Plasmodium chabaudi: Expression of active recombinant chabaupain-1 and localization studies in Anopheles sp.

被引:15
作者
Caldeira, Rubina L.
Goncalves, Lidia M. D. [3 ,4 ]
Martins, Tiago M.
Silveira, Henrique [2 ]
Novo, Carlos [2 ]
do Rosario, Virgilio [2 ]
Domingos, Ana [1 ,2 ]
机构
[1] INETI Natl Inst Engn Technol & Innovat, Dept Biotechnol, Unit Prot & Monoclonal Antidody Technol, UTPAM, P-1649038 Lisbon, Portugal
[2] IHMT CMDT Inst Hyg & Trop Med, Ctr Malaria & Trop Dis, P-1349008 Lisbon, Portugal
[3] IBET Inst Biol Expt & Tecnol, P-2780901 Oeiras, Portugal
[4] Univ Lisbon, Fac Farm, IMed UL Res Inst Med & Pharmaceut Sci, P-1649003 Lisbon, Portugal
关键词
Malaria; Plasmodium chabaudi; Recombinant cysteine proteases; Chabaupain; FALCIPARUM CYSTEINE PROTEASE; HEMOGLOBIN DEGRADATION; MALARIA; PROTEINASE; INHIBITION; DISRUPTION; ANTIBODY; PEPTIDE; CLONING; MICE;
D O I
10.1016/j.exppara.2009.03.003
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Plasmodium cysteine proteases have been shown to be immunogenic and are being used as malaria potential serodiagnostic markers and vaccine targets. Genes encoding two Plasmodium chabaudi cysteine proteases chabaupain-1 (CP-1) and chabaupain-2 (CP-2) were identified and further expressed in Escherichia coli. Solubilisation of recombinant CP-1 and CP-2 was achieved by decreasing the temperature of induction. Anopheles gambiae tissues infected with Plasmodium were analyzed by Western blotting using the anti-CP-1 antibody showing that CP-1 is only present in the A. gambiae midguts being absent from other infected mosquito biological material. Anti-CP-1 anti-serum recognized a 30 kDa band in P. chabaudi, Plasmodium berghei and Plasmodium yoelii lysates but does not recognize the recombinant CP-2 extracts suggesting high antibody specificity. (c) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:97 / 105
页数:9
相关论文
共 36 条
  • [1] A malarial cysteine protease is necessary for Plasmodium sporozoite egress from oocysts
    Aly, ASI
    Matuschewski, K
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 202 (02) : 225 - 230
  • [2] Of mice and malaria mutants: unravelling the genetics of drug resistance using rodent malaria models
    Carlton, JMR
    Hayton, M
    Cravo, PVL
    Walliker, D
    [J]. TRENDS IN PARASITOLOGY, 2001, 17 (05) : 236 - 242
  • [3] Gene synteny in species of Plasmodium
    Carlton, JMR
    Vinkenoog, R
    Waters, AP
    Walliker, D
    [J]. MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1998, 93 (02) : 285 - 294
  • [4] Monoclonal antibody MG96 completely blocks Plasmodium yoelii development in Anopheles stephensi
    Dinglasan, RR
    Fields, I
    Shahabuddin, M
    Azad, AF
    Sacci, JB
    [J]. INFECTION AND IMMUNITY, 2003, 71 (12) : 6995 - 7001
  • [5] DOWSE TJ, 2008, SUBCELLULAR BIOCH, V9, P47
  • [6] Targeted disruption of Plasmodium falciparum cysteine protease, falcipain 1, reduces oocyst production, not erythrocytic stage growth
    Eksi, S
    Czesny, B
    Greenbaum, DC
    Bogyo, M
    Williamson, KC
    [J]. MOLECULAR MICROBIOLOGY, 2004, 53 (01) : 243 - 250
  • [7] HEMOGLOBIN DEGRADATION IN THE MALARIA PARASITE PLASMODIUM-FALCIPARUM - AN ORDERED PROCESS IN A UNIQUE ORGANELLE
    GOLDBERG, DE
    SLATER, AFG
    CERAMI, A
    HENDERSON, GB
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (08) : 2931 - 2935
  • [8] A role for the protease falcipain 1 in host cell invasion by the human malaria parasite
    Greenbaum, DC
    Baruch, A
    Grainger, M
    Bozdech, Z
    Medzihradszky, KF
    Engel, J
    DeRisi, J
    Holder, AA
    Bogyo, M
    [J]. SCIENCE, 2002, 298 (5600) : 2002 - 2006
  • [9] Malaria
    Greenwood, BM
    Bojang, K
    Whitty, CJM
    Targett, GAT
    [J]. LANCET, 2005, 365 (9469) : 1487 - 1498
  • [10] Hall T.A., 1999, NUCL ACIDS S SER, V41, P95