Plasmodium vivax merozoite surface proteins-3β and-3γ share structural similarities with P. vivax merozoite surface protein-3α and define a new gene family

被引:58
作者
Galinski, MR
Ingravallo, P
Corredor-Medina, C
Al-Khedery, B
Povoa, M
Barnwell, JW
机构
[1] Emory Univ, Dept Med, Emory Vaccine Res Ctr, Yerkes Primate Res Ctr, Atlanta, GA 30329 USA
[2] NYU, Sch Med, New York, NY 10010 USA
[3] Inst Evandros Chagas, Belem, Para, Brazil
[4] Ctr Dis Control & Prevent, Div Parasit Dis, Atlanta, GA 30341 USA
关键词
Plasmodium vivax; malaria; merozoite; vaccine; surface protein; coiled-coils;
D O I
10.1016/S0166-6851(01)00267-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The genes encoding two merozoite surface proteins of Plasmodium vivax that are related to PvMSP3 [1] are reported. One of these genes was identified within P. vivax, lambda gt11 clone 5.4, which was selected by immunoscreening with a Saimiri monkey antiserum. The insert DNA of this clone was used as a probe to isolate the complete gene from a P. vivax lambda DASH genomic (g) DNA library. Antibodies to recombinant 5.4 and subsequent fusion proteins produce a pattern of circumferential surface fluorescence by indirect immunofluorescence assays (IFA) on segmented schizonts and free intact merozoites, and recognize a 125 kDa protein via western immunoblots. The gene, however, encodes a protein with a calculated size of 75 677 Da, and 3 ' and 5 ' RACE analyses were employed to confirm the size of the gene and its coding region. The second related P. vivax gene was isolated by hybridization of a fragment of an orthologous P. knowlesi gene. The encoded proteins of all three related P. vivax genes have putative signal peptides, large central domains that contain > 20% alanine residues bound by charged regions, are predicted to form alpha -helices with heptad repeat coiled-coil structures, and do not have a hydrophobic region that could anchor them to the surface of the merozoite. Although the overall identity in amino acid alignment among the three encoded proteins is low ( < 40%) the shared predicted structural features and motifs indicate that they are members of an intra-species family, which we are designating as the PvMSP-3 family with the reported members being Pvmsp-3 alpha, Pvmsp-3 beta, and Pvmsp-3 gamma. We further demonstrate that this family also includes related proteins from P, knowlesi and P. falciparum. (C) 2001 Elsevier Science B.V. All rights reserved.
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页码:41 / 53
页数:13
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