RESUMEN
Citrus pectin is known to influence carotenoid bioaccessibility and absorption in humans, but limited attention has been given to the influence of pectin structure related to the particle size from differentially processed citrus food matrices. In this context, this study aims to investigate the nutritional health benefits of an innovative Citrus clementina concentrate, which is a new citrus-based food made by cross-flow microfiltration. This concentrated citrus-based food was selectively enriched 8-fold in ß-cryptoxanthin (43-55 µg g-1) and ß-carotene (6-9 µg g-1) as well as 6-fold in pectin (376-462 mg per 100 g). The bioaccessibility of pro-vitamin A carotenoids from commercial and fresh clementina juices versus their concentrates was assessed, including the intestinal carotenoid uptake by Caco-2 cells. Differences in particles size and pectin status resulted in a 7-fold increase in the bioaccessibility of carotenoids in industrial products versus fresh products while limiting their cellular uptake in correlation with larger micelle sizes (10.6 nm and 6.82 nm for industrial and fresh concentrates, respectively). Overall, the highest carotenoid bioaccessibility from industrial concentrate was sufficient to offset the lower carotenoid intestinal uptake related to micelle size. This study highlights that the structure of pectins, more specifically their degree of methoxylation, favors carotenoid bioaccessibility but impairs the intestinal absorption of carotenoids from citrus concentrates.
Asunto(s)
Jugos de Frutas y Vegetales/análisis , Mucosa Intestinal/metabolismo , Pectinas/química , beta-Criptoxantina/metabolismo , Células CACO-2 , Citrus/química , Citrus/metabolismo , Digestión , Humanos , Tamaño de la Partícula , Pectinas/metabolismo , beta Caroteno/metabolismoRESUMEN
The metabolic effects of an oral supplementation with a Curcuma longa extract, at a dose nutritionally relevant with common human use, on hepatic metabolism in rats fed a high fructose and saturated fatty acid (HFS) diet was evaluated. High-resolution magic-angle spinning NMR and GC/MS in combination with multivariate analysis have been employed to characterize the NMR metabolite profiles and fatty acid composition of liver tissue respectively. The results showed a clear discrimination between HFS groups and controls involving metabolites such as glucose, glycogen, amino acids, acetate, choline, lysophosphatidylcholine, phosphatidylethanolamine, and ß-hydroxybutyrate as well as an increase of MUFAs and a decrease of n-6 and n-3 PUFAs. Although the administration of CL did not counteract deleterious effects of the HFS diet, some metabolites, namely some n-6 PUFA and n-3 PUFA, and betaine were found to increase significantly in liver samples from rats having received extract of curcuma compared to those fed the HFS diet alone. This result suggests that curcuminoids may affect the transmethylation pathway and/or osmotic regulation. CL extract supplementation in rats appears to increase some of the natural defences preventing the development of fatty liver by acting on the choline metabolism to increase fat export from the liver.
Asunto(s)
Suplementos Dietéticos , Hígado/metabolismo , Extractos Vegetales/farmacología , Animales , Betaína/metabolismo , Colina/metabolismo , Curcuma , Dieta Alta en Grasa , Análisis Discriminante , Ácidos Grasos , Fructosa , Glutatión/metabolismo , Análisis de los Mínimos Cuadrados , Masculino , Malondialdehído/metabolismo , Análisis Multivariante , Espectroscopía de Protones por Resonancia Magnética , Ratas Sprague-Dawley , Triglicéridos/metabolismoRESUMEN
We explored, using nuclear magnetic resonance (NMR) metabolomics and fatty acids profiling, the effects of a common nutritional complement, Curcuma longa, at a nutritionally relevant dose with human use, administered in conjunction with an unbalanced diet. Indeed, traditional food supplements have been long used to counter metabolic impairments induced by unbalanced diets. Here, rats were fed either a standard diet, a high level of fructose and saturated fatty acid (HFS) diet, a diet common to western countries and that certainly contributes to the epidemic of insulin resistance (IR) syndrome, or a HFS diet with a Curcuma longa extract (1% of curcuminoids in the extract) for ten weeks. Orthogonal projections to latent structures discriminant analysis (OPLS-DA) on the serum NMR profiles and fatty acid composition (determined by GC/MS) showed a clear discrimination between HFS groups and controls. This discrimination involved metabolites such as glucose, amino acids, pyruvate, creatine, phosphocholine/glycerophosphocholine, ketone bodies and glycoproteins as well as an increase of monounsaturated fatty acids (MUFAs) and a decrease of n-6 and n-3 polyunsaturated fatty acids (PUFAs). Although the administration of Curcuma longa did not prevent the observed increase of glucose, triglycerides, cholesterol and insulin levels, discriminating metabolites were observed between groups fed HFS alone or with addition of a Curcuma longa extract, namely some MUFA and n-3 PUFA, glycoproteins, glutamine, and methanol, suggesting that curcuminoids may act respectively on the fatty acid metabolism, the hexosamine biosynthesis pathway and alcohol oxidation. Curcuma longa extract supplementation appears to be beneficial in these metabolic pathways in rats. This metabolomic approach highlights important serum metabolites that could help in understanding further the metabolic mechanisms leading to IR.
Asunto(s)
Curcuma/metabolismo , Ácidos Grasos/farmacología , Jarabe de Maíz Alto en Fructosa/farmacología , Redes y Vías Metabólicas/fisiología , Extractos Vegetales/farmacología , Animales , Antioxidantes/metabolismo , Análisis Químico de la Sangre , Glucemia/análisis , Colesterol/sangre , Dieta , Grasas de la Dieta , Suplementos Dietéticos , Ácidos Grasos/administración & dosificación , Ácidos Grasos/sangre , Fructosa/administración & dosificación , Jarabe de Maíz Alto en Fructosa/administración & dosificación , Insulina/sangre , Metabolismo de los Lípidos/efectos de los fármacos , Lípidos/sangre , Espectroscopía de Resonancia Magnética , Masculino , Redes y Vías Metabólicas/efectos de los fármacos , Metabolómica , Estrés Oxidativo/fisiología , Extractos Vegetales/administración & dosificación , Ratas , Ratas Sprague-Dawley , Triglicéridos/sangreRESUMEN
In the tropics one of the major constraints to goat production is infection by gastrointestinal nematodes (GIN). One promising alternative to chemotherapy is the improvement of host nutrition. The aim of this study was to assess the effects of infection and supplementation on packed cell volume (PCV), average daily gain (ADG) and carcass quality in growing Creole kids. Sixty male goats were reared indoors following a 2 × 3 factorial design: two experimental infection levels, (infected (I) and non-infected (NI)) and three diets D (G, kids were fed exclusively with tropical forages; B, kids were supplemented with dried and crushed banana and C, kids were supplemented with commercial pellets). Faecal egg counts did not vary among I groups (on average 2,200 ω/g). The PCV and ADG were improved (P < 0.001) for NI vs. I animals. There was a D effect (P < 0.001) and no I × D interaction was observed. There was no significant effect of GIN on the main carcass data, except the weights of liver, white offal and abdominal fat, which increased slightly in I compared with NI goats (P < 0.05). All carcass data increased significantly with the addition of supplement in the diet (P < 0.001), except for carcass-cut proportions. Meat physical parameters were degraded when I kids received low N diets (B or G) with higher lightness and water loss than in the C groups. Given that GIN affect the animal's N metabolism it is recommended to avoid the use of unbalanced diet such as those banana-based. Further research is necessary to assess the nutrition × parasitism interactions on physiological features and carcass quality of Creole goats.
Asunto(s)
Composición Corporal , Dieta/veterinaria , Enfermedades Gastrointestinales/veterinaria , Enfermedades de las Cabras/fisiopatología , Infecciones por Nematodos/veterinaria , Fenómenos Fisiológicos Nutricionales de los Animales , Animales , Animales Recién Nacidos/crecimiento & desarrollo , Suplementos Dietéticos , Heces/parasitología , Enfermedades Gastrointestinales/parasitología , Enfermedades Gastrointestinales/fisiopatología , Enfermedades de las Cabras/parasitología , Cabras , Masculino , Carne , Nematodos/aislamiento & purificación , Infecciones por Nematodos/parasitología , Infecciones por Nematodos/fisiopatología , Recuento de Huevos de Parásitos/veterinaria , Aumento de Peso/fisiologíaRESUMEN
The combined influence of maturation, ripening, and climate on the profile of bioactive compounds was studied in banana (Musa acuminata, AAA, Cavendish, cv. Grande Naine). Their bioactive compounds were determined by the Folin-Ciocalteu assay and high-performance thin layer chromatographic (HPTLC) method. The polyphenol content of bananas harvested after 400 degree days remained unchanged during ripening, while bananas harvested after 600 and 900 degree days exhibited a significant polyphenol increase. Although dopamine was the polyphenol with the highest concentration in banana peels during the green developmental stage and ripening, its kinetics differed from the total polyphenol profile. Our results showed that this matrix of choice (maturation, ripening, and climate) may allow selection of the banana (M. acuminata, AAA, Cavendish, cv. Grande Naine) status that will produce optimal concentrations of identified compounds with human health relevance.
Asunto(s)
Clima , Dopamina/análisis , Dopamina/metabolismo , Frutas/fisiología , Musa/fisiología , Polifenoles/análisis , Polifenoles/metabolismo , Análisis de los AlimentosRESUMEN
As the consumption of fructose and saturated fatty acids (FAs) has greatly increased in western diets and is linked with an increased risk of metabolic syndrome, the aim of this study was to investigate the effects of a moderate (10 weeks) and a prolonged (30 weeks) high fructose and saturated fatty acid (HFS) diet on plasma FA composition in rats. The effects of a few weeks of HFS diet had already been described, but in this paper we tried to establish whether these effects persist or if they are modified after 10 or 30 weeks. We hypothesized that the plasma FA profile would be altered between 10 and 30 weeks of the HFS diet. Rats fed with either the HFS or a standard diet were tested after 10 weeks and again after 30 weeks. After 10 weeks of feeding, HFS-fed rats developed the metabolic syndrome, as manifested by an increase in fasting insulinemia, total cholesterol and triglyceride levels, as well as by impaired glucose tolerance. Furthermore, the plasma FA profile of the HFS group showed higher proportions of monounsaturated FAs like palmitoleic acid [16:1(n-7)] and oleic acid [18:1(n-9)], whereas the proportions of some polyunsaturated n-6 FAs, such as linoleic acid [18:2(n-6)] and arachidonic acid [20:4(n-6)], were lower than those in the control group. After 30 weeks of the HFS diet, we observed changes mainly in the levels of 16:1(n-7) (decreased) and 20:4(n-6) (increased). Together, our results suggest that an HFS diet could lead to an adaptive response of the plasma FA profile over time, in association with the development of the metabolic syndrome.
Asunto(s)
Grasas de la Dieta/metabolismo , Sacarosa en la Dieta/metabolismo , Ácidos Grasos/sangre , Ácidos Grasos/metabolismo , Fructosa/metabolismo , Administración Oral , Animales , Ácidos Grasos/administración & dosificación , Fructosa/administración & dosificación , Masculino , Ratas , Ratas Sprague-DawleyRESUMEN
The transporter PepT1, apically expressed in intestinal epithelial cells, is responsible for the uptake of di/tripeptides. PepT1 is also expressed in nonpolarized immune cells. Here we investigated the localization of PepT1 in lipid rafts in small intestinal brush border membranes (BBMs) and polarized and nonpolarized cells, as well as functional consequences of the association of PepT1 with lipid rafts. Immunoblot analysis showed the presence of PepT1 in low-density fractions isolated from mouse intestinal BBMs, polarized intestinal Caco2-BBE cells, and nonpolarized Jurkat cells by solubilization in ice-cold 0.5% Triton X-100 and sucrose gradient fractionation. PepT1 colocalized with lipid raft markers GM1 and N-aminopeptidase in intestinal BBMs and Caco2-BBE cell membranes. Disruption of lipid rafts with methyl-beta-cyclodextrin (MbetaCD) shifted PepT1 from low- to high-density fractions. Remarkably, we found that MbetaCD treatment increased PepT1 transport activity in polarized intestinal epithelia but decreased that in intestinal BBM vesicles and nonpolarized immune cells. Mutational analysis showed that phenylalanine 293, phenylalanine 297, and threonine 281 in transmembrane segment 7 of the human di/tripeptide transporter, hPepT1, are important for the targeting to lipid rafts and transport activity of hPepT1. In conclusion, the association of PepT1 with lipid rafts differently modulates its transport activity in polarized and nonpolarized cells.
Asunto(s)
Mucosa Intestinal/citología , Mucosa Intestinal/metabolismo , Intestino Delgado/citología , Intestino Delgado/metabolismo , Transporte de Proteínas/fisiología , Simportadores/metabolismo , Animales , Transporte Biológico Activo/fisiología , Células CACO-2 , Polaridad Celular , Células Cultivadas , Humanos , Masculino , Ratones , Transportador de Péptidos 1RESUMEN
BACKGROUND: Action potentials are the classic mechanism by which neurons convey a state of excitation throughout their length, leading, after synaptic transmission, to the activation of other neurons and consequently to network functioning. Using an in vitro integrated model, we found previously that peripheral networks in the autonomic nervous system can organise an unconventional regulatory reflex of the digestive tract motility without action potentials. METHODOLOGY/PRINCIPAL FINDINGS: In this report, we used combined neuropharmacological and biochemical approaches to elucidate some steps of the mechanism that conveys excitation along the nerves fibres without action potentials. This mechanism requires the production of ceramide in membrane lipid rafts, which triggers in the cytoplasm an increase in intracellular calcium concentration, followed by activation of a neuronal nitric oxide synthase leading to local production of nitric oxide, and then to guanosine cyclic monophosphate. This sequence of second messengers is activated in cascade from rafts to rafts to ensure conduction of the excitation along the nerve fibres. CONCLUSIONS/SIGNIFICANCE: Our results indicate that second messengers are involved in neuronal conduction of excitation without action potentials. This mechanism represents the first evidence-to our knowledge-that excitation is carried along nerves independently of electrical signals. This unexpected ceramide-based conduction of excitation without action potentials along the autonomic nerve fibres opens up new prospects in our understanding of neuronal functioning.
Asunto(s)
Potenciales de Acción/fisiología , Ceramidas/biosíntesis , Duodeno/fisiología , Fibras Nerviosas/fisiología , Neuronas/fisiología , Sistemas de Mensajero Secundario/fisiología , Estómago/fisiología , Transmisión Sináptica/fisiología , Animales , GMP Cíclico/fisiología , Duodeno/inervación , Microdominios de Membrana/fisiología , Contracción Muscular , Músculo Liso/fisiología , Red Nerviosa/fisiología , Óxido Nítrico/fisiología , Ratas , Estómago/inervaciónRESUMEN
In the present work, we induced obesity in rats with high-energy-starch diet and studied exocrine pancreas response. The zymogen granule (ZG) or purified plasma membrane (PM) from the exocrine pancreas was used for the isolation of the detergent-resistant membranes (DRMs). Based on high content of cholesterol, GM1, the bile salt dependent lipase (BSDL), and GP2 enrichment, the low-density fractions were defined as lipid rafts. Additionally, the rafts vesicles were determined by immunogold labeling with anti BSDL. By combining MALDI-TOF/MS and nano-LC ESI Q-TOF MS/MS proteomic identification we have selected 33 proteins from the lipid rafts which were classified into at least four functional families. Our data suggest that the acinar PM from the diet-induced obesity rats may be organized into lipid rafts, and characterization of rafts proteome can contribute to improve our understanding of food digestion under obesity.
Asunto(s)
Membrana Celular/química , Microdominios de Membrana/química , Obesidad/metabolismo , Páncreas Exocrino/química , Proteómica , Animales , Membrana Celular/ultraestructura , Dieta , Masculino , Microdominios de Membrana/metabolismo , Páncreas Exocrino/metabolismo , Proteínas/análisis , Ratas , Ratas Sprague-DawleyRESUMEN
Sphingolipids are present in all eukaryotic cells and share a sphingoid base : sphingosine. They were first discovered in 1884 and for a long time they were thought to participate to membrane structure only. Recently it has been established that they are mainly located in particular areas of the membrane called rafts which are signalling platforms. It has also been demonstrated that sphingolipids are receptors and second messengers. They play a crucial role in cellular functioning and are necessary to maintenance and developing of living organisms. However due to their receptor properties, they are also gateway for penetration of pathogenic agents such as virus (Ebola, HIV) or toxins (botulinium, tetanus). These agents first bind to glycosphingolipids or proteins mainly located in rafts. The complex so formed is required for the crossing of the membrane by the pathogenic agent. Sphingolipids metabolism is regulated by numerous enzymes. A failure in the activity of one of them induces an accumulation of sphingolipids known as sphingolipidoses. These are genetic diseases having severe consequences for the survival of the organism. The precise mechanisms of the sphingolipidoses are still mainly unknown which explains why few therapeutic strategies are available. These particular properties of lipids rafts and sphingolipids explain why a growing number of studies in the medical and scientific fields are devoted to them.
Asunto(s)
Esfingolipidosis/metabolismo , Esfingolípidos/fisiología , Animales , Apoptosis/fisiología , Autoantígenos/inmunología , Enfermedades Autoinmunes/inmunología , Membrana Celular/ultraestructura , Membrana Celular/virología , Síndrome de Guillain-Barré/inmunología , Humanos , Lípidos de la Membrana/fisiología , Microdominios de Membrana , Neurotoxinas/farmacocinética , Ratas , Ratas Zucker , Receptores de Superficie Celular/genética , Receptores de Superficie Celular/fisiología , Receptores Virales/fisiología , Sistemas de Mensajero Secundario/fisiología , Esfingolipidosis/clasificación , Esfingolipidosis/genética , Esfingolípidos/inmunología , Esfingolípidos/metabolismoRESUMEN
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, Galpha(q), Galpha(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.
Asunto(s)
Intestinos/citología , Microdominios de Membrana/metabolismo , Microvellosidades/metabolismo , Proteómica , Animales , Anexina A2/clasificación , Anexina A2/metabolismo , Biomarcadores , Detergentes/farmacología , Proteínas Ligadas a GPI , Galectina 4/metabolismo , Glicosilfosfatidilinositoles/metabolismo , Guanidina/metabolismo , Masculino , Glicoproteínas de Membrana/metabolismo , Microdominios de Membrana/efectos de los fármacos , Microscopía Inmunoelectrónica , Microvellosidades/efectos de los fármacos , Fosfatidilinositol Diacilglicerol-Liasa/metabolismo , Ratas , Ratas Wistar , Espectrometría de Masa por Láser de Matriz Asistida de Ionización DesorciónRESUMEN
The acylation of proteins through the addition of palmitate to cysteine residues is a common posttranslational modification for a variety of proteins, but the enzymology of this reversible modification has resisted elucidation. We developed a strategy to purify protein fatty acyltransferase (PAT) activity from rat livers that took advantage of recent knowledge on the cellular location and inhibition of PAT activity. We determined that three different thiolases have PAT activity in the presence of imidazole and therefore started the purification with a plasma membrane fraction to minimize the contamination with these enzymes. After detergent extraction of the plasma membrane fraction, the PAT activity was enriched about 90-fold by sequential chromatography including affinity chromatography to a cerulenin-based inhibitor of palmitoylation. The partially purified PAT activity (1) was lost with treatments to degrade or denature proteins, (2) could acylate tubulin, Galpha(i) and RGS16 and (3) showed a preference for palmitate and to a lesser degree other long-chain fatty acids. This purification procedure is a significant advance over previous efforts at PAT purification and a starting point for a proteomic approach for identification of mammalian PAT.
Asunto(s)
Aciltransferasas/aislamiento & purificación , Aciltransferasas/metabolismo , Hígado/enzimología , Acilación , Animales , Membrana Celular/enzimología , Cromatografía en Gel/métodos , Electroforesis en Gel de Poliacrilamida/métodos , Cinética , Masculino , Peso Molecular , Procesamiento Proteico-Postraduccional , Ratas , Especificidad por SustratoRESUMEN
Palmitoylation is a reversible post-translational modification used by cells to regulate protein activity. The regulator of G-protein signaling (RGS) proteins RGS4 and RGS16 share conserved cysteine (Cys) residues that undergo palmitoylation. In the accompanying article (Hiol, A., Davey, P. C., Osterhout, J. L., Waheed, A. A., Fischer, E. R., Chen, C. K., Milligan, G., Druey, K. M., and Jones, T. L. Z. (2003) J. Biol. Chem. 278, 19301-19308), we determined that mutation of NH2-terminal cysteine residues in RGS16 (Cys-2 and Cys-12) reduced GTPase accelerating (GAP) activity toward a 5-hydroxytryptamine (5-HT1A)/G alpha o1 receptor fusion protein in cell membranes. NH2-terminal acylation also permitted palmitoylation of a cysteine residue in the RGS box of RGS16 (Cys-98). Here we investigated the role of internal palmitoylation in RGS16 localization and GAP activity. Mutation of RGS16 Cys-98 or RGS4 Cys-95 to alanine reduced GAP activity on the 5-HT1A/G alpha o1 fusion protein and regulation of adenylyl cyclase inhibition. The C98A mutation had no effect on RGS16 localization or GAP activity toward purified G-protein alpha subunits. Enzymatic palmitoylation of RGS16 resulted in internal palmitoylation on residue Cys-98. Palmitoylated RGS16 or RGS4 WT but not C98A or C95A preincubated with membranes expressing 5-HT1a/G alpha o1 displayed increased GAP activity over time. These results suggest that palmitoylation of a Cys residue in the RGS box is critical for RGS16 and RGS4 GAP activity and their ability to regulate Gi-coupled signaling in mammalian cells.
Asunto(s)
Cisteína/metabolismo , GTP Fosfohidrolasas/metabolismo , Subunidades alfa de la Proteína de Unión al GTP Gi-Go/fisiología , Ácido Palmítico/metabolismo , Proteínas/fisiología , Proteínas RGS/fisiología , Transducción de Señal , Inhibidores de Adenilato Ciclasa , Animales , Sitios de Unión , Células COS , Caveolina 1 , Caveolinas/análisis , Línea Celular , Membrana Celular/química , Membrana Celular/enzimología , Escherichia coli/química , Subunidades alfa de la Proteína de Unión al GTP Gi-Go/análisis , Proteínas Activadoras de GTPasa/fisiología , Humanos , Lípidos de la Membrana/análisis , Ratones , Modelos Moleculares , Mutagénesis , Toxina del Pertussis/farmacología , Proteínas/análisis , Proteínas/genética , Proteínas RGS/análisis , Proteínas RGS/química , Proteínas RGS/genética , Ratas , Proteínas Recombinantes de Fusión/aislamiento & purificación , Proteínas Recombinantes de Fusión/metabolismo , Somatostatina/farmacología , Relación Estructura-Actividad , TransfecciónRESUMEN
Regulators of G-protein signaling (RGS) proteins down-regulate signaling by heterotrimeric G-proteins by accelerating GTP hydrolysis on the G alpha subunits. Palmitoylation, the reversible addition of palmitate to cysteine residues, occurs on several RGS proteins and is critical for their activity. For RGS16, mutation of Cys-2 and Cys-12 blocks its incorporation of [3H]palmitate and ability to turn-off Gi and Gq signaling and significantly inhibited its GTPase activating protein activity toward aG alpha subunit fused to the 5-hydroxytryptamine receptor 1A, but did not reduce its plasma membrane localization based on cell fractionation studies and immunoelectron microscopy. Palmitoylation can target proteins, including many signaling proteins, to membrane microdomains, called lipid rafts. A subpopulation of endogenous RGS16 in rat liver membranes and overexpressed RGS16 in COS cells, but not the nonpalmitoylated cysteine mutant of RGS16, localized to lipid rafts. However, disruption of lipid rafts by treatment with methyl-beta-cyclodextrin did not decrease the GTPase activating protein activity of RGS16. The lipid raft fractions were enriched in protein acyltransferase activity, and RGS16 incorporated [3H]palmitate into a peptide fragment containing Cys-98, a highly conserved cysteine within the RGS box. These results suggest that the amino-terminal palmitoylation of an RGS protein promotes its lipid raft targeting that allows palmitoylation of a poorly accessible cysteine residue that we show in the accompanying article (Osterhout, J. L., Waheed, A. A., Hiol, A., Ward, R. J., Davey, P. C., Nini, L., Wang, J., Milligan, G., Jones, T. L. Z., and Druey, K. M. (2003) J. Biol. Chem. 278, 19309-19316) was critical for RGS16 and RGS4 GAP activity.