4.5 Article

Ato protein interactions in yeast plasma membrane revealed by fluorescence lifetime imaging (FLIM)

Journal

BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES
Volume 1818, Issue 9, Pages 2126-2134

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.bbamem.2012.05.005

Keywords

Ammonium exporters Ato1p, Ato2p and Ato3p; FLIM-photobleaching technique; Homo/hetero di(oligo)mers; Plasma membrane protein interaction; Donor lifetime

Funding

  1. Grant Agency of the Czech Republic [204/08/0718]
  2. Ministry of Education [LC06063, LC531, MSM0021620858]
  3. GAUK [261214]
  4. UNCE [204013]
  5. RVO [61388971]
  6. Howard Hughes Medical Institute International Research Award [55005623]

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Each of the three plasma membrane Ato proteins is involved in ammonium signalling and the development of yeast colonies. This suggests that although these proteins are homologous, they do not functionally substitute for each other, but may form a functional complex. Here, we present a detailed combined FRET, FLIM and photobleaching study, which enabled us to detect interactions between Ato proteins found in distinct compartments of yeast cells. We thus show that the proteins Ato1p and Ato2p interact and can form complexes when present in the plasma membrane. No interaction was detected between Ato1p and Ato3p or Ato2p and Ato3p. In addition, using specially prepared strains, we were able to detect an interaction between molecules of the same Ato protein, namely Ato1p-Ato1p and Ato3p-Ato3p, but not Ato2p-Ato2p. (C) 2012 Elsevier B.V. All rights reserved.

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