The topological analysis of integral cytoplasmic membrane proteins
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Summary
We review three general approaches to determining the topology of integral cytoplasmic membrane proteins. (i) Inspection of the amino acid sequence and use of algorithms to predict membrane spanning segments allows the construction of topological models. For many proteins, the mere identification of such segments and an analysis of the distribution of basic amino acids in hydrophilic domains leads to correct structure predictions. For others, additional factors must come into play in determining topology, (ii) Gene fusion analysis of membrane proteins, in many cases, leads to complete topological models. Such analyses have been carried out in both bacteria and in the yeast Saccharomyces cerevisiae. Conflicts between results from gene fusion analysis and other approaches can be used to explore details of the process of membrane protein assembly. For instance, anomalies in gene fusion studies contributed evidence for the important role of basic amino acids in determining topolog. (iii) Biochemical probes and the site of natural biochemical modifications of membrane proteins give information on their topology. Chemical modifiers, proteases and antibodies made to different domains of a membrane protein can identify which segments of the protein are in the cytoplasm and which are on the extracytoplasmic side of the membrane. Sites of such modifications as glycosylation and phosphorylation help to specify the location of particular hydrophilic domains. The advantages and limitations of these methods are discussed.
Key Words
gene fusion topology membrane protein membrane spanning segment protein structurePreview
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References
- 1.Ahmad, M., Bussey, H. 1988. Mol. Microbiol., 2:627–635Google Scholar
- 2.Altenbach, C., Marti, T., Khorana, H.G., Hubbell, W.L. 1990. Science 248:1088–1092Google Scholar
- 3.Andersson, H., Bakker, E., von Heijne, G. 1992. J. Biol. Chem. 267:1491–1495Google Scholar
- 4.Ballesteros, J.A., Weinstein, H. 1992. Biophys. J. 62:127–128Google Scholar
- 5.Beckwith, J., Silhavy, T.J. 1992. The Power of Bacterial Genetics: A Literature-Based Course. Cold Spring Harbor Laboratory PlainviewGoogle Scholar
- 6.Blobel, G. 1980. Proc. Natl. Acad. Sci. USA 77:1496–1500Google Scholar
- 7.Bowler, L.D., Spratt, B.G. 1989. Mol. Microbiol., 3:1277–1286Google Scholar
- 8.Boyd, D., Beckwith, J. 1989. Proc. Natl. Acad. Sci. USA 86:9446–9450Google Scholar
- 9.Boyd, D., Beckwith, J. 1990. Cell 62:1031–1033Google Scholar
- 10.Boyd, D., Manoil, C., Beckwith, J. 1987. Proc. Natl. Acad. Sci. USA 84:8525–8529Google Scholar
- 11.Broome-Smith, J.K., Tadayyon, M., Zhang, Y. 1990. Mol. Microbiol., 4:1637–1644Google Scholar
- 12.Calamia, J., Manoil, C. 1990. Proc. Natl. Acad. Sci. USA 87:4937–4941Google Scholar
- 13.Calamia, J., Manoil, C. 1992. J. Mol. Biol. 224:539–543Google Scholar
- 14.Carrasco, N., Herzlinger, D., Danho, W., Kaback, H.R 1986. Meth. Enzymol. 125:453–467Google Scholar
- 15.Chavez, R.A., Hall, Z.W. 1991. J. Biol. Chem. 266: 15532–15538Google Scholar
- 16.Chun, S., Parkinson, J.S. 1988. Science 239:276–278Google Scholar
- 17.Crimi, M., Degli Esposti, M. 1991. TIBS 16:119–119Google Scholar
- 18.Cronan, J.E., Jr. 1990. J. Biol. Chem. 265:10327–10333Google Scholar
- 19.Dalbey, R.E. 1990. TIBS 15:253–257Google Scholar
- 20.Davies, A., Ciardelli, T.L., Lienhard, G.E., Boyle, J.M., Whetton, A.D., Baldwin, S.A. 1990. Biochem. J. 266:799–808Google Scholar
- 21.Derman, A.I., Beckwith, J. 1991. J. Bacteriol. 173s:7719–7722Google Scholar
- 22.Deshaies, R.J., Schekman, R. 1990. Mol. Cell. Biol., 10:6024–6035Google Scholar
- 23.Dohlman, H.G., Bouvier, M., Benovic, J.L., Caron, M.G., Lefkowitz, R.J. 1987. J. Biol. Chem. 262:14282–14288Google Scholar
- 24.Duchêne, A.M., Patte, J., Gutierrez, C., Chandler, M. 1992. Gene 114:103–107Google Scholar
- 25.Edelman, A.M., Blumenthal, D.K., Krebs, E.G. 1987. Annu. Rev. Biochem. 56:567–613Google Scholar
- 26.Ehrmann, M., Boyd, D., Beckwith, J. 1990. Proc. Natl. Acad. Sci. USA 87:7574–7578Google Scholar
- 27.Eisenberg, D. 1984. Annu. Rev. Biochem. 53:595–623Google Scholar
- 28.Fasman, G.D., Gilbert, W.A. 1990. TIBS 15:89–92Google Scholar
- 29.Freissmuth, M., Selzer, E., Marullo, S., Schültz, W., Strosberg, A.D. 1991. Proc. Natl. Acad. Sci. USA 88:8548–8552Google Scholar
- 30.Froshauer, S., Green, G.N., Boyd, D., McGovern, K., Beckwith, J. 1988. J. Mol. Biol. 200:501–511Google Scholar
- 31.Gardel, C., Johnson, K., Jacq, A., Beckwith, J. 1990. EMBO J. 9:3209–3216Google Scholar
- 32.Georgiou, C.D., Dueweke, T.J., Gennis, R.B. 1988. J. Biol. Chem. 263:13130–13137Google Scholar
- 33.Green, G.N., Hansen, W., Walter, P. 1989. J. Cell Sci. Suppl. 11:109–113Google Scholar
- 34.Hertzberg, E.L., Hinkle, P.C. 1974. Biochem. Biophys. Res. Comm. 58:178–184Google Scholar
- 35.Hoffman, C., Wright, A. 1985. Proc. Natl. Acad. Sci. USA 82:5107–5111Google Scholar
- 36.Huang, K.-S., Bayley, H., Liao, M.-J., London, E., Khorana, H.G. 1981. J. Biol. Chem. 256:3802–3809Google Scholar
- 37.Hunter, T., Cooper, J.A. 1985. Annu. Rev. Biochem. 54:897–930Google Scholar
- 38.Jennings, M.L. 1989. Annu. Rev. Biochem. 58:999–1027Google Scholar
- 39.Kaback, H.R. 1971. Meth. Enzymol. 22:99–120Google Scholar
- 40.Klein, P., Kanehisa, M., DeLisi, C. 1985. Biochim. Biophys. Acta 815:468–476Google Scholar
- 41.Kornfeld, R., Kornfeld, S. 1985. Annu. Rev. Biochem. 54:631–664Google Scholar
- 42.Kyte, J., Doolittle, R.F., 1982. J. Mol. Biol. 157:105–132Google Scholar
- 43.Laws, J.K., Dalbey, R.E. 1989. EMBO J. 8:2095–2099Google Scholar
- 44.Lee, C., Li, P., Inouye, H., Beckwith, J. 1989. J. Bacteriol. 171:4609–4616Google Scholar
- 45.Maher, P.A., Singer, S.J. 1986. Proc. Natl. Acad. Sci. USA 83:9001–9005Google Scholar
- 46.Maloney-Huss, K., Lybrand, T. 1992. J. Mol. Biol. 225:859–871Google Scholar
- 47.Manoil, C. 1990. J. Bacteriol. 172:1035–1042Google Scholar
- 48.Manoil, C., Beckwith, J. 1985. Proc. Natl. Acad. Sci. USA 82:8129–8133Google Scholar
- 49.Manoil, C., Beckwith, J. 1986. Science 233:1403–1408Google Scholar
- 50.McCrea, P.D., Engleman, D.M., Popot, J.-L. 1988. TIBS 13:289–290Google Scholar
- 51.McGovern, K., Ehrmann, M., Beckwith, J. 1991. EMBO J. 10:2773–2782Google Scholar
- 52.Michaelis, S., Inouye, I., Oliver, D., Beckwith, J. 1983. J. Bacteriol. 154:366–374Google Scholar
- 53.Mueckler, M., Caruso, C., Baldwin, S.A., Panico, M., Blench, I., Morris, H.R., Allard, W.J., Lienhard, G.E., Lodish, H.F. 1985. Science 230:941–945Google Scholar
- 54.Nilsson, I., von Heijne, G. 1990. Cell 62:1135–1141Google Scholar
- 55.Ovchinnikov, Y.A., Abdulaev, N.G., Vasilov, R.G., Vturina, I.Y., Kuryatov, A.B., Kiselev, A.V. 1985. FEBS Lett. 179:343–350Google Scholar
- 56.Page, M.G.P., Rosenbusch, J.P. 1988. J. Biol. Chem. 263:15906–15914Google Scholar
- 57.Popot, J.-L., Engelman, D.M. 1990. Biochemistry 29:4031–4037Google Scholar
- 58.Popot, J.-L., Gerchman, S.-E., Engelman, D.M. 1987. J. Mol. Biol. 198:655–676Google Scholar
- 59.Randall, L.L., Hardy, S.J.S. 1986. Cell 46:921–928Google Scholar
- 60.Rao, A., Martin, P., Reithmeier, R.A.F., Cantley, L.C. 1979. Biochemistry 18:4505–4516Google Scholar
- 61.Rao, J.K.M., Argos, P. 1986. Biochim. Biophys. Acta 869:197–214Google Scholar
- 62.Reed, K.E., Cronan, J.E., Jr. 1991. J. Biol. Chem. 266:11425–11428Google Scholar
- 63.San Millan, J.L., Boyd, D., Dalbey, R., Wickner, W., Beckwith, J. 1989. J. Bacteriol. 171:5536–5541Google Scholar
- 64.Sarkar, H.K., Thorens, B., Lodish, H.F., Kaback, H.R. 1988. Proc. Natl. Acad. Sci USA 85:5463–5467Google Scholar
- 65.Senstag, C., Stirling, C., Schekman, R., Rine, J. 1990. Mol. Cell Biol. 10:672–680Google Scholar
- 66.Singer, S.J. 1990. Annu. Rev. Cell Biol. 6:247–296Google Scholar
- 67.Steck, T.L. 1974. J. Cell Biol. 62:1–5Google Scholar
- 68.Stock, J.B., Ninfa, A.J., Stock, A.M. 1989. Microbiol. Rev. 53:450–490Google Scholar
- 69.Sugiyama, J.E., Mahmoodian, S., Jacobson, G.R. 1991. Proc. Natl. Acad. Sci. USA 88:9603–9607Google Scholar
- 70.Tadayyon, M., Broome-Smith, J.K. 1992. Gene 111:21–26Google Scholar
- 71.Traxler, B., Beckwith, J. 1992. Proc. Natl. Acad. Sci. USA 89:10852–10856.Google Scholar
- 72.Verrall, S., Hall, Z.W. 1992. Cell 68:23–31Google Scholar
- 73.von Heijne, G. 1986. EMBO J. 5:3021–3027Google Scholar
- 74.von Heijne, G. 1989. Nature 341:456–458Google Scholar
- 75.von Heijne, G., Gavel, Y. 1988. Eur. J. Biochem. 174:671–678Google Scholar
- 76.von Heijne, G., Manoil, C. 1990. Protein Engineering 4:109–112Google Scholar
- 77.Wang, H.-Y., Lipfert, L., Malbon, C.C., Bahouth, S. 1989. J. Biol. Chem. 264:14424–14431Google Scholar
- 78.Wilmes-Riesenberg, M.R., Wanner, B.L. 1992. J. Bacteriol. 174:4558–4575Google Scholar
- 79.Yaeger, M., Gilula, N.B. 1992. J. Mol. Biol. 223:929–948Google Scholar
- 80.Yu, X.-M., Hall, Z.W. 1991. Nature 352:64–67Google Scholar
- 81.Yun, C.-H., Van Doren, S.R., Crofts, A.R., Gennis, R.B. 1991. J. Biol.Chem. 266:10967–10973Google Scholar
- 82.Zhang, Y., Broome-Smith, J.K. 1990. Gene 96:51–57Google Scholar