ライフサイエンスコーパス: sulfhydryl

1 e that specifically labels reactive cysteine sulfhydryls.

2 ally deglutathionylate cysteines and restore sulfhydryls.

3 1.Tb, possessing a maleimide moiety, as its sulfhydryl acceptor, was poorly emitting in aqueous pH 7

4 ify proximal relationships of the introduced sulfhydryls across the proposed interdomain interface.

5 ective capture method promoted enrichment of sulfhydryl analytes and reduced matrix interferences, th

6 ed mesh substrates were then used to capture sulfhydryl analytes directly from urine and plasma sampl

7 d 60 umol/g MP) under GOx treatment promoted sulfhydryl and amine loss (up to 58% and 49%, respective

8 containing structural motifs such as selenyl-sulfhydryl and diselenide bonds.

9 irming the critical requirement of both free sulfhydryl and galactosamine moieties for inhibition of

10 l mice, with greater depletion of nonprotein sulfhydryl and occurrence of cytotoxicity (observable by

11 wo coordination sites filled by the cysteine sulfhydryls, and another by the amide nitrogen of Phe (3

12 ical activities of 6-DHSG were attenuated by sulfhydryl antioxidants such as glutathione (GSH) or N-a

13 confocal microscopy, extractability and free sulfhydryl assays.

14 eveloped to determine the percentage of free sulfhydryl at each cysteine residue of four recombinant

15 s glucose to the growth medium (termed 'High Sulfhydryl Bacillus subtilis' or HSBS) was compared to t

16 ncentration of sulfhydryl sites (termed 'Low Sulfhydryl Bacillus subtilis' or LSBS) and to sorption o

17 These data support the evaluation of sulfhydryl-based Id-KLH vaccines in lymphoma clinical tr

18 A sulfhydryl-based tumor Ag-carrier protein conjugation sy

19 could be abolished by the membrane-permeable sulfhydryl blocker, N-ethylmaleimide, by the RGD peptide

20 However, in this case a sulfhydryl bond is cleaved to release the lipophilic cyt

21 es surfaces through the formation of Ag(+I)--sulfhydryl bonds.

22 istances of 2.24-2.34 A were consistent with sulfhydryl-bound As(III).

23 sulfhydryl detection revealed the rupture of sulfhydryl bridges.

24 al redox-sensing properties through reactive sulfhydryl chemistry.

25 e methylene group with a nitrogenous base or sulfhydryl compound.

26 sediment were present as Ag(2)S (55%) and Ag-sulfhydryl compounds (27%).

27 such as aniline and veratrylamine as well as sulfhydryl compounds such as l-cysteine and beta-mercapt

28 al from Pseudomonas putida, and the measured sulfhydryl concentrations on bacterial EPS molecules are

29 This study suggests that the sulfhydryl concentrations on EPS molecules may vary sign

30 Sulfhydryl-containing compounds, including thiols and hy

31 effectively separate the reactivity of these sulfhydryl-containing compounds.

32 highlight the importance of modifications by sulfhydryl-containing ligands that can drastically influ

33 rapid response (<1 min) and is selective for sulfhydryl-containing nucleophiles over other reactive s

34 processing characterized by the loss of free sulfhydryl content (Fas-SH) and resultant increases in S

35 The presence of salt decreased the free sulfhydryl content but increased the beta-sheet structur

36 ment decreased the alpha-helix content, free sulfhydryl content, and Rg, it increased the random coil

37 Salt-soluble protein, surface reactive sulfhydryl content, and surface hydrophobicity of Alaska

38 ance, particle size, protein fractions, free sulfhydryl content, immunoreactivity, viscosity, gelling

39 ance, particle size and microstructure, free sulfhydryl content, protein fractions, protein electroph

40 rease in surface hydrophobicity and reactive sulfhydryl content; structurally, no clear denaturation

41 dies showed that the gamma subunit disulfide/sulfhydryl couple in the modified ATP synthase has a mor

42 ectrospray ionization-MS/MS as follows: 1) a sulfhydryl cross-link between C3.53(134) in TMH3 and the

43 using nonreduced polyacrylamide gels and the sulfhydryl cross-linker BMH.

44 Mia40 and the sulfhydryl:cytochrome c oxidoreductase Erv1/ALR are esse

45 aIIbbeta3 and alphavbeta3 and suggest a free sulfhydryl-dependent regulatory role for Cys-560-Cys-583

46 quantum efficiencies (Q(u)) of the amino and sulfhydryl derivatives were about an order of magnitude

47 The free sulfhydryl detection revealed the rupture of sulfhydryl

48 tructural changes, arising from disulfide or sulfhydryl-disulfide bond-mediated aggregation of whey p

49 tributed to the significant reduction in the sulfhydryl-disulfide interchange reaction during denatur

50 with dithiothreitol indicated occurrence of sulfhydryl-disulfide interchange reactions.

51 Given our previous identification of sulfhydryl/disulfide redox status as a factor in photore

52 rent antibodies had different levels of free sulfhydryl due to multiple unpaired cysteine residues co

53 Furthermore, free sulfhydryl due to unpaired cysteine residues in the vari

54 chemical modification and inhibition of the sulfhydryl enzyme, glyceraldehyde-3-phosphate dehydrogen

55 cycle resulted in the catalytic oxidation of sulfhydryls even with nanomolar concentrations of seleni

56 s as well as gluten proteins; it removes the sulfhydryl group and leads to the formation of disulfide

57 jor site of HSA adduction is the single free sulfhydryl group at Cys34, we used thiol-affinity resins

58 of single stranded DNA (ssDNA) probe through sulfhydryl group at the 5' phosphate end.

59 ealed that this mutation made the regulatory sulfhydryl group energetically much more difficult to re

60 tain a more stable form for oral dosing, the sulfhydryl group in conjugate 1 was converted into a fun

61 nges, specific for thiamine and sensitive to sulfhydryl group inhibition.

62 ine-persulfide (Cys-SSH) is a cysteine whose sulfhydryl group is covalently bound to sulfur (sulfane

63 yltriglycine with S-acetyl protection of the sulfhydryl group may be used to conjugate MAG3 to primar

64 Besides the sulfhydryl group of a cysteine, we make use of an azido

65 minal carbon of the acetylene moiety and the sulfhydryl group of Cys-803 at the solvent interface.

66 The reactive sulfhydryl group of Cys106 projects toward position C-4a

67 e presence of monovalent copper ions and the sulfhydryl group of Cys466.

68 olution containing NEM which reacts with the sulfhydryl group of GSH, thus locking the active form in

69 ilic attack of either the amine group or the sulfhydryl group of the substrate on the internal aldimi

70 ue containing a methyl group in place of the sulfhydryl group present in Cys, for the native Cys resi

71 t protein damage, characterised by the total sulfhydryl group reduction.

72 pproach, a cemadotin derivative containing a sulfhydryl group results in a mixed disulfide linkage.

73 enzymes that generate a product with a free sulfhydryl group, including histone acetyltransferases,

74 cysteine, which adds to the cofactor via its sulfhydryl group, possibly forming a cyclic thiazolidine

75 ain why cysteine, despite possessing a polar sulfhydryl group, tends to behave as a hydrophobic (rath

76 ng advantage of the reactivity of cysteine's sulfhydryl group, we modified these mutants with chemica

77 ddition or subtraction of a hydrogen atom or sulfhydryl group.

78 nt of an NO moiety to a nucleophilic protein sulfhydryl group.

79 al cross linking to a gold surface through a sulfhydryl group.

80 -isoascorbic acid (DIA), on the oxidation of sulfhydryl groups (-SH) to disulfide bonds (-SS-) of ext

81 e protein, thioredoxin, between two cysteine sulfhydryl groups (i.e., staple), followed by photochemi

82 Binding of arsenite (As(III)) to sulfhydryl groups (Sorg(-II)) plays a key role in As det

83 res higher than 200 MPa, a decrease in total sulfhydryl groups and an increase in surface hydrophobic

84 ary lipid oxidation products and the loss in sulfhydryl groups and Ca(2+)-ATPase activity.

85 ified the GR protein by decreasing available sulfhydryl groups and decreasing nuclear GR expression a

86 It triggers a rapid covalent destruction of sulfhydryl groups and disulfide bonds via the mechanism

87 esults, obtained from the reactivity of free sulfhydryl groups and fluorescence analysis, showed that

88 tein carbonyl content, oxidised amino acids, sulfhydryl groups and immuno-blotting against carbonyl g

89 The level of accessible free sulfhydryl groups and the surface hydrophobicity of unfo

90 arsenite; and d) As has a high affinity for sulfhydryl groups and therefore binds to GSH and Cys.

91 The sulfhydryl groups at the end of the molecular wire form

92 ns that favored closure, indicating that the sulfhydryl groups come close enough to each other or to

93 nd B2 remained unchanged, while free exposed sulfhydryl groups decreased.

94 The presence of free sulfhydryl groups in five recombinant monoclonal antibod

95 duction-oxidation modifications of cysteinyl sulfhydryl groups in mature ADAM17 may serve as a mechan

96 can be used to quantify reactions targeting sulfhydryl groups in proteins.

97 The amount of titrated sulfhydryl groups in the protein concentration range inv

98 the reductase activity is unique in that no sulfhydryl groups in the YfcG protein are covalently inv

99 theless, no derivatization strategy for free sulfhydryl groups in tissue is known for MALDI MSI.

100 sted that the presence of low levels of free sulfhydryl groups is likely a common feature of recombin

101 s a T-rich probe DNA at one vertex and three sulfhydryl groups modified with 10nm Au NPs at the other

102 Arsenic binding by sulfhydryl groups of natural organic matter (NOM) was re

103 ecently, the complexation of trivalent As by sulfhydryl groups of NOM was proposed as the main mechan

104 e the formation of adducts with nucleophilic sulfhydryl groups on cysteine residues of selected prote

105 hat these methods had a high selectivity for sulfhydryl groups on this protein, which accounted for t

106 on in vitro and decreased the number of free sulfhydryl groups on tubulin cysteines.

107 in gold or self-assembled monolayer via the sulfhydryl groups present in the hinge region.

108 n of complexes involving mercury species and sulfhydryl groups present in tissues and/or loss of wate

109 Reversibly oxidized cysteine sulfhydryl groups serve as redox sensors or targets of r

110 t as antioxidant drugs directly through free sulfhydryl groups that serve as a source of reducing equ

111 oyl cofactor, which is the attachment of two sulfhydryl groups to C6 and C8 of a pendant octanoyl cha

112 nd the use of a molecular wire terminated in sulfhydryl groups to connect the two modules.

113 the selective oxidation of protein cysteine sulfhydryl groups to disulfide bonds we examined the spe

114 capacity against peroxyl radicals, DPPH, and sulfhydryl groups were analyzed.

115 The locations of the free sulfhydryl groups were determined using mass spectrometr

116 plasmin activity, prolidase level, and total sulfhydryl groups were evaluated.

117 Free sulfhydryl groups were first modified using 5-idoacetami

118 Redox-dependent modifications of sulfhydryl groups within the two Cys4 zinc fingers of th

119 ), has no other active redox moieties (e.g., sulfhydryl groups) and can exist in three different oxid

120 and Msh2-Msh6 interactions involve cysteine sulfhydryl groups, and the high Cd(2+):Msh2-Msh6 ratio i

121 Zeta potential, disulfide-sulfhydryl groups, surface hydrophobicity, secondary str

122 of Ag(+) and/or Cd(+2) with the substituted sulfhydryl groups.

123 ated As was present as trivalent As bound by sulfhydryl groups.

124 x1, which was mainly fully reduced with five sulfhydryl groups.

125 fluorescence detection of peptides with free sulfhydryl groups.

126 proteins and other ligands to silica through sulfhydryl groups.

127 isulfide bridges with cysteine or methionine sulfhydryl groups.

128 the dynamic chemistry played by wine protein sulfhydryl groups.

129 sured were the levels of prolidase and total sulfhydryl groups.

130 Disruption of sulfhydryl homeostasis, which resulted in ER stress, acc

131 DOPA) which is a pro-oxidant and may disrupt sulfhydryl homeostasis.

132 proteins tend to have higher proportions of sulfhydryl, hydroxyl and acylamino, but lower of sulfide

133 ree sulfhydryl, similar distribution of free sulfhydryl in the domain structures was observed in the

134 of p65-NFkappaB to DNA, suggesting that most sulfhydryls in p65-NFkappaB protein were in reduced and

135 dely used reagent for the alkylation of free sulfhydryls in proteomic experiments.

136 ugh a redox modification of vicinal cysteine sulfhydryls in the catalytic domain of PKC.

137 onality with biological nucleophilic groups (sulfhydryl, indole, phenol, imidazole, carboxamide) that

138 Oxidation of crystallin methionine and sulfhydryls into sulfoxides was dramatically increased,

139 te covalently modifies beta2M286C side-chain sulfhydryls, irreversibly altering GABA-induced currents

140 A low percentage of free sulfhydryl is a common feature of recombinant monoclonal

141 ombination of LacZ/PhoA reporter fusions and sulfhydryl labelling by PEGylation of novel cysteine res

142 oteins, resulting in overall decreased total sulfhydryl levels.

143 Our results thus document that sulfhydryl ligands are highly competitive As(III) comple

144 The ability of sulfhydryl ligands to compete with ferrihydrite for As(I

145 polyethylene glycol-2000], are conjugated to sulfhydryl lipids via maleimide reactive groups on the Q

146 gation between the cross-linked peptides and sulfhydryl magnetic beads by analyzing supernatant solut

147 confirming that peptides can be isolated on sulfhydryl magnetic beads by using Sulfo-LC-SPDP.

148 ormation of Sorg(-II)-As(III) complexes on a sulfhydryl model adsorbent (Ambersep GT74 resin) in the

149 We also measured rates of sulfhydryl modification by p-chloromercuribenzenesulfona

150 GABA altered the rates of sulfhydryl modification of alpha1K219C, beta2K213C, and

151 This was substantiated by site-directed sulfhydryl modification of the proton glutamate mutant E

152 Sulfhydryl modification of Y124C by 2-aminoethyl methane

153 ccess to the nano-pockets by mutagenesis and sulfhydryl modification, and monitor channel conformatio

154 ed to wild-type levels upon reduction of the sulfhydryl modification.

155 Here, we examined sulfhydryl modifications of the p65 subunit of NFkappaB

156 arrying out selective desulfurization of the sulfhydryl-modified sugar moiety in the presence of acet

157 l methanethiosulfonate (a membrane-permeable sulfhydryl modifier)-mediated enhancement of the binding

158 ctivity was sensitive to N-ethylmaleimide, a sulfhydryl-modifying reagent.

159 probed with a series of methanethiosulfonate sulfhydryl-modifying reagents.

160 kedly enhanced the accessibility of cysteine sulfhydryl moieties in DAT as probed by a membrane-imper

161 hydroxyl group or conversion of a methyl or sulfhydryl moiety to a hydroxyl, can confer modified Ag-

162 n are two highly conserved, vicinal cysteine sulfhydryl motifs (cysteine-X-X-cysteine), which are wel

163 tissue antioxidants [estimated by nonprotein sulfhydryl (NPSH) levels] and/or induction of oxidant st

164 The incorporation of a sulfhydryl nucleophile into a phosphoinositide hapten de

165 n between isothiocyanate of sulforaphane and sulfhydryl nucleophiles of Keap1 is kinetically labile,

166 tates catalysis by hydrogen bonding with the sulfhydryl of Cys-aldimine.

167 re/function and/or prevents degradation from sulfhydryl overoxidation or proteolysis.

168 es the substrate specificity of the quiescin sulfhydryl oxidase (QSOX) family of disulfide-generating

169 The quiescin sulfhydryl oxidase (QSOX) family of enzymes generates di

170 ge) showed it to be a member of the Quiescin-sulfhydryl oxidase (QSOX) family.

171 Quiescin sulfhydryl oxidase (QSOX) flavoenzymes catalyze the dire

172 The flavin-dependent quiescin-sulfhydryl oxidase (QSOX) inserts disulfide bridges into

173 The flavoprotein quiescin-sulfhydryl oxidase (QSOX) rapidly inserts disulfide bond

174 tein containing the ERV/ALR domain, quiescin-sulfhydryl oxidase (QSOX).

175 , PRDX4, and the candidate oxidants quiescin-sulfhydryl oxidase 1 (QSOX1) and vitamin K epoxide reduc

176 sion (SAGE) databases was enzyme quiescin Q6 sulfhydryl oxidase 1 (QSOX1).

177 ing that the C-X-X-C motif was essential for sulfhydryl oxidase activity and responsible for the alte

178 92 C(155)XXC(158) amino acids, important for sulfhydryl oxidase activity, were mutated to A(155)XXA(1

179 luble 62 kDa FAD-linked and EDTA-insensitive sulfhydryl oxidase apparently constitutes the dominant d

180 ysteine and selenomethionine residues in the sulfhydryl oxidase augmenter of liver regeneration (ALR)

181 and depend on the oxidoreductase Mia40, the sulfhydryl oxidase augmenter of liver regeneration (ALR)

182 The sulfhydryl oxidase augmenter of liver regeneration (ALR)

183 Reoxidation of Mia40 is facilitated by the sulfhydryl oxidase Erv1 and the respiratory chain.

184 The sulfhydryl oxidase Erv1 partners with the oxidoreductase

185 ctions involving disulfide transfer from the sulfhydryl oxidase Erv1 to Mia40 and from Mia40 to subst

186 us pathway with the oxidoreductase Mia40 and sulfhydryl oxidase Erv1, termed the mitochondrial interm

187 hen in excess or at a lower rate by only the sulfhydryl oxidase Erv1.

188 t that Tim17 can be directly oxidized by the sulfhydryl oxidase Erv1.

189 Erv1 is a flavin-dependent sulfhydryl oxidase in the mitochondrial intermembrane sp

190 with the augmenter of liver regeneration, a sulfhydryl oxidase of the mitochondrial intermembrane sp

191 ously linked to cancer, most strongly on the sulfhydryl oxidase Qsox1 which we show is required for m

192 neration (ALR) is both a growth factor and a sulfhydryl oxidase that binds FAD in an unusual helix-ri

193 1-like (Gfer) is an evolutionarily conserved sulfhydryl oxidase that is enriched in embryonic and adu

194 The first mammalian sulfhydryl oxidase to be described was an iron-dependent

195 family of flavin adenine dinucleotide-linked sulfhydryl oxidases and is related to the ERV/ALR family

196 Both metal and flavin-dependent sulfhydryl oxidases catalyze the net generation of disul

197 These metazoan sulfhydryl oxidases have four recognizable domains: a re

198 AD prosthetic group of the ERV/ALR family of sulfhydryl oxidases is housed at the mouth of a 4-helix

199 ies between members of the ERV/ALR family of sulfhydryl oxidases provides insights into their likely

200 ases and is related to the ERV/ALR family of sulfhydryl oxidases.

201 on to the earlier reports of metal-dependent sulfhydryl oxidases.

202 redox capacity and reduces cellular protein sulfhydryl oxidation and, in particular, oxidation of mi

203 To gain insight into the requirement for sulfhydryl oxidation during virus replication, a virus w

204 t increased Prx expression and resistance to sulfhydryl oxidation in Abeta-resistant nerve cells is a

205 Conversely, increased intracellular heme or sulfhydryl oxidation inactivate BACH1, permitting transc

206 The documentation of a sulfhydryl-oxidizing activity in the thylakoid lumen fur

207 M), a pharmacologically active member of the sulfhydryl proteolytic enzyme family, obtained from Anan

208 containing alpha-beta unsaturated carbonyls, sulfhydryl reactive metals, and isothiocyanates are stro

209 beta unsaturated carbonyls, isothiocyanates, sulfhydryl reactive metals, flavones, and polyphenols.

210 The sulfhydryl reactive reagent 2-(trimethylammonium)ethyl m

211 Intracellular application of the sulfhydryl reactive reagent MTSET using CLH-3b channels

212 a7 ligand-binding domain allowing us to bind sulfhydryl-reactive (SH) agonist analogs or control reag

213 in CHO cells and covalently labeled with the sulfhydryl-reactive fluorophore monobromo-trimethylammon

214 method, which utilizes cysteine residues and sulfhydryl-reactive nitroxide reagents, can be challengi

215 The sulfhydryl-reactive oxidative agent diamide suppressed L

216 s-linking screen using the photoactivatable, sulfhydryl-reactive reagent N-[4-(p-azidosalicylamido)bu

217 modification of the introduced cysteines by sulfhydryl-reactive reagents in the absence and presence

218 issue by utilizing our previously developed sulfhydryl-reactive, cleavable, radioiodinated photocros

219 eptors expressed in Xenopus oocytes with the sulfhydryl-reactive, environmentally sensitive fluoresce

220 d their accessibility to modification by the sulfhydryl reagent 3-(N-maleimido-propionyl) biocytin (M

221 hione (GSH) involves oxidation of GSH by the sulfhydryl reagent 5,5'-dithio-bis(2-nitrobenzoic acid)

222 essibility of introduced Cys residues to the sulfhydryl reagent MTSET.

223 es for alpha7-W55C nAChRs, whereas a neutral sulfhydryl reagent potentiated responses; residue C55 wa

224 -less CLH-3b mutant, we demonstrate that the sulfhydryl reagent reactivity of substituted cysteines a

225 harge restoration using a negatively charged sulfhydryl reagent reinstated also the WT phenotype.

226 Exposure to oxidative stress via the sulfhydryl reagent thimerosal resulted in a greater decr

227 bition of transport by a membrane impermeant sulfhydryl reagent was diminished under conditions expec

228 endogenous cysteine to a membrane impermeant sulfhydryl reagent was enhanced by the D451E mutation, s

229 us cysteine residue to a membrane-impermeant sulfhydryl reagent was increased relative to wild type,

230 vity of the mutants to a membrane-impermeant sulfhydryl reagent was not conformationally sensitive.

231 n externally applied and membrane-impermeant sulfhydryl reagent.

232 by p-chloromercuriphenylsulfonate (pCMPS), a sulfhydryl reagent.

233 Cytoplasmically applied membrane-impermeant sulfhydryl reagents alter the Ca2+ sensitivity of Ano1 E

234 te their sensitivity to membrane-impermeable sulfhydryl reagents as exchanger current block.

235 Several positively charged sulfhydryl reagents blocked ACh-induced responses for al

236 ed to the loss of the ability of the charged sulfhydryl reagents to inhibit NBMPR binding in isolated

237 However, the capacity of charged sulfhydryl reagents to inhibit the binding of NBMPR in b

238 ha7-W55C) and testing the ability of various sulfhydryl reagents to react with this cysteine.

239 th membrane-permeant and membrane-impermeant sulfhydryl reagents under a variety of conditions.

240 mino)ethyl methanethiosulfonate (MTS-TAMRA)) sulfhydryl reagents, 4 with only BM, and 3 with only MTS

241 de of TM3, was affected by membrane-permeant sulfhydryl reagents.

242 robed their state-dependent accessibility to sulfhydryl reagents.

243 Thus, sulfhydryl redox modification can regulate various aspec

244 This enhancement was blocked by sulfhydryl reducing agents, demonstrating a reversible m

245 le manner, by treatment of the channels with sulfhydryl reducing agents, suggesting that it was mostl

246 In contrast, sulfhydryl reduction had limited effects on channel open

247 r that can be reversibly coupled to a target sulfhydryl residue via a disulfide bond.

248 Free sulfhydryl, resulting from the reduction of disulfide bo

249 othelial surfaces, NO is associated with the sulfhydryl-rich protein tissue transglutaminase (TG2), t

250 Nearly all the hits from our recent sulfhydryl-scavenging high-throughput screen (HTS) targe

251 e predicted based on the measurement of free sulfhydryl (-SH) content on applying mildly denaturing c

252 are involved in disulfide bonds, and no free sulfhydryl should be detected.

253 eagent, suggesting that interactions between sulfhydryl side chains of IDH2 Cys-150 residues limit ac

254 fferent locations in FepA and modified their sulfhydryl side chains with fluorescein maleimide in liv

255 ntibodies contained different levels of free sulfhydryl, similar distribution of free sulfhydryl in t

256 ose concentrations yielding higher bacterial sulfhydryl site concentrations for each species studied.

257 concentration does not significantly affect sulfhydryl site concentrations for S. oneidensis and P.

258 o the TSB medium significantly increases the sulfhydryl site concentrations for the three Bacillus sp

259 Our results suggest that bacterial sulfhydryl site concentrations in natural systems are li

260 ium enriched with 50 g/L of glucose, and the sulfhydryl site concentrations of the obtained biomass s

261 ss samples were determined through selective sulfhydryl site-blocking, potentiometric titrations, and

262 subtilis biomass with a low concentration of sulfhydryl sites (termed 'Low Sulfhydryl Bacillus subtil

263 emoval, indicating that virtually all of the sulfhydryl sites are located on the EPS molecules produc

264 Bacterial sulfhydryl sites can form strong complexes with chalcoph

265 These results suggest that bacterial sulfhydryl sites control the sorption behavior of these

266 ed in order to determine the distribution of sulfhydryl sites on bacteria.

267 In this study, the concentration of sulfhydryl sites on bacterial biomass samples with and w

268 is crucial to quantify the concentration of sulfhydryl sites on EPS molecules of other bacterial spe

269 mainly due to the elevated concentration of sulfhydryl sites on the bacteria.

270 biomass with induced high concentrations of sulfhydryl sites represents a promising and low cost bio

271 PS produced by S. oneidensis contained fewer sulfhydryl sites than those present on the untreated cel

272 media strongly affects the concentration of sulfhydryl sites that are present on the bacteria, with

273 After blocking the bacterial cell envelope sulfhydryl sites using a qBBr treatment, the sorption of

274 ida samples was 34.9 +/- 9.5 mumol/g, and no sulfhydryl sites were detected after EPS removal, indica

275 Prior to EPS removal, the measured sulfhydryl sites within P. putida samples was 34.9 +/- 9

276 In contrast, the sulfhydryl sites within the S. oneidensis samples increa

277 is biomass with an elevated concentration of sulfhydryl sites, induced by adding excess glucose to th

278 Furthermore, rapidly reacting, sulfhydryl-specific chemical cross-linkers, methanethios

279 Here, sulfhydryl-specific cross-linking strategy was employed

280 ution, allowing filaments to be labeled with sulfhydryl-specific fluorescent dyes.

281 ility studies using the membrane-impermeant, sulfhydryl-specific methanethiosulfonate reagents.

282 f SNAP on N-type currents was blocked by the sulfhydryl-specific modifying reagent methanethiosulfona

283 of oocytes in the presence of the impermeant sulfhydryl-specific reagent, p-chloromercuribenzene sulf

284 bility method using the membrane-impermeant, sulfhydryl-specific reagent, p-chloromercuribenzene-sulf

285 ulfide linkage with the active site cysteine sulfhydryl specifically.

286 Surface reactive sulfhydryl (SRSH) contents of the three fish species beh

287 Iron affects the sulfhydryl status of Yap5, which is indicative of the ge

288 Surface hydrophobicity, sulfhydryl status, secondary structure profile, differen

289 ring-opened AP site and the alpha-amino and sulfhydryl substituents of its amino-terminal cysteine r

290 avenger capacity) and cellular antioxidants (sulfhydryl, superoxide dismutase) of zebrafish brain wer

291 Protein sulfhydryls that had undergone H2O2 mediated glutathiony

292 e concentrations of GSH and other nonprotein sulfhydryls through binding and irreversible loss in bil

293 information correlating the presence of free sulfhydryl to specific cysteine residues.

294 roxy for dimethylamino (DMAQ and DMAQ-Cl) or sulfhydryl (TQ) significantly alters the photochemical a

295 tion of isolates among cefotaximase (CTX-M), sulfhydryl variable, and temoneira enzymes and data on p

296 A low percentage of free sulfhydryl was detected at every cysteine residue in the

297 Free sulfhydryl was first alkylated with 12C iodoacetic acid.

298 Interestingly, free sulfhydryl was rarely associated with cysteine residues

299 The percentage of free sulfhydryl was then calculated using the two m/z series

300 Cysteine sulfhydryls within CCTalpha are needed for full catalyti