Parasitology Research

, Volume 87, Issue 2, pp 112–115 | Cite as

Characterization of a proteasome α-chain from Giardia lamblia

  • Vera Emmerlich
  • Henning Scholze
  • Frances D. Gillin
  • Tilly Bakker-Grunwald
ORIGINAL PAPER

Abstract

To begin to characterize the components of the 20S proteasome of Giardia lamblia, we have cloned a genomic sequence encoding an α-chain (type α3/C9, predicted size 244 amino acid residues). Southern analysis indicated that a single gene codes for this protein, and a Northern blot exhibited a single signal at 850 nt. An antiserum against a C-terminal fragment of the α-chain expressed in Escherichia coli reacted with a single protein band of Mr 27,000 that was present at constant levels in trophozoites and encysting cells. On a 2D blot of the purified 20S proteasome, we identified the crossreacting component as a single protein of IEP 6.0, in agreement with the IEP predicted by the coding sequence. Our data confirm that the G. lamblia 20S proteasome is typically eukaryotic in containing a set of diverged α-subunits.

Keywords

Escherichia Coli Genomic Sequence Amino Acid Residue Northern Blot Single Gene 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Springer-Verlag Berlin Heidelberg 2001

Authors and Affiliations

  • Vera Emmerlich
    • 1
  • Henning Scholze
    • 2
  • Frances D. Gillin
    • 3
  • Tilly Bakker-Grunwald
    • 1
  1. 1.Department of Microbiology, University of Osnabrück, Barbarastrasse 11, 49069 Osnabrück, Germany e-mail: bakker_t@biologie.uni-osnabrueck.de Tel.: +49-541-9692796; Fax: +49-541-9692870DE
  2. 2.Department of Biochemistry, University of Osnabrück, 49069 Osnabrück, GermanyDE
  3. 3.Department of Pathology and Center for Molecular Genetics, University of California at San Diego Medical School, San Diego, CA 92103-8416, USAUS

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