiano, GAV
    Becerril, B
    Possani, LD
    [J]. TOXICON, 2003, 41 (04) : 417 - 427
  • [4] Mapping of an epitope recognized by a neutralizing monoclonal antibody specific to toxin Cn2 from the scorpion Centruroides noxius, using discontinuous synthetic peptides
    Calderon-Aranda, ES
    Selisko, B
    York, EJ
    Gurrola, GB
    Stewart, JM
    Possani, LD
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1999, 264 (03): : 746 - 755
  • [5] The E15R Point Mutation in Scorpion Toxin Cn2 Uncouples Its Depressant and Excitatory Activities on Human Nav1.6
    Israel, Mathilde R.
    Thongyoo, Panumart
    Deuis, Jennifer R.
    Craik, David J.
    Vetter, Irina
    Durek, Thomas
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2018, 61 (04) : 1730 - 1736
  • [6] EFFECTS OF A SCORPION TOXIN FROM ANDROCTONUS-AUSTRALIS VENOM ON ACTION POTENTIAL OF NEUROBLASTOMA-CELLS IN CULTURE
    BERNARD, P
    COURAUD, F
    LISSITZKY, S
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1977, 77 (02) : 782 - 788
  • [7] Potential of peptides selected from random phage-displayed libraries to mimic conformational epitopes:: A study on scorpion toxin Cn2 and the neutralizing monoclonal antibody BCF2
    Gazarian, TG
    Selisko, B
    Gurrola, GB
    Hernández, R
    Possani, LD
    Gazarian, KG
    [J]. COMBINATORIAL CHEMISTRY & HIGH THROUGHPUT SCREENING, 2003, 6 (02) : 119 - 132
  • [8] Directed evolution, phage display and combination of evolved mutants:: A strategy to recover the neutralization properties of the scFv version of BCF2 a neutralizing monoclonal antibody specific to scorpion toxin Cn2
    Juárez-González, VR
    Riaño-Umbarila, L
    Quintero-Hernández, V
    Olamendi-Portugal, T
    Ortiz-León, M
    Ortíz, E
    Possan, LD
    Becerril, B
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 2005, 346 (05) : 1287 - 1297
  • [9] Antibody BCF2 against scorpion toxin Cn2 from Centruroides noxius Hoffmann:: Primary structure and three-dimensional model as free Fv fragment and complexed with its antigen
    Selisko, B
    Licea, AF
    Becerril, B
    Zamudio, F
    Possani, LD
    Horjales, E
    [J]. PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS, 1999, 37 (01) : 130 - 143
  • [10] Quantitative proteomic analysis reveals the neuroprotective effects of huperzine A for amyloid beta treated neuroblastoma N2a cells
    Tao, Yimin
    Fang, Li
    Yang, Yiming
    Jiang, Hualiang
    Yang, Huaiyu
    Zhang, Haiyan
    Zhou, Hu
    [J]. PROTEOMICS, 2013, 13 (08) : 1314 - 1324