Structure-Function Relations of MscS

Current Topics in Membranes

Volumn 58, Issue , 2007, Pages 269-294

  Booth, Ian R ^a   Edwards, Michelle D ^a   Miller, Samantha ^a   Li, Chan ^a   Black, Susan ^a   Bartlett, Wendy ^a   Schumann, Ulrike ^a  

^a UNIVERSITY OF ABERDEEN   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 34047115325     PISSN: 10635823     EISSN: None     Source Type: Book Series    
DOI: 10.1016/S1063-5823(06)58010-X     Document Type: Review

References (56)

1. Akitake B., Anishkin A., and Sukharev S. The "dashpot" mechanism of stretch-dependent gating in MscS. J. Gen. Physiol. 125 (2005) 143-154
2. Anishkin A., and Sukharev S. Water dynamics and dewetting transition in the small mechanosensitive channel MscS. Biophys. J. 86 (2004) 2883-2895
3. Anishkin A., Chiang C.S., and Sukharev S. Gain-of-function mutations reveal expanded intermediate states and a sequential action of two gates in MscL. J. Gen. Physiol. 125 (2005) 155-170
4. Bass R.B., Strop P., Barclay M., and Rees D.C. Crystal structure of Escherichia coli MscS, a voltage-modulated and mechanosensitive channel. Science 298 (2002) 1582-1587
5. Batiza A.F., Kuo M.M.C., Yoshimura K., and Kung C. Gating the bacterial mechanosensitive channel MscL in vivo. Proc. Natl. Acad. Sci. USA 99 (2002) 5643-5648
6. Berrier C., Coulombe A., Szabo I., Zoratti M., and Ghazi A. Gadolinium ion inhibits loss of metabolites induced by osmotic shock and large stretch-activated channels in bacteria. Eur. J. Biochem. 206 (1992) 559-565
7. Berrier C., Besnard M., Ajouz B., Coulombe A., and Ghazi A. Multiple mechanosensitive ion channels from Escherichia coli, activated at different thresholds of applied pressure. J. Membr. Biol. 151 (1996) 175-187
8. Blount P., Sukharev S.I., Moe P.C., Nagle S.K., and Kung C. Towards an understanding of the structural and functional properties of MscL, a mechanosensitive channel in bacteria. Biol. Cell 87 (1996) 1-8
9. Blount P., Sukharev S.I., Schroeder M.J., Nagle S.K., and Kung C. Single residue substitutions that change the gating properties of a mechanosensitive channel in Escherichia coli. Proc. Natl. Acad. Sci. USA 93 (1996) 11652-11657
10. Blount P., Schroeder M.J., and Kung C. Mutations in a bacterial mechanosensitive channel change the cellular response to osmotic stress. J. Biol. Chem. 272 (1997) 32150-32157
11. Booth I.R. Regulation of cytoplasmic Ph in bacteria. Microbiol. Rev. 49 (1985) 359-378
12. Booth I.R., Cairney J., Sutherland L., and Higgin C.F. Enteric bacteria and osmotic stress: An integrated homeostatic system. Soc. Appl. Bacteriol. Symp. Ser. 17 (1988) 35S-49S
13. + in Escherichia coli. J. Bacteriol. 186 (2004) 4238-4245
14. Chang G., Spencer R.H., Lee A.T., Barclay M.T., and Rees D.C. Structure of the MscL homolog from Mycobacterium tuberculosis: A gated mechanosensitive ion channel. Science 282 (1998) 2220-2226
15. + conduction and selectivity. Science 280 (1998) 69-77
16. Dutzler R., Campbell E.B., Cadene M., Chait B.T., and MacKinnon R. X-ray structure of a CIC chloride channel at 3. 0 angstrom reveals the molecular basis of anion selectivity. Nature 415 (2002) 287-294
17. Edwards M.D., Booth I.R., and Miller S. Gating the mechanosensitive channels: MscS a new paradigm?. Curr. Opin. Microbiol. 7 2 (2004) 163-167
18. Edwards M.D., Li Y., Kim S., Miller S., Bartlett W., Black S., Dennison S., Iscla I., Blount P., Bowie J.U., and Booth I.R. Pivotal role of the glycine-rich TM3 helix in gating the MscS mechanosensitive channel. Nat. Struct. Mol. Biol. 12 (2005) 113-119
19. Folgering J.H., Moe P.C., Schuurman-Wolters G.K., Blount P., and Poolman B. Lactococcus lactis uses MscL as its principal mechanosensitive channel. J. Biol. Chem. 280 (2005) 8784-8792
20. Grajkowski W., Kubalski A., and Koprowski P. Surface changes of the mechanosensitive channel MscS upon its activation, inactivation, and closing. Biophys. J. 88 (2005) 3050-3059
21. Haswell E.S., and Meyerowitz E.M. MscS-like proteins control plastid size and shape in Arabidopsis thaliana. Curr. Biol. 16 (2006) 1-11
22. Hengge-Aronis R. Back to log phase: Sigma S as a global regulator in the osmotic control of gene expression in Escherichia coli. Mol. Microbiol. 21 (1996) 887-893
23. Hengge-Aronis R., Lange R., Henneberg N., and Fischer D. Osmotic regulation of rpoS-dependent genes in Escherichia coli. J. Bacteriol. 175 (1993) 259-265
24. Klauck E., Bohringer J., and Hengge-Aronis R. The LysR-like regulator LeuO in Escherichia coli is involved in the translational regulation of rpoS by affecting the expression of the small regulatory DsrA-RNA. Mol. Microbiol. 25 (1997) 559-569
25. Kloda A., and Martinac B. Mechanosensitive channels in Archaea. Cell Biochem. Biophys. 34 (2001) 349-381
26. Kloda A., and Martinac B. Structural and functional differences between two homologous mechanosensitive channels of Methanococcus jannaschii. EMBO J. 20 (2001) 1888-1896
27. Koprowski P., and Kubalski A. Voltage-independent adaptation of mechanosensitive channels in Escherichia coli protoplasts. J. Membr. Biol. 164 (1998) 253-262
28. Koprowski P., and Kubalski A. C-termini of the Escherichia coli mechanosensitive ion channel (MscS) move apart upon the channel opening. J. Biol. Chem. 278 (2003) 11237-11245
29. Kung C., and Blount P. Channels in microbes: So many holes to fill. Mol. Microbiol. 53 (2004) 373-380
30. Levina N., Totemeyer S., Stokes N.R., Louis P., Jones M.A., and Booth I.R. Protection of Escherichia coli cells against extreme turgor by activation of MscS and MscL mechanosensitive channels: Identification of genes required for MscS activity. EMBO J. 18 (1999) 1730-1737
31. Li Y., Moe P.C., Chandrasekaran S., Booth I.R., and Blount P. Ionic regulation of MscK, a mechanosensitive channel from Escherichia coli. EMBO J. 21 (2002) 5323-5330
32. Martinac B., Buehner M., Delcour A.H., Adler J., and Kung C. Pressure-sensitive ion channel in Escherichia coli. Proc. Natl. Acad. Sci. USA 84 (1987) 2297-2301
33. Martinac B., Adler J., and Kung C. Mechanosensitive ion channels of E. coli activated by amphipaths. Nature 348 (1990) 261-263
34. Martz E. Protein explorer: Easy yet powerful macromolecular visualization. Trends Biochem. Sci. 27 (2002) 107-109
35. McLaggan D., Jones M.A., Gouesbet G., Levina N., Lindey S., Epstein W., and Booth I.R. Analysis of the kefA2 mutation suggests that KefA is a cation-specific channel involved in osmotic adaptation in Escherichia coli. Mol. Microbiol. 43 (2002) 521-536
36. Miller S., Bartlett W., Chandrasekaran S., Simpson S., Edwards M., and Booth I.R. Domain organization of the MscS mechanosensitive channel of Escherichia coli. EMBO J. 22 (2003) 36-46
37. Miller S., Edwards M.D., Ozdemir C., and Booth I.R. The closed structure of the MscS mechanosensitive channel-Cross-linking of single cysteine mutants. J. Biol. Chem. 278 (2003) 32246-32250
38. Nguyen T., Clare B., Guo W., and Martinac B. The effects of parabens on the mechanosensitive channels of E. coli. Eur. Biophys. J. 34 (2005) 389-395
39. Nottebrock D., Meyer U., Kramer R., and Morbach S. Molecular and biochemical characterization of mechanosensitive channels in Corynebacterium glutamicum. FEMS Microbiol. Lett. 218 (2003) 305-309
40. Okada K., Moe P.C., and Blount P. Functional design of bacterial mechanosensitive channels. Comparisons and contrasts illuminated by random mutagenesis. J. Biol. Chem. 277 (2002) 27682-27688
41. Ou X., Blount P., Hoffman R.J., and Kung C. One face of a transmembrane helix is crucial in mechanosensitive channel gating. Proc. Natl. Acad. Sci. USA 95 (1998) 11471-11475
42. Perozo E., Kloda A., Cortes D.M., and Martinac B. Site-directed spin-labeling analysis of reconstituted MscL in the closed state. J. Gen. Physiol. 118 (2001) 193-206
43. Perozo E., Cortes D.M., Sompornpisut P., Kloda A., and Martinac B. Open channel structure of MscL and the gating mechanism of mechanosensitive channels. Nature 418 (2002) 942-948
44. Perozo E., Kloda A., Cortes D.M., and Martinac B. Physical principles underlying the transduction of bilayer deformation forces during mechanosensitive channel gating. Nat. Struct. Biol. 9 (2002) 696-703
45. Pivetti C.D., Yen M.R., Miller S., Busch W., Tseng Y.H., Booth I.R., and Saier M.H. Two families of mechanosensitive channel proteins. Microbiol. Mol. Biol. Rev. 67 (2003) 66-85
46. Ruffert S., Berrier C., Kramer R., and Ghazi A. Identification of mechanosensitive ion channels in the cytoplasmic membrane of Corynebacterium glutamicum. J. Bacteriol. 181 (1999) 1673-1676
47. Schellhorn H.E., Audia J.P., Wei L.I.C., and Chang L. Identification of conserved, RpoS-dependent stationary-phase genes of Escherichia coli. J. Bacteriol. 180 (1998) 6283-6291
48. Schumann U., Edwards M.D., Li C., and Booth I.R. The conserved carboxy-terminus of the MscS mechanosensitive channel is not essential but increases stability and activity. FEBS Lett. 572 (2004) 233-237
49. Shapovalov G., and Lester H.A. Gating transitions in bacterial ion channels measured at 3 microns resolution. J. Gen. Physiol. 124 (2004) 151-161
50. Spronk S.A., Elmore D.E., and Dougherty D.A. Voltage-dependent hydration and conduction properties of the hydrophobic pore of the mechanosensitive channel of small conductance. Biophys. J. 90 (2006) 3555-3569
51. Stokes N.R., Murray H.D., Subramaniam C., Gourse R.L., Louis P., Bartlett W., Miller S., and Booth I.R. A role for mechanosensitive channels in survival of stationary phase: Regulation of channel expression by RpoS. Proc. Natl. Acad. Sci. USA 100 (2003) 15959-15964
52. Sukharev S. Purification of the small mechanosensitive channel of Escherichia coli (MscS): The subunit structure, conduction, and gating characteristics in liposomes. Biophys. J. 83 (2002) 290-298
53. Sukharev S.I., Martinac B., Arshavsky V.Y., and Kung C. Two types of mechanosensitive channels in the Escherichia coli cell envelope: Solubilization and functional reconstitution. Biophys. J. 65 (1993) 177-183
54. Toro I., Basquin J., Teo-Dreher H., and Suck D. Archaeal Sm proteins form heptameric and hexameric complexes: Crystal structures of the Sm1 and Sm2 proteins from the hyperthermophile Archaeoglobus fulgidus. J. Mol. Biol. 320 (2002) 129-142
55. Touze T., Gouesbet G., Bolangiu C., Jebbar M., Bonnassie S., and Blanco C. Glycine betaine loses its osmoprotective activity in a bspA strain of Erwinia chrysanthemi. Mol. Microbiol. 42 (2001) 87-99
56. + channel-Fab complex at 2. 0 angstrom resolution. Nature 414 (2001) 43-48