메뉴 건너뛰기




Volumn 129, Issue 2, 2004, Pages 111-131

The 2003 ASBMB-Avanti Award in Lipids Address: Applications of novel synthetic lipids to biological problems

Author keywords

Alphavirus; Antitumor lipid; Ceramide; Cytolysin; Glycosphingolipids; Lysophosphospholipids

Indexed keywords

AMINO ACID DERIVATIVE; ANTINEOPLASTIC AGENT; CERAMIDE DERIVATIVE; CEREBROSIDE; CHOLESTEROL; CHOLINE DERIVATIVE; CYTOLYSIN; GLYCOSPHINGOLIPID; LIPID; LYSOPHOSPHATIDIC ACID; N OCTANOYLCERAMIDE; PROTEIN DERIVATIVE; SPHINGOMYELIN; SPHINGOSINE 1 PHOSPHATE; UNCLASSIFIED DRUG;

EID: 1842814985     PISSN: 00093084     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.chemphyslip.2004.01.004     Document Type: Review
Times cited : (30)

References (67)
  • 1
    • 0036118329 scopus 로고    scopus 로고
    • The fusion peptide of Semliki Forest virus associates with sterol-rich membrane domains
    • Ahn A., Gibbons D.L., Kielian M. The fusion peptide of Semliki Forest virus associates with sterol-rich membrane domains. J. Virol. 76:2002;3267-3275.
    • (2002) J. Virol. , vol.76 , pp. 3267-3275
    • Ahn, A.1    Gibbons, D.L.2    Kielian, M.3
  • 2
    • 0032484959 scopus 로고    scopus 로고
    • The inhibition of cell signaling pathways by antitumor ether lipids
    • Arthur G., Bittman R. The inhibition of cell signaling pathways by antitumor ether lipids. Biochim. Biophys. Acta. 1390:1998;85-102.
    • (1998) Biochim. Biophys. Acta , vol.1390 , pp. 85-102
    • Arthur, G.1    Bittman, R.2
  • 4
    • 0027527545 scopus 로고
    • Selectivity of ceramide-mediated biology. Lack of activity of erythro-dihydroceramide
    • Bielawska A., Crane H.M., Liotta D., Obeid L.M., Hannun Y.A. Selectivity of ceramide-mediated biology. Lack of activity of erythro-dihydroceramide. J. Biol. Chem. 268:1993;26226-26232.
    • (1993) J. Biol. Chem. , vol.268 , pp. 26226-26232
    • Bielawska, A.1    Crane, H.M.2    Liotta, D.3    Obeid, L.M.4    Hannun, Y.A.5
  • 5
    • 0028208246 scopus 로고
    • Isosteric phosphonate analogs of ET-16-OMe. Synthesis and biological evaluation of the enantiomers of 2′-(trimethylammonio)ethyl 4-(hexadecyloxy)-3-methoxybutanephosphonate and 2′-(trimethylammonio)ethyl 4-(hexadecylthio)-3-methoxybutanephosphonate
    • Bittman R., Byun H.-S., Mercier B., Salari H. Isosteric phosphonate analogs of ET-16-OMe. Synthesis and biological evaluation of the enantiomers of 2′-(trimethylammonio)ethyl 4-(hexadecyloxy)-3-methoxybutanephosphonate and 2′-(trimethylammonio)ethyl 4-(hexadecylthio)-3-methoxybutanephosphonate. J. Med. Chem. 37:1994;425-430.
    • (1994) J. Med. Chem. , vol.37 , pp. 425-430
    • Bittman, R.1    Byun, H.-S.2    Mercier, B.3    Salari, H.4
  • 6
    • 0029936609 scopus 로고    scopus 로고
    • Inhibitors of lipid phosphatidate receptors: N-palmitoyl-serine and N-palmitoyl-tyrosine phosphoric acids
    • Bittman R., Swords B., Liliom K., Tigyi G. Inhibitors of lipid phosphatidate receptors: N-palmitoyl-serine and N-palmitoyl-tyrosine phosphoric acids. J. Lipid Res. 37:1996;391-398.
    • (1996) J. Lipid Res. , vol.37 , pp. 391-398
    • Bittman, R.1    Swords, B.2    Liliom, K.3    Tigyi, G.4
  • 7
    • 0024370455 scopus 로고
    • Photochemical labeling of apolar phase of membranes
    • Brunner J. Photochemical labeling of apolar phase of membranes. Methods Enzymol. 172:1989;628-687.
    • (1989) Methods Enzymol. , vol.172 , pp. 628-687
    • Brunner, J.1
  • 8
    • 0036083829 scopus 로고    scopus 로고
    • Rab proteins mediate Golgi transport of caveola-internalized glycosphingolipids and correct lipid trafficking in Niemann-Pick C cells
    • Choudhury A., Dominguez M., Puri V., Sharma D.K., Narita K., Wheatley C.L., Marks D.L., Pagano R.E. Rab proteins mediate Golgi transport of caveola-internalized glycosphingolipids and correct lipid trafficking in Niemann-Pick C cells. J. Clin. Invest. 109:2002;1541-1550.
    • (2002) J. Clin. Invest. , vol.109 , pp. 1541-1550
    • Choudhury, A.1    Dominguez, M.2    Puri, V.3    Sharma, D.K.4    Narita, K.5    Wheatley, C.L.6    Marks, D.L.7    Pagano, R.E.8
  • 9
    • 0034602274 scopus 로고    scopus 로고
    • Synthesis of ceramide analogues having the C(4)-C(5) bond of the long-chain base as part of an aromatic or heteroaromatic system
    • Chun J., He L., Byun H.-S., Bittman R. Synthesis of ceramide analogues having the C(4)-C(5) bond of the long-chain base as part of an aromatic or heteroaromatic system. J. Org. Chem. 65:2000;7634-7640.
    • (2000) J. Org. Chem. , vol.65 , pp. 7634-7640
    • Chun, J.1    He, L.2    Byun, H.-S.3    Bittman, R.4
  • 11
    • 0037462398 scopus 로고    scopus 로고
    • Synthesis and growth inhibitory activity of chiral 5-hydroxy-2-N-acyl- (3E)-sphingenines: Ceramides with an unusual sphingoid backbone
    • Chun J., Byun H.-S., Arthur G., Bittman R. Synthesis and growth inhibitory activity of chiral 5-hydroxy-2-N-acyl-(3E)-sphingenines: ceramides with an unusual sphingoid backbone. J. Org. Chem. 68:2003a;355-359.
    • (2003) J. Org. Chem. , vol.68 , pp. 355-359
    • Chun, J.1    Byun, H.-S.2    Arthur, G.3    Bittman, R.4
  • 12
    • 0037462337 scopus 로고    scopus 로고
    • First asymmetric synthesis of 6-hydroxy-4-sphingenine-containing ceramides. Use of chiral propargylic alcohols to prepare a lipid found in human skin
    • Chun J., Byun H.-S., Bittman R. First asymmetric synthesis of 6-hydroxy-4-sphingenine-containing ceramides. Use of chiral propargylic alcohols to prepare a lipid found in human skin. J. Org. Chem. 68:2003b;348-354.
    • (2003) J. Org. Chem. , vol.68 , pp. 348-354
    • Chun, J.1    Byun, H.-S.2    Bittman, R.3
  • 13
    • 0028235205 scopus 로고
    • Benzophenone photoprobes in biochemistry
    • Dormán G., Prestwich G.D. Benzophenone photoprobes in biochemistry. Biochemistry. 33:1994;5661-5673.
    • (1994) Biochemistry , vol.33 , pp. 5661-5673
    • Dormán, G.1    Prestwich, G.D.2
  • 14
    • 0038637713 scopus 로고    scopus 로고
    • Cholesterol in bilayers of sphingomyelin or dihydrosphingomyelin at concentrations found in ocular lens membranes
    • Epand R.M. Cholesterol in bilayers of sphingomyelin or dihydrosphingomyelin at concentrations found in ocular lens membranes. Biophys. J. 84:2003;3102-3110.
    • (2003) Biophys. J. , vol.84 , pp. 3102-3110
    • Epand, R.M.1
  • 15
    • 12244310530 scopus 로고    scopus 로고
    • Activation of human monocytic cells by lysophosphatidic acid and sphingosine-1-phosphate
    • Füller, M., Wang, de A., Tigyi, G., Siess, W., 2003. Activation of human monocytic cells by lysophosphatidic acid and sphingosine-1-phosphate. Cell Signal. 15, 367-375.
    • (2003) Cell Signal , vol.15 , pp. 367-375
    • Füller, M.1    De Wang, A.2    Tigyi, G.3    Siess, W.4
  • 17
    • 0036783411 scopus 로고    scopus 로고
    • 3 (edelfosine), a proapoptotic agent in tumor cells
    • 3 (edelfosine), a proapoptotic agent in tumor cells. Curr. Drug Metab. 3:2002;491-525.
    • (2002) Curr. Drug Metab. , vol.3 , pp. 491-525
    • Gajate, C.1    Mollinedo, F.2
  • 19
    • 0034602328 scopus 로고    scopus 로고
    • Stereoselective preparation of ceramide and its skeleton backbone modified analogues via cyclic thionocarbonate intermediates derived by catalytic asymmetric dihydroxylation of α,β-unsaturated ester precursors
    • He L., Byun H.-S., Bittman R. Stereoselective preparation of ceramide and its skeleton backbone modified analogues via cyclic thionocarbonate intermediates derived by catalytic asymmetric dihydroxylation of α,β-unsaturated ester precursors. J. Org. Chem. 65:2000;7627-7633.
    • (2000) J. Org. Chem. , vol.65 , pp. 7627-7633
    • He, L.1    Byun, H.-S.2    Bittman, R.3
  • 20
    • 0035206909 scopus 로고    scopus 로고
    • Activity of 2-substituted lysophosphatidic acid (LPA) analogs at LPA receptors: Discovery of a LPA1/LPA3 receptor antagonist
    • Heise C.E., Santos W.L., Schreihofer A.M., Heasley B.H., Mukhin Y.V., Macdonald T.L., Lynch K.R. Activity of 2-substituted lysophosphatidic acid (LPA) analogs at LPA receptors: discovery of a LPA1/LPA3 receptor antagonist. Mol. Pharmacol. 60:2001;1173-1180.
    • (2001) Mol. Pharmacol. , vol.60 , pp. 1173-1180
    • Heise, C.E.1    Santos, W.L.2    Schreihofer, A.M.3    Heasley, B.H.4    Mukhin, Y.V.5    MacDonald, T.L.6    Lynch, K.R.7
  • 21
    • 0037401876 scopus 로고    scopus 로고
    • Signaling and biological actions of sphingosine 1-phosphate
    • Hla T. Signaling and biological actions of sphingosine 1-phosphate. Pharmacol. Res. 47:2003;401-407.
    • (2003) Pharmacol. Res. , vol.47 , pp. 401-407
    • Hla, T.1
  • 22
    • 0033065591 scopus 로고    scopus 로고
    • A microscopic interaction model of maximum solubility of cholesterol in lipid bilayers
    • Huang J., Feigenson G.W. A microscopic interaction model of maximum solubility of cholesterol in lipid bilayers. Biophys. J. 76:1999;2142-2157.
    • (1999) Biophys. J. , vol.76 , pp. 2142-2157
    • Huang, J.1    Feigenson, G.W.2
  • 23
    • 0031756497 scopus 로고    scopus 로고
    • The role of ceramide in the cellular response to cytotoxic agents
    • Jarvis W.D., Grant S. The role of ceramide in the cellular response to cytotoxic agents. Curr. Opin. Oncol. 10:1998;552-559.
    • (1998) Curr. Opin. Oncol. , vol.10 , pp. 552-559
    • Jarvis, W.D.1    Grant, S.2
  • 24
    • 0030000464 scopus 로고    scopus 로고
    • Stereospecific induction of apoptosis in U937 cells by N-octanoylsphingosine stereoisomers and N-octylsphingosine. The ceramide amide group is not required for apoptosis
    • Karasavvas N., Erukulla R.K., Bittman R., Lockshin R., Zakeri Z. Stereospecific induction of apoptosis in U937 cells by N-octanoylsphingosine stereoisomers and N-octylsphingosine. The ceramide amide group is not required for apoptosis. Eur. J. Biochem. 236:1996;729-737.
    • (1996) Eur. J. Biochem. , vol.236 , pp. 729-737
    • Karasavvas, N.1    Erukulla, R.K.2    Bittman, R.3    Lockshin, R.4    Zakeri, Z.5
  • 25
    • 0029840915 scopus 로고    scopus 로고
    • Mechanisms of mutations inhibiting fusion and infection by Semliki Forest virus
    • Kielian M., Klimjack M.R., Ghosh S., Duffus W.A. Mechanisms of mutations inhibiting fusion and infection by Semliki Forest virus. J. Cell Biol. 134:1996;863-872.
    • (1996) J. Cell Biol. , vol.134 , pp. 863-872
    • Kielian, M.1    Klimjack, M.R.2    Ghosh, S.3    Duffus, W.A.4
  • 26
    • 0031919157 scopus 로고    scopus 로고
    • Regulation of ceramide production and apoptosis
    • Kolesnick R.N., Kronke M. Regulation of ceramide production and apoptosis. Annu. Rev. Physiol. 60:1998;643-665.
    • (1998) Annu. Rev. Physiol. , vol.60 , pp. 643-665
    • Kolesnick, R.N.1    Kronke, M.2
  • 28
    • 0029832759 scopus 로고    scopus 로고
    • N-Palmitoyl-serine and N-palmitoyl-tyrosine phosphoric acids are selective competitive antagonists of the lysophosphatidic acid receptors
    • Liliom K., Bittman R., Swords B., Tigyi G. N-Palmitoyl-serine and N-palmitoyl-tyrosine phosphoric acids are selective competitive antagonists of the lysophosphatidic acid receptors. Mol. Pharmacol. 50:1996;616-623.
    • (1996) Mol. Pharmacol. , vol.50 , pp. 616-623
    • Liliom, K.1    Bittman, R.2    Swords, B.3    Tigyi, G.4
  • 29
    • 0028597086 scopus 로고
    • Antitumor ether lipids and alkylphosphocholines
    • Lohmeyer M., Bittman R. Antitumor ether lipids and alkylphosphocholines. Drugs Fut. 19:1994;1021-1037.
    • (1994) Drugs Fut. , vol.19 , pp. 1021-1037
    • Lohmeyer, M.1    Bittman, R.2
  • 30
    • 0026649321 scopus 로고
    • Lack of enantioselectivity in the in vitro antitumor cytotoxicity and membrane - Damaging activity of ether lipid SRI 62-834: Further evidence for a nonreceptor-mediated mechanism of action
    • Lohmeyer M., Workman P. Lack of enantioselectivity in the in vitro antitumor cytotoxicity and membrane - damaging activity of ether lipid SRI 62-834: further evidence for a nonreceptor-mediated mechanism of action. Biochem. Pharmacol. 44:1992;819-823.
    • (1992) Biochem. Pharmacol. , vol.44 , pp. 819-823
    • Lohmeyer, M.1    Workman, P.2
  • 31
    • 0042839476 scopus 로고    scopus 로고
    • Total synthesis of two photoactivatable analogues of the growth-factor-like mediator sphingosine 1-phosphate: Differential interaction with protein targets
    • Lu X., Cseh S., Byun H.-S., Tigyi G., Bittman R. Total synthesis of two photoactivatable analogues of the growth-factor-like mediator sphingosine 1-phosphate: differential interaction with protein targets. J. Org. Chem. 68:2003;7046-7050.
    • (2003) J. Org. Chem. , vol.68 , pp. 7046-7050
    • Lu, X.1    Cseh, S.2    Byun, H.-S.3    Tigyi, G.4    Bittman, R.5
  • 32
    • 0037205423 scopus 로고    scopus 로고
    • Sphingomyelin modulates the transbilayer distribution of galactosylceramide in phospholipid membranes
    • Mattjus P., Malewicz B., Valiyaveettil J.T., Baumann W.J., Bittman R., Brown R.E. Sphingomyelin modulates the transbilayer distribution of galactosylceramide in phospholipid membranes. J. Biol. Chem. 277:2002;19476-19481.
    • (2002) J. Biol. Chem. , vol.277 , pp. 19476-19481
    • Mattjus, P.1    Malewicz, B.2    Valiyaveettil, J.T.3    Baumann, W.J.4    Bittman, R.5    Brown, R.E.6
  • 35
    • 0029112141 scopus 로고
    • Sphingolipids activate membrane fusion of Semliki Forest virus in a stereospecific manner
    • Moesby L., Corver J., Erukulla R.K., Bittman R., Wilschut J. Sphingolipids activate membrane fusion of Semliki Forest virus in a stereospecific manner. Biochemistry. 34:1995;10319-10324.
    • (1995) Biochemistry , vol.34 , pp. 10319-10324
    • Moesby, L.1    Corver, J.2    Erukulla, R.K.3    Bittman, R.4    Wilschut, J.5
  • 37
    • 0035744047 scopus 로고    scopus 로고
    • Updates on functions of ceramide in chemotherapy-induced cell death and in multidrug resistance
    • Ogretman B., Hannun Y.A. Updates on functions of ceramide in chemotherapy-induced cell death and in multidrug resistance. Drug Resist. Update. 4:2001;368-377.
    • (2001) Drug Resist. Update , vol.4 , pp. 368-377
    • Ogretman, B.1    Hannun, Y.A.2
  • 38
    • 0034567169 scopus 로고    scopus 로고
    • Applications of BODIPY-sphingolipid analogs to study lipid traffic and metabolism in cells
    • Pagano R.E., Watanabe R., Wheatley C., Dominguez M. Applications of BODIPY-sphingolipid analogs to study lipid traffic and metabolism in cells. Methods Enzymol. 312:2000;523-534.
    • (2000) Methods Enzymol. , vol.312 , pp. 523-534
    • Pagano, R.E.1    Watanabe, R.2    Wheatley, C.3    Dominguez, M.4
  • 39
    • 0037203342 scopus 로고    scopus 로고
    • Ceramide in apoptosis: An overview and current perspectives
    • Pettus B.J., Chalfant C.E., Hannun Y.A. Ceramide in apoptosis: an overview and current perspectives. Biochim. Biophys. Acta. 1585:2002;114-125.
    • (2002) Biochim. Biophys. Acta , vol.1585 , pp. 114-125
    • Pettus, B.J.1    Chalfant, C.E.2    Hannun, Y.A.3
  • 41
    • 0037375586 scopus 로고    scopus 로고
    • Designing anticancer drugs via the Achilles heel: Ceramide, allylic ketones, and mitochondria
    • Radin N.S. Designing anticancer drugs via the Achilles heel: ceramide, allylic ketones, and mitochondria. Bioorg. Med. Chem. 11:2003;2123-2142.
    • (2003) Bioorg. Med. Chem. , vol.11 , pp. 2123-2142
    • Radin, N.S.1
  • 42
    • 1842767829 scopus 로고    scopus 로고
    • Sphinx of fat
    • Raloff J. Sphinx of fat. Sci. News. 151:1997;342-343.
    • (1997) Sci. News , vol.151 , pp. 342-343
    • Raloff, J.1
  • 43
    • 0043020630 scopus 로고    scopus 로고
    • Subtype-selective antagonists of lysophosphatidic acid receptors inhibit platelet activation triggered by the lipid core of atherosclerotic plaques
    • Rother E., Brandl R., Baker D.L., Goyal P., Gebhard H., Tigyi G., Siess W. Subtype-selective antagonists of lysophosphatidic acid receptors inhibit platelet activation triggered by the lipid core of atherosclerotic plaques. Circulation. 108:2003;741-747.
    • (2003) Circulation , vol.108 , pp. 741-747
    • Rother, E.1    Brandl, R.2    Baker, D.L.3    Goyal, P.4    Gebhard, H.5    Tigyi, G.6    Siess, W.7
  • 44
    • 0037331989 scopus 로고    scopus 로고
    • Anti-cancer alkyl-lysophospholipids inhibit the phosphatidylinositol 3-kinase-Akt/PKB survival pathway
    • Ruiter G.A., Zerp S.F., Bartelink H., van Blitterswijk W.J., Verheij M. Anti-cancer alkyl-lysophospholipids inhibit the phosphatidylinositol 3-kinase-Akt/PKB survival pathway. Anticancer Drugs. 14:2003;167-173.
    • (2003) Anticancer Drugs , vol.14 , pp. 167-173
    • Ruiter, G.A.1    Zerp, S.F.2    Bartelink, H.3    Van Blitterswijk, W.J.4    Verheij, M.5
  • 45
    • 0037401894 scopus 로고    scopus 로고
    • Intracellular signal transduction pathways activated by ceramide and its metabolites
    • Ruvolo P.P. Intracellular signal transduction pathways activated by ceramide and its metabolites. Pharmacol. Res. 47:2003;383-392.
    • (2003) Pharmacol. Res. , vol.47 , pp. 383-392
    • Ruvolo, P.P.1
  • 49
    • 0032874859 scopus 로고    scopus 로고
    • Low-pH-dependent fusion of Sindbis virus with receptor-free cholesterol- and sphingolipid-containing liposomes
    • Smit J.M., Bittman R., Wilschut J. Low-pH-dependent fusion of Sindbis virus with receptor-free cholesterol- and sphingolipid-containing liposomes. J. Virol. 73:1999;8476-8484.
    • (1999) J. Virol. , vol.73 , pp. 8476-8484
    • Smit, J.M.1    Bittman, R.2    Wilschut, J.3
  • 51
    • 0242380863 scopus 로고    scopus 로고
    • Liposomes as target membranes in the study of virus-receptor interaction and membrane fusion
    • Smit J., Waarts B.-L., Bittman R., Wilschut J. Liposomes as target membranes in the study of virus-receptor interaction and membrane fusion. Methods Enzymol. 372:2003;374-392.
    • (2003) Methods Enzymol. , vol.372 , pp. 374-392
    • Smit, J.1    Waarts, B.-L.2    Bittman, R.3    Wilschut, J.4
  • 52
    • 0038218405 scopus 로고    scopus 로고
    • Sphingosine-1-phosphate: An enigmatic signaling lipid
    • Spiegel S., Milstien S. Sphingosine-1-phosphate: an enigmatic signaling lipid. Nat. Rev. Mol. Cell. Biol. 4:2003a;397-407.
    • (2003) Nat. Rev. Mol. Cell. Biol. , vol.4 , pp. 397-407
    • Spiegel, S.1    Milstien, S.2
  • 53
    • 0346788900 scopus 로고    scopus 로고
    • Exogenous and intracellularly generated sphingosine 1-phosphate can regulate cellular processes by divergent pathways
    • Spiegel S., Milstien S. Exogenous and intracellularly generated sphingosine 1-phosphate can regulate cellular processes by divergent pathways. Biochem. Soc. Trans. 31:2003b;1216-1219.
    • (2003) Biochem. Soc. Trans. , vol.31 , pp. 1216-1219
    • Spiegel, S.1    Milstien, S.2
  • 55
    • 0028088152 scopus 로고
    • The alphaviruses: Gene expression, replication, and evolution
    • Strauss J.H., Strauss E.G. The alphaviruses: gene expression, replication, and evolution. Microbiol. Rev. 58:1994;491-562.
    • (1994) Microbiol. Rev. , vol.58 , pp. 491-562
    • Strauss, J.H.1    Strauss, E.G.2
  • 57
    • 0141996371 scopus 로고    scopus 로고
    • Molecular mechanisms of lysophosphatidic acid action
    • Tigyi G., Parrill A.L. Molecular mechanisms of lysophosphatidic acid action. Prog. Lipid Res. 42:2003;498-526.
    • (2003) Prog. Lipid Res. , vol.42 , pp. 498-526
    • Tigyi, G.1    Parrill, A.L.2
  • 58
    • 0036683314 scopus 로고    scopus 로고
    • Human platelets respond differentially to lysophosphatidic acids having a highly unsaturated fatty acyl group and alkyl ether-linked lysophosphatidic acids
    • Tokumura A., Sinomiya J., Kishimoto S., Tanaka T., Kogure K., Sugiura T., Satouchi K., Waku K., Fukuzawa K. Human platelets respond differentially to lysophosphatidic acids having a highly unsaturated fatty acyl group and alkyl ether-linked lysophosphatidic acids. Biochem. J. 365:2002;617-628.
    • (2002) Biochem. J. , vol.365 , pp. 617-628
    • Tokumura, A.1    Sinomiya, J.2    Kishimoto, S.3    Tanaka, T.4    Kogure, K.5    Sugiura, T.6    Satouchi, K.7    Waku, K.8    Fukuzawa, K.9
  • 59
    • 0346367067 scopus 로고    scopus 로고
    • Lipid raft microdomains: Key sites for Coxsackievirus A9 infectious cycle
    • Triantafilou K., Triantafilou M. Lipid raft microdomains: key sites for Coxsackievirus A9 infectious cycle. Virology. 317:2003;128-135.
    • (2003) Virology , vol.317 , pp. 128-135
    • Triantafilou, K.1    Triantafilou, M.2
  • 60
    • 0037063998 scopus 로고    scopus 로고
    • Sphingolipid and cholesterol dependence of alphavirus membrane fusion. Lack of correlation with lipid raft formation in target liposomes
    • Waarts B.-L., Bittman R., Wilschut J. Sphingolipid and cholesterol dependence of alphavirus membrane fusion. Lack of correlation with lipid raft formation in target liposomes. J. Biol. Chem. 277:2002;38141-38147.
    • (2002) J. Biol. Chem. , vol.277 , pp. 38141-38147
    • Waarts, B.-L.1    Bittman, R.2    Wilschut, J.3
  • 61
    • 0029201982 scopus 로고
    • Fusion of Semliki Forest virus with cholesterol-containing liposomes at low pH: A specific requirement for sphingolipids
    • Wilschut J., Corver J., Nieva J.L., Bron R., Moesby L., Reddy K.C., Bittman R. Fusion of Semliki Forest virus with cholesterol-containing liposomes at low pH: a specific requirement for sphingolipids. Mol. Membr. Biol. 12:1995;143-149.
    • (1995) Mol. Membr. Biol. , vol.12 , pp. 143-149
    • Wilschut, J.1    Corver, J.2    Nieva, J.L.3    Bron, R.4    Moesby, L.5    Reddy, K.C.6    Bittman, R.7
  • 65
    • 0030793119 scopus 로고    scopus 로고
    • Mode of primary binding to target membranes and pore formation induced by Vibrio cholerae cytolysin (hemolysin)
    • Zitzer A., Palmer M., Weller U., Wassenaar T., Biermann C., Tranum-Jensen J., Bhakdi S. Mode of primary binding to target membranes and pore formation induced by Vibrio cholerae cytolysin (hemolysin). Eur. J. Biochem. 247:1997;209-216.
    • (1997) Eur. J. Biochem. , vol.247 , pp. 209-216
    • Zitzer, A.1    Palmer, M.2    Weller, U.3    Wassenaar, T.4    Biermann, C.5    Tranum-Jensen, J.6    Bhakdi, S.7
  • 66
    • 0033556418 scopus 로고    scopus 로고
    • Oligomerization of Vibrio cholerae cytolysin yields a pentameric pore and has a dual specificity for cholesterol and sphingolipids in the target membrane
    • Zitzer A., Zitzer O., Bhakdi S., Palmer M. Oligomerization of Vibrio cholerae cytolysin yields a pentameric pore and has a dual specificity for cholesterol and sphingolipids in the target membrane. J. Biol. Chem. 274:1999;1375-1380.
    • (1999) J. Biol. Chem. , vol.274 , pp. 1375-1380
    • Zitzer, A.1    Zitzer, O.2    Bhakdi, S.3    Palmer, M.4
  • 67
    • 0035805608 scopus 로고    scopus 로고
    • Coupling of cholesterol and cone-shaped lipids in bilayers augments membrane permeabilization by the cholesterol-specific toxins streptolysin O and Vibrio cholerae cytolysin
    • Zitzer A., Bittman R., Verbicky C.A., Erukulla R.K., Bhakdi S., Weis S., Valeva A., Palmer M. Coupling of cholesterol and cone-shaped lipids in bilayers augments membrane permeabilization by the cholesterol-specific toxins streptolysin O and Vibrio cholerae cytolysin. J. Biol. Chem. 276:2001;14628-14633.
    • (2001) J. Biol. Chem. , vol.276 , pp. 14628-14633
    • Zitzer, A.1    Bittman, R.2    Verbicky, C.A.3    Erukulla, R.K.4    Bhakdi, S.5    Weis, S.6    Valeva, A.7    Palmer, M.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.