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Proteomic characterization of lipids rafts markers from the rat intestinal brush border

  1. Author:
    Nguyen, H. T. T.
    Amine, A. B.
    Lafitte, D.
    Waheed, A. A.
    Nicoletti, C.
    Villard, C.
    Letisse, M.
    Deyris, V.
    Roziere, M.
    Tchiakpe, L.
    Danielle, C. D.
    Comeau, L.
    Hiol, A.

  2. Author Address

    Univ Paul Cezanne, Fac Sci & Tech St Jerome, Inst Mediterraneen Rech Nutr, UMR INRA 1111,LCA LBBN, F-13397 Marseille 20, France. Univ Mediterranee, Fac Pharm, Lab Nutr & Dietet, Plateau Proteom UMR FRE 2727,27 Av J Moulin, F-13385 Marseille, France. Natl Canc Inst Frederick, HIV Drug Resistance Program, Virus Cell Interact Sect, Ft Detrick, MD 21702 USA Hiol, A, Univ Paul Cezanne, Fac Sci & Tech St Jerome, Inst Mediterraneen Rech Nutr, UMR INRA 1111,LCA LBBN, F-13397 Marseille 20, France
    1. Year: 2006
    2. Date: MAR 31
  2. Journal: Biochemical and Biophysical Research Communications
    1. 342
    2. 1
    3. Pages: 236-244
  4. Type of Article: Article
  1. Abstract:

    To assess intestinal lipid rafts functions through the characterization of their protein markers, we have isolated lipid rafts of rat mucosa either from the total membrane or purified brush-border membrane (BBM) by sucrose gradient fractionation after detergent treatment. In both membrane preparations, the floating fractions (4-5) were enriched in cholesterol, ganglioside GM1, and N aminopeptidase (NAP) known as intestinal lipid rafts markers. Based on MALDI-TOF/MS identification and simultaneous detection by immunoblotting, 12 proteins from BBM cleared from contaminants were selected as rafts markers. These proteins include several signaling/trafficking proteins belonging to the G protein family and the annexins as well as GPI-anchored proteins. Remarkably GP2, previously described as the pancreatic granule GPI-anchored protein, was found in intestinal lipid rafts. The proteomic strategy assayed on the intestine leads to the characterization of known (NAP, alkaline phosphatase, dipeptidyl aminopeptidase, annexin II, and galectin-4) and new (GP2, annexin IV, XIIIb, G alpha(q), G alpha(11), glutamate receptor, and GPCR 7) lipid rafts markers. Together our results indicate that some digestive enzymes, trafficking and signaling proteins may be functionally distributed in the intestine lipid rafts. (c) 2006 Elsevier Inc. All rights reserved

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External Sources

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  2. DOI: 10.1016/j.bbrc.2006.01.141
  3. View record in Web of Science®
  4. WOS: 000235793800032

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