Literature DB >> 8233611

Glutamate rich Plasmodium falciparum antigen (GLURP).

B Høgh1, R Thompson, I S Zakiuddin, C Boudin, M Borre.   

Abstract

We have characterized a glutamate rich Plasmodium falciparum antigen, GLURP, which by immunoassays appears to be present in both the pre-erythrocytic and erythrocytic stages of the vertebrate life cycle. The gene, which is located on chromosome 10, encodes a polypeptide of 1271 residues with a predicted molecular mass of 145 kDa. Rabbit antiserum against a fusion protein expressing the C-terminal end of the molecule detects a protein with a molecular mass of 220 kDa. The sequence includes two hydrophobic regions: one consisting of 23 residues and located by the N-terminus which may act as signal peptide, and the second located at the C-terminus consisting of 33 predominantly hydrophobic residues. Except for these hydrophobic regions the protein is hydrophilic and highly charged. The sequence has two tandem repeats designated as R1 and R2. These regions were found to be conserved in isolates from different geographical areas. High levels of anti-GLURP antibodies have been shown to correlate with low parasite density. The indication of GLURP being present in all stages of the parasite in the human host raises significantly the prospects of the potential of this molecule.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8233611

Source DB:  PubMed          Journal:  Parassitologia        ISSN: 0048-2951


  7 in total

1.  Cytophilic immunoglobulin responses to Plasmodium falciparum glutamate-rich protein are correlated with protection against clinical malaria in Dielmo, Senegal.

Authors:  C Oeuvray; M Theisen; C Rogier; J F Trape; S Jepsen; P Druilhe
Journal:  Infect Immun       Date:  2000-05       Impact factor: 3.441

2.  Immune responses to band 3 neoantigens on Plasmodium falciparum-infected erythrocytes in subjects living in an area of intense malaria transmission are associated with low parasite density and high hematocrit value.

Authors:  B Hogh; E Petersen; I Crandall; A Gottschau; I W Sherman
Journal:  Infect Immun       Date:  1994-10       Impact factor: 3.441

3.  Size and sequence polymorphisms in the glutamate-rich protein gene of the human malaria parasite Plasmodium falciparum in Thailand.

Authors:  Sittiporn Pattaradilokrat; Chawinya Trakoolsoontorn; Phumin Simpalipan; Natapot Warrit; Morakot Kaewthamasorn; Pongchai Harnyuttanakorn
Journal:  Parasit Vectors       Date:  2018-01-22       Impact factor: 3.876

4.  Low-Complexity Repetitive Epitopes of Plasmodium falciparum Are Decoys for Humoural Immune Responses.

Authors:  Nan Hou; Ning Jiang; Yu Ma; Yang Zou; Xianyu Piao; Shuai Liu; Qijun Chen
Journal:  Front Immunol       Date:  2020-04-15       Impact factor: 7.561

5.  Temporal dynamics of Plasmodium falciparum population in Metehara, east-central Ethiopia.

Authors:  Abeba Gebretsadik Reda; Alebachew Messele; Hussein Mohammed; Ashenafi Assefa; Lemu Golassa; Hassen Mamo
Journal:  Malar J       Date:  2022-09-15       Impact factor: 3.469

Review 6.  Merozoite surface proteins in red blood cell invasion, immunity and vaccines against malaria.

Authors:  James G Beeson; Damien R Drew; Michelle J Boyle; Gaoqian Feng; Freya J I Fowkes; Jack S Richards
Journal:  FEMS Microbiol Rev       Date:  2016-01-31       Impact factor: 16.408

7.  Antibody responses to P. falciparum blood stage antigens and incidence of clinical malaria in children living in endemic area in Burkina Faso.

Authors:  Mariama K Cherif; Oumarou Ouédraogo; Guillaume S Sanou; Amidou Diarra; Alphonse Ouédraogo; Alfred Tiono; David R Cavanagh; Theisen Michael; Amadou T Konaté; Nora L Watson; Megan Sanza; Tina J T Dube; Sodiomon B Sirima; Issa Nebié
Journal:  BMC Res Notes       Date:  2017-09-08
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.