Literature DB >> 6801031

Characteristics of the release of the surface coat protein from bloodstream forms of Trypanosoma brucei.

H P Voorheis, D J Bowles, G A Smith.   

Abstract

Bloodstream forms of the African trypanosomes undergo antigenic variation in their mammalian host. This process involves removal of the existing variant coat protein and its replacement with another. The mechanism by which the surface coat protein is released to the external supporting medium has been shown to depend in vitro specifically on the presence of calcium ions together with the calcium ionophore. A-23187, and to be inhibited by Zn2+. Release of the surface coat protein was not stimulated by conditions designed to alter the plasma membrane potential or the major ionic gradients across that membrane. Release could be stimulated by inhibiting the energy metabolism of these glycolysing cells with 2-deoxyglucose, which probably prevents the energy-dependent mechanisms that normally keep the cytoplasmic Ca2+ concentration low. These results and the finding that the release process was strongly temperature dependent suggested the possible mediation of some as yet undefined enzymatic reaction.

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Year:  1982        PMID: 6801031

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  9 in total

1.  A novel selection regime for differentiation defects demonstrates an essential role for the stumpy form in the life cycle of the African trypanosome.

Authors:  M Tasker; J Wilson; M Sarkar; E Hendriks; K Matthews
Journal:  Mol Biol Cell       Date:  2000-05       Impact factor: 4.138

2.  Ca2+ signaling in the transformation of promastigotes to axenic amastigotes of Leishmania donovani.

Authors:  A Prasad; S Kaur; N Malla; N K Ganguly; R C Mahajan
Journal:  Mol Cell Biochem       Date:  2001-08       Impact factor: 3.396

3.  A new method for the rapid purification of both the membrane-bound and released forms of the variant surface glycoprotein from Trypanosoma brucei.

Authors:  D G Jackson; M J Owen; H P Voorheis
Journal:  Biochem J       Date:  1985-08-15       Impact factor: 3.857

4.  A gene from the variant surface glycoprotein expression site encodes one of several transmembrane adenylate cyclases located on the flagellum of Trypanosoma brucei.

Authors:  P Paindavoine; S Rolin; S Van Assel; M Geuskens; J C Jauniaux; C Dinsart; G Huet; E Pays
Journal:  Mol Cell Biol       Date:  1992-03       Impact factor: 4.272

5.  Studies on compounds promoting the in vitro transformation of Trypanosoma brucei from bloodstream to procyclic forms.

Authors:  M Hunt; R Brun; P Köhler
Journal:  Parasitol Res       Date:  1994       Impact factor: 2.289

6.  A calmodulin-activated (Ca(2+)-Mg2+)-ATPase is involved in Ca2+ transport by plasma membrane vesicles from Trypanosoma cruzi.

Authors:  G Benaim; S Losada; F R Gadelha; R Docampo
Journal:  Biochem J       Date:  1991-12-15       Impact factor: 3.857

7.  The GPI-phospholipase C of Trypanosoma brucei is nonessential but influences parasitemia in mice.

Authors:  H Webb; N Carnall; L Vanhamme; S Rolin; J Van Den Abbeele; S Welburn; E Pays; M Carrington
Journal:  J Cell Biol       Date:  1997-10-06       Impact factor: 10.539

Review 8.  Disruption of Intracellular Calcium Homeostasis as a Therapeutic Target Against Trypanosoma cruzi.

Authors:  Gustavo Benaim; Alberto E Paniz-Mondolfi; Emilia Mia Sordillo; Nathalia Martinez-Sotillo
Journal:  Front Cell Infect Microbiol       Date:  2020-02-14       Impact factor: 5.293

9.  The glycosylphosphatidylinositol-PLC in Trypanosoma brucei forms a linear array on the exterior of the flagellar membrane before and after activation.

Authors:  Orla Hanrahan; Helena Webb; Robert O'Byrne; Elaine Brabazon; Achim Treumann; Jack D Sunter; Mark Carrington; H Paul Voorheis
Journal:  PLoS Pathog       Date:  2009-06-05       Impact factor: 6.823

  9 in total

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