A photoreactive derivative of radiolabeled GM1 ganglioside: preparation and use to establish the involvement of specific proteins in GM1 uptake by human fibroblasts in culture

• Published in: Biochemistry (Easton) Vol. 28; no. 1; pp. 77 - 84
• Main Authors: Sonnino, Sandro, Chigorno, Vanna, Acquotti, Domenico, Pitto, Marina, Kirschner, Gunther, Tettamanti, Guido
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 10.01.1989
• Subjects: 550201 - Biochemistry- Tracer Techniques; ANIMAL CELLS; ANIMALS; AZIDES; BARYONS; BASIC BIOLOGICAL SCIENCES; BIOELECTRICITY; Biological Transport, Active; CARBOHYDRATES; Carrier Proteins - metabolism; CELL CONSTITUENTS; CELL CULTURES; Cell Membrane - metabolism; CELL MEMBRANES; Cells, Cultured; CHEMICAL REACTIONS; CONNECTIVE TISSUE CELLS; CROSS-LINKING; DERIVATIZATION; ELECTRICITY; ELECTROPHORESIS; ELEMENTARY PARTICLES; FERMIONS; FIBROBLASTS; Fibroblasts - metabolism; G(M1) Ganglioside - analogs & derivatives; G(M1) Ganglioside - chemical synthesis; G(M1) Ganglioside - metabolism; GANGLIOSIDES; GLYCOLIPIDS; HADRONS; HEAVY WATER; Humans; HYDROGEN COMPOUNDS; LABELLING; LIPIDS; MAGNETIC RESONANCE; MAMMALS; MAN; Membrane Lipids - metabolism; Membrane Proteins - metabolism; MEMBRANES; NITRO COMPOUNDS; NITROGEN COMPOUNDS; NMR SPECTRA; NUCLEAR MAGNETIC RESONANCE; NUCLEONS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; OXYGEN COMPOUNDS; Photochemistry; POLYMERIZATION; PRIMATES; PROTEINS; PROTONS; RESONANCE; SACCHARIDES; SOMATIC CELLS; SPECTRA; TRITIUM COMPOUNDS; VERTEBRATES; WATER
• ISSN: 0006-2960; 1520-4995
• DOI: 10.1021/bi00427a012

A new procedure was used to synthesize a derivative of ganglioside GM1 containing a photoreactive nitrophenyl azide group at the end of the fatty acyl moiety, using deAc-deAcyl-GM1 obtained by deacetylation of the sialic acid and deacylation of the ceramide portion of GM1. This deAc-deAcyl-GM1 was first acylated at the long chain base amino group with 12-aminododecanoic acid, which has the amino group protected by a fluorenyl residue, and tritium labeled at the sialic acid amino group with [3H]acetic anhydride of very high specific radioactivity. The fluorenyl group removed by ammonia treatment was substituted by a nitrophenyl azide group. Cultured human fibroblasts were exposed to mixtures of radioactive photolabeled GM1 and cold natural GM1 (1:10 by mol) for different times and then illuminated and the radioactive protein patterns studied by SDS-PAGE. After 2h of exposure, the photolabeled GM1 was stably associated to the cells and underwent almost no metabolic processing, behaving exactly as the underivatized natural GM1. Under these conditions very few proteins became radioactive: one, of about 30 kDa, interacted with the ganglioside molecules inserted into the outer membrane layer; three, in the region of 46 kDa, interacted with the portion of associated ganglioside able to be released by trypsin treatment. Thus, it is evident that the ganglioside binding to fibroblasts and insertion into the outer layer of the plasma membrane involve few individual proteins.