Registro:

Referencias:

• Sukharev, S., Corey, D.P., Mechanosensitive channels: multiplicity of families and gating paradigms (2004) Sci Signal, p. re4
• Booth, I.R., Blount, P., The MscS and MscL families of mechanosensitive channels act as microbial emergency release valves (2012) J Bacteriol, 194, pp. 4802-4809
• Booth, I.R., Louis, P., Managing hypoosmotic stress: aquaporins and mechanosensitive channels in Escherichia coli (1999) Curr Opin Microbiol, 2, pp. 166-169
• Wan, X., Steudle, E., Hartung, W., Gating of water channels (aquaporins) in cortical cells of young corn roots by mechanical stimuli (pressure pulses): effects of ABA and of HgCl 2 (2004) J Exp Bot, 55, pp. 411-422
• Törnroth-Horsefield, S., Hedfalk, K., Fischer, G., Lindkvist-Petersson, K., Neutze, R., Structural insights into eukaryotic aquaporin regulation (2010) FEBS Lett, 584, pp. 2580-2588
• Conner, A.C., Bill, R.M., Conner, M.T., An emerging consensus on aquaporin translocation as a regulatory mechanism (2013) Mol Membr Biol, 30, pp. 101-112
• Chevalier, A.S., Chaumont, F., Trafficking of plant plasma membrane aquaporins: multiple regulation levels and complex sorting signals (2015) Plant Cell Physiol, 56, pp. 819-829
• Sasaki, S., Yui, N., Noda, Y., Actin directly interacts with different membrane channel proteins and influences channel activities: AQP2 as a model (2014) Biochim. Biophys Acta - Biomembr, 1838, pp. 514-520
• Jozefkowicz, C., Rosi, P., Sigaut, L., Soto, G., Pietrasanta, L.I., Amodeo, G., Alleva, K., Loop a is critical for the functional interaction of two Beta vulgaris PIP aquaporins (2013) PLoS One, 8
• Jozefkowicz, C., Sigaut, L., Scochera, F., Soto, G., Ayub, N., Pietrasanta, L.I., Amodeo, G., Alleva, K., PIP water transport and its pH dependence are regulated by tetramer stoichiometry (2016) Biophys J, 110, pp. 1312-1321
• Soveral, G., Madeira, A., Loureiro-Dias, M.C., Moura, T.F., Membrane tension regulates water transport in yeast (2008) Biochim Biophys Acta - Biomembr, 1778, pp. 2573-2579
• Ye, Q., Wiera, B., Steudle, E., A cohesion/tension mechanism explains the gating of water channels (aquaporins) in Chara internodes by high concentration (2004) J Exp Bot, 55, pp. 449-461
• Ozu, M., Dorr, R.A., Teresa Politi, M., Parisi, M., Toriano, R., Water flux through human aquaporin 1: inhibition by intracellular furosemide and maximal response with high osmotic gradients (2011) Eur Biophys J, 40, pp. 737-746
• Leitão, L., Prista, C., Loureiro-Dias, M.C., Moura, T.F., Soveral, G., The grapevine tonoplast aquaporin TIP2;1 is a pressure gated water channel (2014) Biochem Biophys Res Commun, 450, pp. 289-294
• Soveral, G., Macey, R.I., Moura, T.F., Membrane stress causes inhibition of water channels in brush border membrane vesicles from kidney proximal tubule (1997) Biol Cell, 89, pp. 275-282
• Niemietz, C.M., Tyerman, S.D., Characterization of water channels in wheat root membrane vesicles (1997) Plant Physiol, 115, pp. 561-567
• Ozu, M., Dorr, R.A., Gutiérrez, F., Politi, M.T., Toriano, R., Human AQP1 is a constitutively open channel that closes by a membrane-tension-mediated mechanism (2013) Biophys J, 104, pp. 85-95
• Dumont, J.N., Oogenesis in Xenopus laevis (Daudin). I. Stages of oocyte development in laboratory maintained animals (1972) J Morphol, 136, pp. 153-179
• Preston, G.M., Carroll, T.P., Guggino, W.B., Agre, P., Appearance of water channels in Xenopus oocytes expressing red cell CHIP28 protein (1992) Science, 256, pp. 385-387
• Ozu, M., Dorr, R., Parisi, M., New method to measure water permeability in emptied-out Xenopus oocytes controlling conditions on both sides of the membrane (2005) J Biochem Biophys Methods, 63, pp. 187-200
• Dorr, R., Ozu, M., Parisi, M., Simple and inexpensive hardware and software method to measure volume changes in Xenopus oocytes expressing aquaporins (2007) J Neurosci Methods, 161, pp. 301-305
• Cosgrove, D., Steudle, E., Water relations of growing pea epicotyl segments (1981) Planta, 153, pp. 343-350
• Iscla, I., Blount, P., Sensing and responding to membrane tension: the bacterial MscL channel as a model system (2012) Biophys J, 103, pp. 169-174
• Arnold, K., Bordoli, L., Kopp, J., Schwede, T., The SWISS-MODEL workspace: a web-based environment for protein structure homology modelling (2006) Bioinformatics, 22, pp. 195-201
• Törnroth-Horsefield, S., Wang, Y., Hedfalk, K., Johanson, U., Karlsson, M., Tajkhorshid, E., Neutze, R., Kjellbom, P., Structural mechanism of plant aquaporin gating (2006) Nature, 439, pp. 688-694
• Kirscht, A., Kaptan, S.S., Bienert, G.P., Chaumont, F., Nissen, P., de Groot, B.L., Kjellbom, P., Johanson, U., Crystal structure of an ammonia-permeable aquaporin (2016) PLoS Biol, 14
• Humphrey, W., Dalke, A., Schulten, K., VMD: Visual molecular dynamics (1996) J Mol Graph, 14, pp. 33-38
• Kelly, S.M., Jia, Y.L., Macklem, P.T., Measurement of elastic properties of Xenopus oocytes (1997) Comp Biochem Physiol, 118, pp. 607-613
• Maurel, C., Boursiac, Y., Luu, D.-T., Santoni, V., Shahzad, Z., Verdoucq, L., Aquaporins in plants (2015) Physiol Rev, 95, pp. 1321-1358
• Maurel, C., Plant aquaporins: novel functions and regulation properties (2007) FEBS Lett, 581, pp. 2227-2236
• Soto, G., Alleva, K., Amodeo, G., Muschietti, J., Ayub, N.D., New insight into the evolution of aquaporins from flowering plants and vertebrates: orthologous identification and functional transfer is possible (2012) Gene, 503, pp. 165-176
• Neuhaus, H.E., Trentmann, O., Regulation of transport processes across the tonoplast (2014) Front Plant Sci, 5, p. 460
• Zhang, C., Hicks, G.R., Raikhel, N.V., Plant vacuole morphology and vacuolar trafficking (2014) Front Plant Sci, 5, p. 476
• Ivakov, A., Persson, S., Plant cell shape: modulators and measurements (2013) Front Plant Sci, 4, pp. 1-13
• Martinac, B., The ion channels to cytoskeleton connection as potential mechanism of mechanosensitivity (2014) Biochim Biophys Acta - Biomembr, 1838, pp. 682-691
• Sukharev, S., Sachs, F., Molecular force transduction by ion channels – diversity and unifying principles (2012) J Cell Sci, 125, pp. 3075-3083
• Sachs, F., Stretch-activated ion channels: What are they? (2010) Physiology, 25, pp. 50-56
• Peyronnet, R., Tran, D., Girault, T., Frachisse, J.-M., Mechanosensitive channels: feeling tension in a world under pressure (2014) Front. Plant Sci, 5, p. 558
• Alexandre, J., Lassalles, J.-P., Hydrostatic and osmotic pressure activated channel in plant vacuole (1991) Biophys J, 60, pp. 1326-1336
• Anishkin, A., Loukin, S.H., Teng, J., Kung, C., Feeling the hidden mechanical forces in lipid bilayer is an original sense (2014) Proc Natl Acad Sci USA, 111, pp. 7898-7905
• Teng, J., Loukin, S., Anishkin, A., Kung, C., The force-from-lipid (FFL) principle of mechanosensitivity, at large and in elements (2014) Pflügers Arch - Eur J Physiol, 467, pp. 27-37
• Tong, J., Briggs, M.M., McIntosh, T.J., Water permeability of Aquaporin-4 channel depends on bilayer composition, thickness, and elasticity (2012) Biophys J, 103, pp. 1899-1908
• Stansfeld, P.J., Jefferys, E.E., Sansom, M.S.P., Multiscale simulations reveal conserved patterns of lipid interactions with aquaporins (2013) Structure, 21, pp. 810-819
• Russ, W.P., Engelman, D.M., The GxxxG motif: a framework for transmembrane helix-helix association (2000) J Mol Biol, 296, pp. 911-919
• Balleza, D., Toward understanding protocell mechanosensation (2011) Origins of Life and Evolution of Biospheres, 41, pp. 281-304
• Perozo, E., Rees, D.C., Structure and mechanism in prokaryotic mechanosensitive channels (2003) Curr Opin Struct Biol, 13, pp. 432-442
• Fujiyoshi, Y., Mitsuoka, K., de Groot, B.L., Philippsen, A., Grubmüller, H., Agre, P., Engel, A., Structure and function of water channels (2002) Curr Opin Struct Biol, 12, pp. 509-515
• Perez Di Giorgio, J., Soto, G., Alleva, K., Jozefkowicz, C., Amodeo, G., Muschietti, J.P., Ayub, N.D., Prediction of aquaporin function by integrating evolutionary and functional analyses (2014) J Membr Biol, 247, pp. 107-125

Citas:

---------- APA ----------

---------- CHICAGO ----------

---------- MLA ----------

---------- VANCOUVER ----------