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2001 | 48 | 2 |

Tytuł artykułu

Purification and functional reconstitution of intact ral-binding GTPase activating protein, RLIP76, in artificial liposomes

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
We have recently shown that RLIP76, a ral-bind ing GTPase ac ti vat ing pro tein, me­diates ATP-dependent transport of glutathione-conjugates (GS-E) and doxorubicin (DOX) (S. Awasthi eta/., Biochemistry39l9327l2000).TransportfunctionofRLIP76 was found to be in tact de spite con sid er able proteolytic frag men ta tion in prep a ra tions used for those stud ies, sug gest ing ei ther that the re sid ual in tact RLIP76 was re spon si ble for trans port ac tiv ity, or that the trans port ac tiv ity could be re con sti tuted by frag­ments of RLIP76. If the for mer were true, in tact RLIP76 would have a much higher spe cific ac tiv ity for ATP-hydrolysis than the frag mented pro tein. We have ad dressed this ques tion by com par ing trans port prop er ties of re com bi nant RLIP76 and hu man eryth ro cyte mem brane RLIP76 pu ri fied in buff ers treated with either 100 or 500uM serine pro te ase in hib i tor, PMSF. The pu rity and iden tity of re com bi nant and hu man eryth ro cyte RLIP76 was es tab lished by SDS/PAGE and West ern-blot anal y sis. These studies con firmed the or i gin of the 38 kDa pro tein, pre vi ously re ferred to as DNP-SG ATPase, from RLIP76. Higher PMSF con cen tra tion re sulted in lower yield of the 38 kDa band and higher yield of in tact RLIP76 from both hu man and re com bi nant source. In con trast, the sub strate-stimulated ATPase ac tiv ity in pres ence of DNP-SG, doxorubicin, daunorubicin, or colchicine were un af fected by in creased PMSF; similarly, ATP-dependent trans port of doxorubicin in proteo liposomes re con sti tuted with RLIP76 was un af fected by higher PMSF. These re sults in di cated that lim ited proteolysis by serine pro teas es does not ab ro gate the trans port func tion of RLIP76. Com parison of trans port ki net ics for daunorubicin be tween re com bi nant vs hu man erythrocyte RLIP76 re vealed higher spe cific ac tiv ity of trans port for tis sue pu ri fied RLIP76, in di cat ing that ad di tional fac tors pres ent in tis sue pu ri fied RLIP76 can mod u late its transport activity.

Wydawca

-

Rocznik

Tom

48

Numer

2

Opis fizyczny

p.551-562,fig.

Twórcy

  • The University of Texas at Arlington, Arlington, TX, USA
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Bibliografia

  • 1.Awasthi, S., Cheng, J., Singhal, S.S., Pandya, U., Pikula, S., Pikula, J., Singh, S.V, Zimniak, P. & Awasthi, Y.C. (2000) Novel function of human RLIP76: ATP-dependent transport of glutathione conjugates and doxorubicin. Biochemistry 39, 9327-9334.
  • 2.Awasthi, S., Singhal, S.S., Srivastava, S.K., Zimniak, P., Bajpai, K.K., Saxena, M., Sharma, R., Ziller, S.A. III, Frenkel, E.P., Singh, S.V., He, N.G. & Awasthi, Y.C. (l994) Adenosine triphosphate-dependent transport of doxorubicin, daunomycin, and vinblastine in human tissues by a mechanism distinct from the P-glycoprotein. J. Clin. Invest. 93, 958-965.
  • 3.Awasthi, S., Singhal, S.S., He, N.G., Chaubey, M., Zimniak, P., Srivastava, S.K., Singh, S.V. & Awasthi, Y.C. (1996) Modulation of doxorubicin cytotoxicity by ethacrynic acid. Int. J. Cancer 68, 333-339.
  • 4.Awasthi, S., Singhal, S.S., Srivastava, S.K., Torman, R.T., Zimniak, P., Bandorowicz- Pikula, J., Singh, S.V., Piper, J.T., Awasthi, Y.C. & Pikula, S. (1998) ATP-dependent human erythrocyte glutathione-conjugate transporter. I. Purification, photoaffinity labeling and kinetic characteristics of ATPase activity. Biochemistry 37, 5231-5238.
  • 5.Awasthi, S., Singhal, S.S., Pikula, S., Piper, J.T., Srivastava, S.K., Torman, R.T., Bandorowicz-Pikula, J., Lin, J.T., Singh, S.V., Zimniak, P. & Awasthi, Y.C. (1998) ATP-dependent human erythrocyte glutathione-conjugate transporter. II. Functional reconstitution of transport activity. Biochemistry 37, 5239-5248.
  • 6.Awasthi, S., Singhal, S.S., Pandya, U., Gopal, S., Zimniak, P., Singh, S.V. & Awasthi, Y.C. (1999) ATP-dependent colchicine transport by human erythrocyte glutathione conjugate transporter. Toxicol. Appl. Pharmacol. 155, 215-226.
  • 7.Sharma, R., Awasthi, S., Zimniak, P. & Awasthi, Y.C. (2000) Transport of glutathione- conjugates in human erythrocytes. Acta Biochim. Polon. 47, 751-762.
  • 8.Jullien-Flores, V., Dorseuil, O., Romero, F., Letourneur, F., Saragosti, S., Berger, R., Tavitian, A, Gacon, G. & Camonis, J.H. (1995) Bridging Ral GTPase to Rho pathways. RLIP76, a Ral effector with CDC42/Rac GTPase-activating protein activity. J. Biol. Chem. 270, 22473-22477.
  • 9.Bauer, B., Mirey, G., Vetter, I.R., Garcia-Ranea, J.A., Valencia, A, Wittinghofer, A., Camonis, J.H. & Cool, R.H. (1999) Effector recognition by the small GTP-binding proteins Ras and Ral. J. Biol. Chem. 274, 17763-17770.
  • 10.Feig, L.A., Urano, T. & Cantor, S. (1996) Evidence for a Ras/Ral signaling cascade. Trends Biochem. Sci. 21, 438-441.
  • 11.Bos, J.L. (1998) All in the family? New insights and questions regarding interconnectivity of Ras, Rap1 and Ral. EMBO J. 17, 6776-6782.
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  • 13.Valencia, A., Chardin, P., Wittinghofer, A. & Sander, C. (1991) The ras protein family: Evolutionary tree and role of conserved amino acids. Biochemistry 30, 4637-4648.
  • 14.Nakashima, S., Morinaka, K., Koyama, S., Ikeda, M., Kishida, M., Okawa, K., Iwamatsu, A., Kishida, S. & Kikuchi, A. (1999) Small G protein Ral and its downstream molecules regulate endocytosis of EGF and insulin receptors. EMBO J. 18, 3629-3642.
  • 15.Quaroni, A. & Paul, E.C. (1999) Cytocentrin is a Ral-binding protein involved in the assembly and function of the mitotic apparatus. J. Cell Sci. 112, 707-718.
  • 16.Monk, T.J., Lau, S.S., Highet, R.J. & Gillette, J.R. (1985) Glutathione conjugates of 2-bromohydroquinone are nephrotoxic. DrugMetab. Dispos. 13, 553-559.
  • 17.Mertens, J.J., Gibson, N.W., Lau, S.S. & Monk, T.J. (1995) Reactive oxygen species and DNA damage in 2-bromo-(glutathion-S-yl) hydroquinone-mediated cytotoxicity. Arch. Biochem. Biophys. 320, 51-58.
  • 18.Bilzer, M., Krauth-Siegel, R.L., Schirmer, R.H., Akerboom, T.P., Sies, H. & Schulz, G.E. (1984) Interaction of a glutathione S-conjugate with glutathione reductase. Kinetic and x-ray crystallographic studies. Eur. J. Biochem. 138, 373-378.
  • 19.Awasthi, S., Srivastava, S.K., Ahmad, F., Ahmad, H. & Ansari, G.A.S. (1993) Interactions of glutathione S-transferase pi with ethacrynic acid and its glutathione conjugate. Biochim. Biophys. Acta 1164, 173-178.
  • 20.Park, S.H. & Weinberg, R.A. (1995) A putative effector of Ral has homology to Rho/Rac GTPase activating proteins. Oncogene 11, 2349-2355.
  • 21.Cantor, S.B., Yrano, T. & Feig, L.A. (1995) Identification and characterization of Ral-binding protein 1 and a potential downstream target of Ral GTPases. Mol. Cell. Biol. 15, 4578-4584.
  • 22.Jullien-Flores, V., Mahe, Y., Mirey, G., Leprince, C., Meunier-Bisceuil, B., Sorkin, A. & Camonis, J.H. (2000) RLIP76, an effector of the GTPase Ral, interacts with the AP2 complex: Involvement of the Ral pathway in receptor endocytosis. J. Cell Sci. 113, 2837-2844.
  • 23.Awasthi, S., Cheng, J., Singhal, S.S., Pandya, U., Sharma, R., Singh, S.V., Zimniak, P. & Awasthi, Y.C. (2001) Functional reassembly of ATP-dependent xenobiotic transport by the N- and C-terminal domains of RLIP76 and identification of ATP binding sequences. Biochemistry 40, 4159-4168.
  • 24.Minamide, L.S. & Bamburg, J.R. (1990) A filter paper dye-binding assay for quantitative determination of protein without interference from reducing agents or detergents. Anal. Biochem. 190, 66-70.
  • 25.Towbin, H., Staehelin, T. & Gordon, J. (1979) Electrophoretic transfer of protein from polyacrylamide gels to nitrocellulose sheets: Procedure and some applications. Proc. Natl. Acad. Sci. U.S.A. 76, 4350-4353.
  • 26.Laemmli, U.K. (1970) Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227, 680-685.
  • 27.Pikula, S., Hayden, J.B., Awasthi, S., Awasthi, Y.C. & Zimniak, P. (1994) Organic anion-transporting ATPase of rat liver. II. Functional reconstitution of active transport and regulation by phosphorylation. J. Biol. Chem. 269, 27574-27579.
  • 28.Sharma, R., Gupta, S., Singh, S.V., Medh, R.D., Ahmad, H., LaBelle, E.F. & Awasthi, Y.C. (1990) Purification and characterization of dinitrophenyl glutathione ATPase of human erythrocytes and its expression in other tissues. Biochem. Biophys. Res. Commun. 171, 155-161.
  • 29.Awasthi, Y.C., Singhal, S.S., Gupta, S., Ahmad, H., Zimniak, P., Radominska, A., Lester, R. & Sharma, R. (1991) Purification and characterization of an ATPase from human liver which catalyzes ATP hydrolysis in the presence of the conjugates of bilirubin bile acids and glutathione. Biochem. Biophys. Res. Commun. 175, 1090-1096.
  • 30.Singhal, S.S., Sharma, R., Gupta, S., Ahmad, H., Zimniak, P., Radominska, A., Lester, R. & Awasthi, Y.C. (1991) The anionic conjugates of bilirubin and bile acids stimulate ATP hydrolysis by S-(dinitrophenyl) glutathione ATPase of human erythrocyte. FEBSLett. 281, 255-257.
  • 31.Saxena, M., Singhal, S.S., Awasthi, S., Singh, S.V., LaBelle, E.F., Zimniak, P. & Awasthi, Y.C. (1992) Dinitrophenyl S-glutathione ATPase purified from human muscle catalyzes ATP hydrolysis in the presence of leukotrienes. Arch. Biochem. Biophys. 298, 231-237.

Typ dokumentu

Bibliografia

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Identyfikator YADDA

bwmeta1.element.agro-article-96f82138-55ea-40f3-8e24-a677f751c119
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