ライフサイエンスコーパス: cytoplasmic membrane

1 , the TLR2 agonists, from the staphylococcal cytoplasmic membrane.

2 histidines in the extracellular half of the cytoplasmic membrane.

3 llowed by alpha helices that extend into the cytoplasmic membrane.

4 nt as one molecule for every 91 nm(2) in the cytoplasmic membrane.

5 bly into a functional complex located at the cytoplasmic membrane.

6 s a protective mesh-like sacculus around the cytoplasmic membrane.

7 d dimeric proteins across the tightly sealed cytoplasmic membrane.

8 is its ability to conduct protons across the cytoplasmic membrane.

9 c oxidase lie on the periplasmic side of the cytoplasmic membrane.

10 determine the pH gradient across the E. coli cytoplasmic membrane.

11 access to DNA receptors associated with the cytoplasmic membrane.

12 f a galactopyranoside and an H(+) across the cytoplasmic membrane.

13 pid II during transport across the bacterial cytoplasmic membrane.

14 leton influences fluorescent staining of the cytoplasmic membrane.

15 y electrochemical Na(+) potential across its cytoplasmic membrane.

16 omoting its lipid-mediated attachment to the cytoplasmic membrane.

17 t parallel with FtsZ polymers underneath the cytoplasmic membrane.

18 II, and this complex also forms pores in the cytoplasmic membrane.

19 hinery, which transports proteins across the cytoplasmic membrane.

20 th ubiquinone to pump sodium ions across the cytoplasmic membrane.

21 on of proteins across and into the bacterial cytoplasmic membrane.

22 system is activated by events affecting the cytoplasmic membrane.

23 n bilayers closest in composition to E. coli cytoplasmic membrane.

24 rt of unfolded precursor proteins across the cytoplasmic membrane.

25 ly folded proteins across the tightly sealed cytoplasmic membrane.

26 and are derived from the OM rather than the cytoplasmic membrane.

27 ructural motif that targets a protein to the cytoplasmic membrane.

28 volved in the flipping of lipid A across the cytoplasmic membrane.

29 y mannosyltransferase enzymes located at the cytoplasmic membrane.

30 inone coupled with proton pumping across the cytoplasmic membrane.

31 ith the negative immune regulator SRFR1 at a cytoplasmic membrane.

32 le transertion of membrane proteins into the cytoplasmic membrane.

33 polysialic acid (NmC PST) is located in the cytoplasmic membrane.

34 ting it without contamination from the inner cytoplasmic membrane.

35 ic pore for transport of NH(4)(+) across the cytoplasmic membrane.

36 lacking an OM, MRL-494 lethally disrupts the cytoplasmic membrane.

37 actions which include the outer membrane and cytoplasmic membrane.

38 plasm and processed into mature forms on the cytoplasmic membrane.

39 substantial pressure differential across the cytoplasmic membrane.

40 00-superfamily protein substrates across the cytoplasmic membrane.

41 f the peptidoglycan layer that surrounds the cytoplasmic membrane.

42 organisms as they affect the function of the cytoplasmic membrane.

43 a coli periplasm and that it depolarizes the cytoplasmic membrane.

44 les that originate from invaginations of the cytoplasmic membrane.

45 ty of three enzymes that are embedded in the cytoplasmic membrane.

46 transfer to PBP1b after transport across the cytoplasmic membrane.

47 h thiolate ligands through a model bacterial cytoplasmic membrane.

48 n machine called the divisome that spans the cytoplasmic membrane.

49 ly enlarged and convoluted, and an energized cytoplasmic membrane.

50 h-like sacculus that surrounds the bacterial cytoplasmic membrane.

51 translocation of the Hsa adhesin across the cytoplasmic membrane.

52 efficient transit through both the outer and cytoplasmic membranes.

53 r at the interface between the thylakoid and cytoplasmic membranes.

54 e sequence complement on their cell walls or cytoplasmic membranes.

55 tor-containing cargo proteins over bacterial cytoplasmic membranes.

56 inetic study of drug entry through bacterial cytoplasmic membranes.

57 tem comprising outer, cytoplasmic, and inner cytoplasmic membranes.

58 GLa using lipid-only mimics of Gram-negative cytoplasmic membranes.

59 phosphatidylglycerol mimics of Gram-negative cytoplasmic membranes.

60 taining species can permeate readily through cytoplasmic membranes.

61 ns were shown to accumulate in thylakoid and cytoplasmic membranes.

62 pids from the outer leaflet of the OM to the cytoplasmic membrane (4) .

63 peptidoglycan precursor lipid II across the cytoplasmic membrane(7,8).

64 optimal interactions with the ligand and the cytoplasmic membrane ABC transporter (FepCD), respective

65 tion, dynamic shrinking and extension of the cytoplasmic membrane accompanied by lysis and cell death

66 s also required for the stabilization of the cytoplasmic membrane and as a cofactor for essential enz

67 uclear cyclin D1, which bound ERalpha at the cytoplasmic membrane and augmented AKT phosphorylation (

68 negative bacteria are surrounded by an inner cytoplasmic membrane and by an outer membrane, which ser

69 om Escherichia coli resides in the bacterial cytoplasmic membrane and catalyzes the two-electron oxid

70 to extracytoplasmic stresses that damage the cytoplasmic membrane and enable cells to repair their me

71 ids alters the biochemical properties of the cytoplasmic membrane and enables bacteria to adapt to ch

72 pts the proton motive force at the bacterial cytoplasmic membrane and extends animal survival during

73 athway transports folded proteins across the cytoplasmic membrane and has been implicated in virulenc

74 Additionally, FraG was located close to the cytoplasmic membrane and in the heterocyst neck, using i

75 Cruzipain is found both on the cytoplasmic membrane and in the internal lysosomal struc

76 ocket is where an alpha-helix runs along the cytoplasmic membrane and interacts with a neighboring su

77 n transport systems found in the prokaryotic cytoplasmic membrane and is conserved in the thylakoid m

78 (Tat) transports folded proteins across the cytoplasmic membrane and is critical to virulence in Sal

79 r its release from noncentral regions of the cytoplasmic membrane and its subsequent relocation to mi

80 raction of LPS from the outer leaflet of the cytoplasmic membrane and its transport across the cell e

81 ng infection, viral capsids assembled on the cytoplasmic membrane and moved to the surface of the com

82 uire holins and endolysins, which attack the cytoplasmic membrane and peptidoglycan, respectively.

83 chemotactic responses by diffusing into the cytoplasmic membrane and perturbing the structural stabi

84 To fortify their cytoplasmic membrane and protect it from osmotic rupture

85 d fluorophores with rapid diffusion into the cytoplasmic membrane and sequestration inside the lysoso

86 tly or indirectly interacts with KinD in the cytoplasmic membrane and that this interaction is requir

87 ll as MscK distribute homogeneously over the cytoplasmic membrane and the lateral diffusion of the ch

88 locates folded proteins across the bacterial cytoplasmic membrane and the plant thylakoid membrane.

89 ports folded proteins across the prokaryotic cytoplasmic membrane and the plant thylakoid membrane.

90 nsports folded proteins across the bacterial cytoplasmic membrane and the plant thylakoid membrane.

91 and owing to the semipermeable nature of the cytoplasmic membrane and the semielastic properties of t

92 port of folded proteins across the bacterial cytoplasmic membrane and the thylakoid membrane in plant

93 nsports folded proteins across the bacterial cytoplasmic membrane and the thylakoid membranes of plan

94 t relocation of Vipp1 to the vicinity of the cytoplasmic membrane and the thylakoid membranes.

95 , is synthesized in the inner leaflet of the cytoplasmic membrane and then translocated across the bi

96 l domain of Rz near the outer leaflet of the cytoplasmic membrane and were not allele specific.

97 induce pores, or otherwise permeabilise the cytoplasmic membrane and, as a result, induce cell death

98 sms or receptor-independent diffusion across cytoplasmic membranes and are utilized as nutrients, bui

99 rized the attack of AMPs on Escherichia coli cytoplasmic membranes and directly compared this action

100 rgely responsible for recruitment of pUL7 to cytoplasmic membranes and into the virion tegument.

101 on or blocking of entry mediators, occurs in cytoplasmic membranes and not in cell surface membranes

102 synthesized by enzymes located in the inner (cytoplasmic) membrane and are then translocated to the c

103 NH3 equilibrates across the cytoplasmic membrane, and glutamine synthetase does not

104 ght up in multiple colors HA-tagged nuclear, cytoplasmic, membrane, and mitochondrial proteins in div

105 ds that accumulated were frequently bound to cytoplasmic membranes, apparently immobilized in interme

106 normally used to translocate proteins across cytoplasmic membranes, are a vast family of natural FPR

107 by a dramatic local outward curvature of the cytoplasmic membrane as it fuses with the phage tail tip

108 Cytoplasmic membrane-associated DNA (cmDNA) is a species

109 Importantly, we found there is a special cytoplasmic membrane-associated transcription system in

110 cytosolic proteins FeoA and FeoC and a large cytoplasmic-membrane-associated protein FeoB, which has

111 It forms filaments under the cytoplasmic membrane at the division site where, togethe

112 d but not sufficient to compartmentalize the cytoplasmic membrane at the division site.

113 Escherichia coli SecA binds to cytoplasmic membranes at SecYEG high affinity sites and

114 c myristoylation and Src localization to the cytoplasmic membrane, attenuating Src-mediated oncogenic

115 inked precursors at the inner surface of the cytoplasmic membrane before being translocated across th

116 ell as the cis (vesicle membrane) and trans (cytoplasmic membrane) binding of its two C2 domains.

117 l to several respiratory pathways is CymA, a cytoplasmic membrane-bound tetraheme c-type cytochrome t

118 nd fully occluded cavity at the level of the cytoplasmic membrane boundary, with no ligand bound.

119 for energy production and biogenesis of the cytoplasmic membrane, but they also enhance cellular sig

120 are joined at the extracellular side of the cytoplasmic membrane by a mechanism involving a membrane

121 tion to Fe(2+) prior to traversal across the cytoplasmic membrane by FeoAB.

122 into a proto-ring structure, tethered to the cytoplasmic membrane by FtsA and ZipA.

123 nked PG precursor called lipid II across the cytoplasmic membrane by interfering with the activity of

124 ery and that RNase II is associated with the cytoplasmic membrane by its amino-terminal amphipathic h

125 ell division protein FtsZ is anchored to the cytoplasmic membrane by the action of the bitopic membra

126 ns, such as PAO1, AlgU is sequestered to the cytoplasmic membrane by the anti-sigma factor MucA that

127 Within 30 s of permeabilization of the cytoplasmic membrane by the cationic AMP CM15 [combining

128 PG precursors are translocated across the cytoplasmic membrane by the lipid carrier undecaprenyl p

129 ia, the translocation of proteins across the cytoplasmic membrane by the Sec machinery requires the A

130 tigated the physical properties of bacterial cytoplasmic membranes by applying the method of micropip

131 show penetration of the ARMAN cell wall and cytoplasmic membranes by protuberances extended from cel

132 to GM1-rich, liquid-ordered lipid domains on cytoplasmic membranes by using unroofed cells, which enc

133 Because PG completely encases the cytoplasmic membrane, cleavage of peptide cross-links is

134 ition to distinguishing invaginations of the cytoplasmic membrane (CM) and interconnected vesicular s

135 In Escherichia coli, the integral cytoplasmic membrane (CM) proteins TonB, ExbB, and ExbD

136 y virions leading to their accumulation in a cytoplasmic membrane compartment.

137 ribosome radial distributions extend to the cytoplasmic membrane, consistent with the transertion hy

138 ive Escherichia coli to demonstrate that its cytoplasmic membrane contains microdomains with distinct

139 the proton gradient across the cell wall and cytoplasmic membrane controls Mg(2+) transport into the

140 .1 x 10(5) CFU/mg) via growth inhibition and cytoplasmic membrane damage.

141 oxvirus double-stranded DNA genome occurs in cytoplasmic membrane-delimited factories.

142 We observed immediate cytoplasmic membrane depolarization, not seen with enter

143 cquire their final envelopes by budding into cytoplasmic membranes derived from the trans-Golgi netwo

144 3D analysis revealed cytoplasmic membranes directly adjacent to NE holes cont

145 Analysis of cytoplasmic membrane fatty acids (CMFAs) in acid-adapted

146 how this sulfur is activated and crosses the cytoplasmic membrane for further oxidation to sulfite by

147 ial flippase that translocates it across the cytoplasmic membrane for PG polymerization is unclear.

148 All positive-sense RNA viruses modify host cytoplasmic membranes for viral replication complex form

149 scribed the isolation of a virion-associated cytoplasmic membrane fraction from HSV-infected cells.

150 ges in lateral tension in the bilayer of the cytoplasmic membrane generated by rapid water flow into

151 lae (h-caveolae) form by budding in from the cytoplasmic membrane, generating a membrane domain with

152 transport, implying the existence of another cytoplasmic membrane Hn transporter.

153 associated with DNA translocation across the cytoplasmic membrane (i.e., pilX, comA) did not exhibit

154 adherin and beta-catenin on endothelial cell cytoplasmic membranes, (iii) chemotaxis towards chemoatt

155 that the viral membrane fuses with the host cytoplasmic membrane in a process mediated by VP5.

156 etory and outer membrane proteins across the cytoplasmic membrane in bacteria.

157 t ferries cell wall intermediates across the cytoplasmic membrane in bacteria.

158 the outer membrane or cell wall and (b) the cytoplasmic membrane in case of a cytoplasmic location o

159 RNA processing and decay and tethers to the cytoplasmic membrane in Escherichia coli; however, the f

160 y dissipating the proton motive force of the cytoplasmic membrane in P. aeruginosa.

161 pendent protein translocation pathway across cytoplasmic membranes in bacteria.

162 are phage-encoded proteins that connect the cytoplasmic membrane (inner membrane, IM) and the OM.

163 endent outer membrane receptor (PcuB), and a cytoplasmic membrane-integral protein (PcuE).

164 ains the so-called common region (CR) at the cytoplasmic/membrane interface still has the ability to

165 rerequisite for its translocation across the cytoplasmic membrane into the bacterial periplasm.

166 d proteins are first translocated across the cytoplasmic membrane into the inner wall zone.

167 The bacterial cytoplasmic membrane is a principal site of protein tran

168 Protein translocation across the bacterial cytoplasmic membrane is an essential process catalyzed p

169 Protein translocation across the cytoplasmic membrane is an essential process in all bact

170 The bacterial cytoplasmic membrane is composed of roughly equal propor

171 adial extension of ribosomes and RNAP to the cytoplasmic membrane is consistent with the hypothesis o

172 that controlled AsIII trafficking across the cytoplasmic membrane is important to a process understoo

173 ings strongly suggest that disruption of the cytoplasmic membrane is not the growth-halting mechanism

174 The cytoplasmic membrane is probably the most important phys

175 ation of the amphipathic lipid II across the cytoplasmic membrane is required for subsequent incorpor

176 Val-4830-Val-4841) that lies parallel to the cytoplasmic membrane leaflet.

177 Cellular RNAs often colocalize with cytoplasmic, membrane-less ribonucleoprotein (RNP) granu

178 ter membrane is much faster than through the cytoplasmic membrane, likely reflecting the effectivenes

179 EsaE has a dual cytoplasmic/membrane localization, and membrane-bound Es

180 idase (COX) and quinol oxidase (Cyd) and the cytoplasmic membrane-localized alternative respiratory t

181 c access without the toxicity of nonspecific cytoplasmic membrane lysis.

182 enerate holes in the cell wall through which cytoplasmic membrane material protrudes and is released

183 Through these openings, cytoplasmic membrane material protrudes into the extrace

184 regulate gene expression whereas Set-beta at cytoplasmic membranes may regulate unique cofactors, inc

185 teins, members of which reside in either the cytoplasmic membrane (NfsD, -E, and -G) or outer membran

186 hrinkage, resembling the constriction of the cytoplasmic membrane, occurs at ZipA densities higher th

187 Effector domains of MARTX toxins cross the cytoplasmic membrane of a host cell through a putative p

188 cantly stronger capacity to permeabilize the cytoplasmic membrane of Bacillus megaterium than theroma

189 hinery transports folded proteins across the cytoplasmic membrane of bacteria and the thylakoid membr

190 ates transport of folded proteins across the cytoplasmic membrane of bacteria and the thylakoid membr

191 tegration of most membrane proteins into the cytoplasmic membrane of bacteria occurs co-translational

192 osphatidylglycerol (PG) to form aa-PG in the cytoplasmic membrane of bacteria.

193 ation of a galactoside and a H(+) across the cytoplasmic membrane of Escherichia coli (galactoside/H(

194 Galactoside/H(+) symport across the cytoplasmic membrane of Escherichia coli is catalyzed by

195 proton-coupled zinc transporter found in the cytoplasmic membrane of Escherichia coli.

196 through a protein-conducting channel in the cytoplasmic membrane of eubacteria.

197 hat, after secretion, localizes to the inner cytoplasmic membrane of eukaryotic cells, where it exert

198 suggest that the compound cannot disrupt the cytoplasmic membrane of gram-negative bacteria because i

199 er anionic lipids in a mixture mimicking the cytoplasmic membrane of Gram-negative bacteria, as measu

200 vestigated the MBH protein purified from the cytoplasmic membrane of hoxR mutant cells.

201 his protein was found to be expressed on the cytoplasmic membrane of human monocytes.

202 or-3 protein localizes asymmetrically on the cytoplasmic membrane of neoblasts, and the ratio of asym

203 anslocating fully folded proteins across the cytoplasmic membrane of prokaryotes and the thylakoid me

204 stem translocates folded proteins across the cytoplasmic membrane of prokaryotes and the thylakoid me

205 Holins form pores in the cytoplasmic membranes of bacteria for the primary purpos

206 phosphate-linked oligosaccharides across the cytoplasmic membranes of bacteria.

207 obial peptides (AMPs) directly attacking the cytoplasmic membranes of Escherichia coli spheroplasts.

208 The drug interacts with the cytoplasmic membranes of Gram-positive pathogens, causin

209 ransport of fully folded proteins across the cytoplasmic membranes of many bacteria and the chloropla

210 rt of the molecular ion across the outer and cytoplasmic membranes of the Gram-negative bacteria is r

211 meshwork that is localized between adjacent cytoplasmic membranes of the myelin sheath.

212 nic pathway for protein secretion across the cytoplasmic membrane or insertion of integral membrane p

213 itive bacteria, CPS linkage is to either the cytoplasmic membrane or the cell wall.

214 targeting delivers proteins to the bacterial cytoplasmic membrane or to the eukaryotic endoplasmic re

215 he delivery of exogenous vectors through the cytoplasmic membrane, paving the way to the design of no

216 cells is by causing a profound defect in the cytoplasmic membrane permeability barrier.

217 icity in a psp null strain and the extent of cytoplasmic membrane permeability to large molecules.

218 of the third ejected protein, gp16, into the cytoplasmic membrane probably completes the overall tran

219 ta suppressed, whereas Set-beta localized to cytoplasmic membranes promoted neurite growth in rodent

220 In this study, we have discovered that the cytoplasmic membrane protease FtsH is involved in this p

221 TonB-dependent transducer (PSPTO_1206) and a cytoplasmic membrane protein (PSPTO_2145), which is loca

222 cterized were lambda Rz and Rz1, an integral cytoplasmic membrane protein and an outer membrane lipop

223 isulfide bonds into substrates, and then the cytoplasmic membrane protein DsbB reoxidizes DsbA's cyst

224 ognized by IcsA requires the activity of the cytoplasmic membrane protein insertase YidC.

225 Expression of the cytoplasmic membrane protein RipA is required for Franci

226 We show that as a cytoplasmic membrane protein, ASIC1 is also associated w

227 In Escherichia coli, cytoplasmic membrane proteins ExbB and ExbD couple the p

228 Current data suggest that cytoplasmic membrane proteins ExbB and ExbD harness pmf

229 Cytoplasmic membrane proteins ExbB and ExbD harness the

230 Cytoplasmic membrane proteins ExbB and ExbD of the Esche

231 In Escherichia coli, cytoplasmic membrane proteins ExbB and ExbD promote conf

232 The cytoplasmic membrane proteins harvest and transmit the p

233 proteins B (PspB) and C (PspC) are integral cytoplasmic membrane proteins involved in inducing the Y

234 Here, we show that YciB and DcrB, two small cytoplasmic membrane proteins of previously unknown func

235 The cytoplasmic membrane proteins PspB and PspC are critical

236 In contrast, PspA associates with the cytoplasmic membrane proteins PspBC during inducing cond

237 PspB and PspC are cytoplasmic membrane proteins required for stress-depend

238 Escherichia coli TonB system consists of the cytoplasmic membrane proteins TonB, ExbB, and ExbD and m

239 The TonB system couples cytoplasmic membrane proton motive force (pmf) to active

240 The TonB system couples cytoplasmic membrane proton motive force to TonB-gated o

241 e transporters using energy derived from the cytoplasmic membrane proton motive force.

242 In gram-negative bacteria, the cytoplasmic membrane proton-motive force energizes the a

243 D of the Escherichia coli TonB system couple cytoplasmic membrane protonmotive force (pmf) to TonB.

244 e point mutation, E613R, introduced into the cytoplasmic membrane-proximal "wedge" domain of CD45 is

245 aking unmediated diffusion of NH3 across the cytoplasmic membrane rate-limiting for cell growth in a

246 , at least in part through the disruption of cytoplasmic membrane related functions, and that resista

247 h SecA2 drives export of proteins across the cytoplasmic membrane remains poorly understood.

248 ane, hydrophilic outer membrane, and outer + cytoplasmic membrane, respectively.

249 integral membrane proteins of the bacterial cytoplasmic membrane responsible for biosynthesis of pep

250 -transducing protein that is anchored in the cytoplasmic membrane, resulted in a fivefold larger valu

251 , predicted to export the protein beyond the cytoplasmic membrane, resulted in loss of functional tra

252 ith molecules of the cell wall and perforate cytoplasmic membranes resulting in bacterial cell death.

253 ddenly trigger to cause lethal damage to the cytoplasmic membrane, resulting in the cessation of resp

254 s stockpile nuclear pore complexes (NPCs) in cytoplasmic membrane sheets called annulate lamellae (AL

255 led cytochrome bd 1 ubiquinol oxidase in the cytoplasmic membrane show that CpcA-PEB and CpcA-PCB are

256 pesvirus-4 perturbs B cell signaling using a cytoplasmic/membrane shuttling factor that nucleates the

257 tion by the terminal oxidases located at the cytoplasmic membrane significantly affects the activitie

258 s to an inability of cells to trim tubulated cytoplasmic membranes, some of which extend from lipopha

259 gression by guiding the targeted delivery of cytoplasmic membrane stores to the cell surface through

260 ely with no contamination from lipids of the cytoplasmic membrane, such as phosphatidylglycerol.

261 (betagamma) binds, becomes accessible to the cytoplasmic membrane surface where G(betagamma) resides.

262 transmembrane segment 2 (TM2) and TM3 on the cytoplasmic membrane surface.

263 aeroides is initiated at indentations of the cytoplasmic membrane, termed UPB.

264 exes are organized in extended arrays in the cytoplasmic membrane that allow bacteria to respond to c

265 are unclear, as these cells possess a single cytoplasmic membrane that is surrounded by a thick cell

266 al cell wall, forming a meshwork outside the cytoplasmic membrane that maintains cell shape and preve

267 the formation of a signaling complex at the cytoplasmic membrane that responds to environmental Pi l

268 e RNA virus is the modification of host cell cytoplasmic membranes that serve as sites of viral RNA s

269 ion and folding of proteins in the bacterial cytoplasmic membrane, the chloroplast thylakoid membrane

270 Seconds after LL-37 penetrates the cytoplasmic membrane, the chromosomal DNA becomes rigidi

271 In the cytoplasmic membrane, the Hup transporter was specific f

272 serine, an acidic lipid prevalent in various cytoplasmic membranes, thereby enhancing the lipid speci

273 d by the association of FtsZ polymers to the cytoplasmic membrane through the membrane-tethering FtsA

274 y inevitably trigger water fluxes across the cytoplasmic membrane, thus impinging on the degree of ce

275 ssential for maintaining self-renewal on the cytoplasmic membrane to cope with low ligand levels outs

276 ia uses the proton motive force (PMF) of the cytoplasmic membrane to energize active transport of nut

277 ems transduce the proton motive force of the cytoplasmic membrane to energize substrate transport thr

278 stator units that couple ion flow across the cytoplasmic membrane to generate torque.

279 owth halts does the peptide permeabilize the cytoplasmic membrane to GFP and the small dye Sytox Gree

280 er translocates virulence factors across the cytoplasmic membrane to the cell wall, cell surface, and

281 ples the translocation of protons across the cytoplasmic membrane to the synthesis or hydrolysis of A

282 a previously uncharacterized iron-repressed cytoplasmic membrane transporter system, fbpABC, that is

283 anonical holins accumulate harmlessly in the cytoplasmic membrane until they suddenly trigger to form

284 d by detergent treatment to permeabilize the cytoplasmic membrane, up to 15-fold enhancement in the r

285 ese robust reconstituted proteoliposomes and cytoplasmic membrane vesicles have revealed that the num

286 when assessed in their native environment of cytoplasmic membrane vesicles.

287 otein that is attached to the outside of the cytoplasmic membrane via a covalent diacylglycerol ancho

288 Association of PflB with the cytoplasmic membrane was shown to be FocA dependent and

289 ison, vesicles representing all parts of the cytoplasmic membrane were captured by expressing a Tar v

290 tions of the outer permeability barriers and cytoplasmic membranes were found to be dependent on grow

291 No defects in the transport of capsids to cytoplasmic membranes were observed, but the wrapping of

292 the proper integration of the enzyme at the cytoplasmic membrane, which is mediated by the extended

293 roteins form a macromolecular complex at the cytoplasmic membrane, which we have purified and charact

294 microscopy shows that FtsH1 is mainly in the cytoplasmic membrane, while the remaining FtsH proteins

295 Most bacteria surround their cytoplasmic membrane with a net-like, elastic heteropoly

296 Bacteria surround their cytoplasmic membrane with an essential, stress-bearing p

297 d with a signal peptide securing them to the cytoplasmic membrane with the lipoprotein domain in the

298 d that RipA has a unique topology within the cytoplasmic membrane, with the N and C termini in the cy

299 Sec pathway to transport proteins across the cytoplasmic membrane, with the SecA ATPase playing a cen

300 The resultant bacterial ghosts contain cytoplasmic membrane within bacteria-shaped peptidoglyca