ライフサイエンスコーパス: thiol group

1 ontained an N(2)-modified dG with a reactive thiol group).

2 ially react with the disulfide bond, but not thiol group.

3 on of a tight-binding inhibitor possessing a thiol group.

4 ine residue of caspase-3 and also contains a thiol group.

5 related with changes in accessibility of the thiol group.

6 the N-terminal methionine, generates a free thiol group.

7 binding cleft approximately 6 A from the GSH thiol group.

8 d reduced by phosphorylation of the cysteine thiol group.

9 ing domain of aggregin contains an essential thiol group.

10 he surface of SERS-active substrates via the thiol group.

11 catalytic zinc into position to activate the thiol group.

12 group of HMBPP is replaced by an amino and a thiol group.

13 teamine to afford a monolith rich in surface thiol groups.

14 teamine to afford a monolith rich in surface thiol groups.

15 ld nanoparticles attached to DNA ligands via thiol groups.

16 ond cleavage with charge retention at the C1 thiol groups.

17 of control of the spatial arrangement of the thiol groups.

18 e stoichiometric with that of the introduced thiol groups.

19 ubmodel, were combined with strongly binding thiol groups.

20 change of both backbone amide and side-chain thiol groups.

21 their disulfide bonds in concert with their thiol groups.

22 and group-specific reagents directed toward thiol groups.

23 ecting group was used to avoid handling free thiol groups.

24 ntial nitrosylation of up to 20 thus-exposed thiol groups.

25 hat deacylation concomitantly generates free thiol groups.

26 n surface hydrophobicity and exposure of the thiol groups.

27 n of total intracellular Pb was complexed by thiol groups.

28 ing accessibility and full reactivity of the thiol groups.

29 n acrylamide derivative which can react with thiol groups.

30 he complexation of the intracellular As with thiol groups.

31 d transfer of a nitric oxide (NO) group to a thiol group].

32 nT, all known vertebrate TnT isoforms lack a thiol group, a property which makes the wild-type protei

33 However, the thiol groups anchoring the polymeric envelope to the ZnS

34 coiled ssDNA molecules each anchored via the thiol group and at possibly one or two other bases.

35 tive to the pKa of the attacking active site thiol group and changes with the structure of the leavin

36 due to an oxidative attack of the pro-domain thiol group and disruption of its inhibitory coordinatio

37 roduct binds to the zinc active site via the thiol group and is therefore the active CA inhibitor, wh

38 on the number of methylene units between the thiol group and pentanedioic acid.

39 that utilizes a cross-linker with a cryptic thiol group and using beads modified with a photocleavab

40 fied by 3-glycidopropyltrimethoxysilane with thiol groups and 5nm gold nanoparticles (GNPs) was estab

41 ups, 12 amidino groups, 6 thiol groups, or 6 thiol groups and 6 carboxylic acid groups in protected f

42 A) derivatives bearing linkers with terminal thiol groups and a preliminary evaluation of their poten

43 d age-related accrual of oxidation damage to thiol groups and age-associated up-regulation of homeost

44 been shown to harbour functionally important thiol groups and are encoded by genes that are considere

45 is the relative accessibility of both their thiol groups and disulfide bonds.

46 light and heavy chains that provide reactive thiol groups and do not perturb immunoglobulin folding a

47 nked with deprotonation of the co-ordinating thiol groups and folding of the polypeptide.

48 Importantly, the synthesis is free of thiol groups and halide ions, thus providing a possible

49 ing capacity, protein-bound carbonyl groups, thiol groups and metal chelation activities in addition

50 The CBD(CelK) has three thiol groups and one disulfide, reduction of which resul

51 oung MRs have 1.6 times as much free protein thiol groups and similar amounts of reversible oxidative

52 to their potential for the quantification of thiol groups and thiol ligands on different types of nan

53 residues, acetylation, and nitrosylation of thiol groups and tyrosine residues, have received compar

54 y are less susceptible to oxidation than the thiol groups and, thus, afford no protection against cys

55 de and 4,4'-dipyridyl disulfide (titrants of thiol groups), and two closely related Michael reaction

56 ed into other groups such as a carboxylic or thiol group, and the DPA analog can be covalently attach

57 ilization of gold colloids through the MIP's thiol groups, and (3) trapping of the MIP microspheres i

58 bound NHS groups, oxidation of some resident thiol groups, and deposition of adventitious hydrocarbon

59 The modification is associated with the thiol groups, and only such modified protein species par

60 ermini are selectively converted to reactive thiol groups, and the thiol-containing N-terminal peptid

61 xyuridine derivatives that carry a protected thiol group appended via different linkers containing ei

62 versatile methods for the quantification of thiol groups are of considerable interest not only for p

63 Thiol groups are preferentially modified, supporting the

64 At neutral pH, however, >99% of DTT thiol groups are protonated and thus unreactive.

65 zed with discrete pairs of sulfonic acid and thiol groups are reported.

66 ribed in vivo, possibly because most protein thiol groups are strongly buffered against oxidation by

67 sulfide, eight low molecular mass thiols and thiol groups associated with natural organic matter (NOM

68 e c(2), but this interaction requires a free thiol group at apocytochrome c(2) heme binding site.

69 are oligonucleotide molecules labeled with a thiol group at one end and a fluorophore at the other.

70 cation results revealed overoxidation of the thiol group at position 315 to sulfonic acid occurring v

71 s allowed us to manipulate the properties of thiol groups at position 631 and correlate side-chain pr

72 The unusual presence of a pendant thiol group bound to one Mn(II) ion in Mn(II)2SH is evid

73 of Cd(2+) or GSH with a blocked, S-alkylated thiol group, but is also necessary for net PC synthesis.

74 pathways involved in the modification of the thiol group by S-nitrosothiols is important for understa

75 Modification of cysteine thiol groups by inducers in the linker region of Kelch-l

76 S-Nitrosylation of protein thiol groups by nitric oxide (NO) is a widely recognized

77 ection of NDBF render it superior to Bhc for thiol group caging.

78 The X-ray structures show that the thiol group chelates the active site zinc, the carboxyli

79 iquid-phase silanization, (1.3-9.0) x 10(12) thiol groups/cm2 on the glass samples were bound.

80 Low concentrations of thiol groups completely inactivated silver, while methyl

81 s (Ras) by S-nitrosylation of a redox-active thiol group (Cys(118)).

82 wo of its six exoplasmic cysteines have free thiol groups (Cys251 and Cys384).

83 s work had shown the existence of a reactive thiol group, cysteine 726, whose alkylation led to loss

84 The pKA values for a given thiol group depend on the position of the cysteine resid

85 A fullerene derivative 10 with a terminal thiol group dissolves easily in common organic solvents

86 d from 6.4 in wt to 5.5, indicating that the thiol group elicits an acidic pK shift.

87 c constructs which bear strategically placed thiol groups, enabling native chemical ligation.

88 gestions that complex formation with organic thiol groups enhances the rate of MeHg photodegradation,

89 Here, we extend HX theory to model thiol group exchange (SX) in single cysteine-containing

90 nus and with Alexa 546 maleimide at the free thiol group, followed by conversion to MT containing onl

91 rough covalent binding at its cysteine (Cys) thiol group, followed by stepwise catalyzed degradation

92 veal a remarkable binding specificity of the thiol group for the sulfur-rich {100} and {110} faces of

93 glutathione-like peptides containing blocked thiol groups for activity.

94 nes were synthesized and functionalized with thiol groups for single-molecule electrical measurements

95 ed of a tripodal linker with three protected thiol groups for surface attachment.

96 als stabilized with thiol ligands or bearing thiol groups for the subsequent (bio-) functionalization

97 The thiol group from cysteine in the peptide aptamer, i.e.,

98 -ordinated by the tetrahedral arrangement of thiol groups from four cysteine residues.

99 fication responses involving complexation by thiol groups from peptides.

100 deficiency responses such as the release of thiol groups from the S storage sources.

101 cetylthio)acetyl]-(D-Phe)-Phe-Arg-CH2Cl; the thiol group generated subsequently on the incorporated i

102 or from histones in which the two H3 Cys 110 thiol groups have been oxidized to form a disulfide brid

103 d nanoparticles were attached via the distal thiol groups, (ii) formation of self-assembled monolayer

104 E. coli proteins that harbour H2O2-sensitive thiol groups, implying that reactive oxygen and nitrogen

105 The thiol group in LHP directly binds with gold nanoparticle

106 ollectively, these findings suggest that the thiol group in NAC is required for its effects on glial

107 Substrate analogs incorporating a primary thiol group in place of the primary alcohol group in nor

108 of human apo-S100A1 protein with the Cys(85) thiol group in reduced and S-nitrosylated states.

109 Reduction exposed the native thiol group in the antibody that readily chemisorbed ont

110 ligand that is replaced by the homocysteine thiol group in the enzyme-substrate complex.

111 t of 0.64, reconfirming the involvement of a thiol group in the mechanism.

112 Thiol groups in biological molecules play a significant

113 Measurements of the pK(a)s for thiol groups in free and bound peptide indicate that pep

114 Thiol groups in HIF-1 or in proteins that modify HIF-1 a

115 Once the oxidized thiol groups in IscA are re-reduced with the thioredoxin

116 peroxide appears to oxidize the iron binding thiol groups in IscA, thus blocking the iron binding in

117 in crystalline mercury sulfides or bound to thiol groups in macromolecular natural organic matter.

118 accessibility of charged MTS reagents to the thiol groups in mutants of TM III, it appears that TM II

119 e residues, Cys476 and Cys489, exist as free thiol groups in oxidized AhpF and play no role in cataly

120 urthermore, NaHS decreased the ratio of free thiol groups in p65, whereas the thiol reductant DTT rev

121 ced and forms reactive products that bind to thiol groups in proteins, peptides, and amino acids.

122 assaying mercury derivatization of cysteinyl thiol groups in proteins.

123 Prior alkylation of the cysteine thiol groups in reduced rSeBP prevented selenite reducti

124 n dipicolinic acid diamide was equipped with thiol groups in the amidic side arms.

125 ial containing randomly distributed acid and thiol groups in the condensation of acetone and phenol t

126 Cu(+) proximal to the conserved carboxyl and thiol groups in the entrance site that induce metal rele

127 ears to be related to direct modification of thiol groups in the NF-kappaB subunits.

128 -spirobifluorene with three acetyl protected thiol groups in the positions 2, 3' and 6' for depositio

129 Differential chemical modification of thiol groups in the presence and absence of either reduc

130 ed by immobilizing Au nanoparticles onto the thiol groups in the sol-gel silicate network.

131 a provides strong evidence that the reactive thiol groups, in particular the thiols of the CXXC motif

132 hytochemical agents, all of which react with thiol groups, induce the phase 2 response through their

133 ly reduced the swelling and the oxidation of thiol groups induced by calcium ions.

134 covalently binds to vicinal protein cysteine thiol groups, induces Mt1 with a magnitude of higher pot

135 ion of the disulfide bond leaves behind free thiol groups inside the nanopores of polystyrene thin fi

136 2-iminothiolane (2-IT) is used to introduce thiol groups into proteins and peptides by reactions of

137 realized by quantitatively transferring the thiol groups into S-nitrosothiol functionalities.

138 g an adenylate kinase mutant, possessing two thiol groups, into HPMA copolymer- or PEG-based hydrogel

139 The number of thiol groups introduced on glass substrates were measure

140 66 subunit is very weak, indicating that the thiol group is disordered, presumably because there is n

141 The C73 thiol group is exposed by a low-energy fluctuation that

142 The thiol group is protected with a 2-cyanoethyl group and t

143 and the complete ligand coverage by aromatic thiol group is shown by NMR.

144 relationship (SAR) studies revealed that the thiol group is the pharmacophore of the natural product.

145 ing organized pairs of arylsulfonic acid and thiol groups, is significantly more active than the alky

146 thiolates are far stronger nucleophiles than thiol groups, it is generally accepted that cysteine-bas

147 ss spectrometric analysis, titration of free thiol groups, kinetic studies of irreversible inhibition

148 on of masked (i.e., not directly accessible) thiol groups like disulfides such as lipoic acid and thi

149 '-bearing) onto the NP surface via maleimide/thiol group-mediated covalent bonding improves the macro

150 hods, and methods that rely on acyl chain or thiol group modification for acyl CoA ester detection.

151 and NaB[3H]4 was inhibited by ADP, ATP, and thiol group modifying reagents.

152 f a glucose oxidase enzyme to display a free thiol group near its active site.

153 if their disulfide bonds are reduced to free thiol groups [NR1(C744,C798); NR2(C87,C320)].

154 Glycosylation of the free thiol group of 17, 25, or 26, using trichloroacetimidate

155 10h and functionalized by reaction with the thiol group of 4-aminothiophenol and Hb was also reacted

156 -(dimethylamino)naphthalene] attached to the thiol group of a cysteine introduced at position 17 of C

157 es the formation of a covalent adduct of the thiol group of a functional cysteine in the cofactor-bin

158 d both suggested possible involvement of the thiol group of another cysteine residue in ThiI.

159 lpha,beta-unsaturated carbonyl moiety to the thiol group of calpain's catalytic Cys115 residue by a M

160 The proximity of its thiol group to the thiol group of CoA derived from superimposed models of t

161 tes minimally to the rate increase since the thiol group of CoA lends over 40 kJ/mol to the reaction,

162 the enzyme-bound Ile-AMP and Ile-tRNA to the thiol group of coenzyme A, forming a thioester, Ile-S-Co

163 The absence of the thiol group of Cys 160 in the variants C160S and C160A d

164 The free thiol group of Cys(121) turned out to be the major bindi

165 Thus, the pK(a) values for the thiol group of Cys(31) and Cys(34) are 4.8 and 11.3, res

166 In the ternary reactant complex, the thiol group of Cys-21 of the peptide is facing Asp-166 a

167 The thiol group of Cys-269 was covalently attached to the di

168 e quinine ring is covalently attached to the thiol group of Cys115, the molecular target of the antib

169 HBY 097 makes a hydrogen bond with the thiol group of Cys181 that helps the drug retain potency

170 ted mutagenesis experiments suggest that the thiol group of Cys250, a residue found only in algal APS

171 Co-ordination of zinc to the thiol group of cysteine allows mobilization of zinc thro

172 by targeting reactive moieties, such as the thiol group of cysteine or the C-2 position of tryptopha

173 ion through the amine group of lysine or the thiol group of cysteine residues yields heterogeneous pr

174 functional groups, actually reacted with the thiol group of cysteine when in proximity.

175 one (GSNO) promoted S-glutathionylation of a thiol group of GAPDH both in vitro and under cellular co

176 As(III) transport, indicating that the free thiol group of GSH is required.

177 arily by formation of disulfide bonds at the thiol group of its terminal cysteine.

178 lfide bond of high reduction potential and a thiol group of low pKa.

179 old nanoparticles (AuNP) surface through the thiol group of native or introduced cysteine residues.

180 One main in vivo target of ROS is the thiol group of proteins.

181 e cysteine residue in the sequence, with the thiol group of the cysteine residue attached to the C-te

182 ace of the CdSe/ZnS quantum dots through the thiol group of the peptide cysteine residue.

183 th ligands were covalently bound by the free thiol group of the protein, whereas the affinity for all

184 at pH values where the more acidic cysteine thiol group of the reduced proteins would be expected to

185 Second, the thiol group of the released dipeptide reduces ferric to

186 nding to HSA was abolished when the terminal thiol group of this complex was absent.

187 The redox potential for oxidation of the two thiol groups of Ac(gamma-Glu-Cys)2-NH2 to form an intram

188 as catalytically active, indicating that the thiol groups of Cys(82) in the active molecules may be d

189 f nitric oxide (NO)-related species with the thiol groups of cysteine residues 83 and 157, to form SN

190 ological effects directly by binding to free thiol groups of cysteine residues in a chemical reaction

191 carbonic anhydrase linked chemically through thiol groups of cysteine residues introduced by site-dir

192 ups of heme b (protoporphyrin IX-Fe) and the thiol groups of cysteines at their conserved heme bindin

193 Oxidation of thiol groups of cysteines by reactive oxygen, generated

194 VICAT reagents tag thiol groups of cysteines or thioacetylated amino groups

195 our-carbon sugar threose, indicates that the thiol groups of DTT are required for inhibition, and als

196 nalization of mPEG using the reaction of the thiol groups of glutathione, dithiothreitol, and hemoglo

197 oroborate (BF4NO), a NO+ donor, modified the thiol groups of glyceraldehyde-3-phosphate dehydrogenase

198 activates TRPC6 channels via modification of thiol groups of intracellular proteins.

199 ties of the most reactive of the 25 cysteine thiol groups of Keap1 have been determined by tritium in

200 rcurial chromatography to capture accessible thiol groups of proteins at (or near) nascent repair sit

201 pare and reacts very rapidly with thiols and thiol groups of proteins to give corresponding S-nitroso

202 ion, in part, by S-nitrosylating active site thiol groups of proteins.

203 Despite its diffusible nature, NO modifies thiol groups of specific cysteine residues in target pro

204 oxidation-reduction chemistry involving the thiol groups of the cysteine (Cys) residues.

205 The enormous range of reactivity of the thiol groups of the cysteinyl residues in proteins and t

206 functionalities react readily with amine and thiol groups of the enzyme to form stable covalent bonds

207 The direct interaction of this TP with thiol groups of the Keap1 sensor for inducers is demonst

208 s paralleled the titration of the respective thiol groups of the reducing substrates, consistent with

209 the formation of covalent bonds between the thiol groups of two cysteines residues at the heme-bindi

210 ns can compete with one another for the same thiol group on a single cysteine residue, forming a mole

211 act as a Michael acceptor and react with the thiol group on C319 of RAD51, using a conjugate addition

212 the Co-C5' bond occurs in the absence of the thiol group on Cys 408.

213 y interacting with Cys 744 leading to a free thiol group on Cys 798 and subsequent persistent activat

214 A single thiol group on Cys152 reacts with the alpha,beta-unsatur

215 The sulfhydration of free thiol group on cysteine 38 in p65 served as a molecular

216 f a Zn(3)Fb(3) cyclic hexamer containing one thiol group on each porphyrin was prepared on a gold ele

217 uggest that synthetic schemes that combine a thiol group on one end of a molecule with a group, R, to

218 The terminal cysteine thiol group on the PNA peptide backbone is reacted with

219 c oxide (NO)-related species with a cysteine thiol group on the target protein.

220 t catalyzes disulfide bond formation between thiol groups on cysteine residues.

221 10 microM) selenite can react with essential thiol groups on enzymes to form RS-Se-SR adducts with re

222 x titrations demonstrate that the regulatory thiol groups on gamma(2)-ATP synthase remain reduced und

223 n and doxorubicinol reduced the abundance of thiol groups on RyR2, further indicating that oxidation

224 reagents and oxidative stress may modify two thiol groups on the ANT and thus stimulate pore opening

225 The thiol groups on the MIP surface allow the microspheres t

226 Blocking of the protein thiol groups on the MPI by N-ethylmaleimide (NEM) marked

227 The latter react with thiol groups on the surface, producing thioether links b

228 anaerobic conditions required four cysteine thiol groups, one on each subunit.

229 Furthermore, it was found that placement of thiol groups onto an array with the Chan-Lam reaction us

230 or the quantification of directly accessible thiol groups or ligands on the surface of 2D- and 3D-sup

231 carboxylic acid groups, 12 amidino groups, 6 thiol groups, or 6 thiol groups and 6 carboxylic acid gr

232 s: binding to humic/fulvic acids, binding to thiol-groups, or a combination of both.

233 orite-mediated fluorescein bleaching and BSA thiol groups oxidation, whilst in living cells its effec

234 Thiol-group oxidation of active and allosteric cysteines

235 A polyallylamine bisphosphonate with latent thiol groups (PABT), (2) a polyethyleneimine (PEI) with

236 s functionalized with alkylsulfonic acid and thiol group pairs have been shown to catalyze the synthe

237 Thiol groups play a significant role in various cellular

238 good yields (42-70%) by the photoaddition of thiol groups, positioned at the anomeric centers of the

239 based structure predictions suggest that the thiol groups present are solvent-exposed on a single pro

240 Oxidation/reduction reactions of protein thiol groups (PSH) have been implicated in many physiolo

241 pproximately four of the eight co-ordinating thiol groups release protons with zinc uptake, in agreem

242 Surface hydrophobicity and accessible thiol groups remained nearly unchanged after HPLT treatm

243 t enhances the nucleophilic character of the thiol group required for glutamine hydrolysis.

244 elating with the loss of four and one to two thiol groups, respectively, confirming the thiols as tar

245 single mutants, in which substitution of the thiol group resulted in a reduced k(cat) (to 26-33% of t

246 Oxidation of S100B's thiol groups resulted in the formation of oligomers that

247 sulting from the modification (reduction) of thiol group(s) in the glucose transport protein(s).

248 em to specifically sensitize IP3Rs through a thiol group(s) within the IP3R, which is probably inacce

249 Redox reactions involving these two thiol groups sensitize other NMDAR sites to S-nitrosylat

250 A catalyst having acid and thiol groups separated by three carbon atoms is ca. 3 ti

251 eplaced Arg57 with Cys to introduce a unique thiol group (-SH) in our model peptide.

252 ons (OC-DPCs) were first functionalized with thiol groups (-SH) and then immobilized with gold nanopa

253 Here, we discuss how thiol groups (-SH) naturally present on the cell surface

254 The free thiol groups so produced interact with gold lamina makin

255 tantially by the presence of a terminal-free thiol group, such as a Cys residue, primarily due to bet

256 high levels of cysteine residues and vicinal thiol groups, such as promyelocytic leukemia protein (PM

257 octa-3,6-diene-2, 8-dione, which cross-links thiol groups that are within 3-6 A of each other.

258 rboxylethyl) phosphine liberated the desired thiol groups that bind the first layer of gold nanoparti

259 tures (TDNs) with site-specifically modified thiol groups that can be readily anchored on the surface

260 study identifies two classes of redox-active thiol groups that form disulfide bonds upon oxidation.

261 ide has two ends of featuring carboxylic and thiol groups that react with UCNPs and AuNPs, and the re

262 Furthermore, since they target the cysteine thiol group, the presence of these artifacts will inevit

263 The studies of thiol group titration and irreversible kinetic experimen

264 The proximity of its thiol group to the thiol group of CoA derived from super

265 ts as a primary proton acceptor from the GSH thiol group to transfer the proton to His107.

266 directly utilizing highly reactive cysteine thiol groups to elicit hydroperoxide reduction.

267 eversible oxidative modification of cysteine thiol groups to form cysteine S-sulfenic acids.

268 Many of these platforms rely on thiol groups to tether DNA to gold surfaces, but this me

269 NA oligomer (modified at its terminus with a thiol group) to an aminosilane film formed on silica sur

270 , non-functionalised and functionalised with thiol groups, to inhibit PPO activity in the model syste

271 n modulating the reactivity of RsrA cysteine thiol groups towards oxidation.

272 To probe biological utility, thiol group uncaging was carried out using a peptide der

273 ural changes of S100B after oxidation of its thiol groups under denaturing and nondenaturing conditio

274 xide (NO.) does not react significantly with thiol groups under physiological conditions, whereas a v

275 ng a pyridazoresorcinol chelator and protein thiol groups using 4,4'-dipyridyl disulfide has establis

276 amino-3'carboxylb iphenyl, in which the free thiol group was replaced with a 1-(4-cyanobenzyl)imidazo

277 se silanization, the number of surface-bound thiol groups was found to be dependent on both postsilan

278 The reactivity of these thiol groups was very sensitive to oxidation by naphthoq

279 ent during the dough stage that insufficient thiol groups were available for forming dough layer inte

280 Free thiol groups were identified as an internal source of el

281 behaved like the wild-type channel when the thiol groups were in the reduced state.

282 Peptides and proteins containing free thiol groups were labeled with OND electrophiles with hi

283 These findings suggested that distinct thiol groups were modulated by these two agents.

284 Thiol groups were nonetheless not found directly associa

285 pines, and electrochemical derivatization of thiol groups were used to demonstrate the performance of

286 e number of surface-bound, chemically active thiol groups, were investigated using a design of experi

287 ity for 4-OHEN; Cys 47 was the most reactive thiol group whereas Cys 169 was resistant to modificatio

288 (PTPases) feature an essential nucleophilic thiol group which attacks the phosphorus atom in a subst

289 int of the dendron ligands is chosen to be a thiol group which is a universal coordinating site for c

290 significantly (30-90%) oxidatively modified thiol groups, which appear to be specifically sensitive

291 mplementary DNA oligonucleotides capped with thiol groups, which bind to gold.

292 ve disulfide bonds in antibodies to generate thiol groups, which then are labeled using thiol-reactiv

293 ral fluctuations preferentially expose their thiol groups, while keeping their disulfide bonds buried

294 The EPR effects of blocking the thiol group with N-ethyl-maleimide and using carboxypept

295 explained by a tight interaction of the CoA thiol group with the side chains of aromatic residues, w

296 Subsequent protection of the side chain thiol group with trityl alcohol and alpha-amine function

297 method relies on the reversible labeling of thiol groups with biotin and exploitation of the ultrast

298 Oxidizing thiol groups with H2O2 or modifying them with MTSET or M

299 For this reason, only accessible protein thiol groups with high thiol-disulfide oxidation potenti

300 nanoparticles (i.e., surface complexation of thiol groups with the iron atoms) is likely to be respon