ライフサイエンスコーパス: tryptic peptide

1 ning basic amino acid residues (for example, tryptic peptides).

2 using LC-MS/MS for detection of a selective tryptic peptide.

3 +0) to six amino acid residues (+6) for each tryptic peptide.

4 to enhance MALDI tandem mass spectrometry of tryptic peptides.

5 ication of isoforms of threonine residues in tryptic peptides.

6 -activated dissociation (CAD) spectra of the tryptic peptides.

7 observed for arginine- and lysine-terminated tryptic peptides.

8 rified protein, and LC-MS/MS analysis of CRP tryptic peptides.

9 ne product by mass spectrometric analysis of tryptic peptides.

10 uorophore based on mass spectral analysis of tryptic peptides.

11 reaction with C-terminal digestion to modify tryptic peptides.

12 nalysis of typically much smaller unmodified tryptic peptides.

13 -spectrometric analysis of their constituent tryptic peptides.

14 terns for singly charged Arg- and Lys-ending tryptic peptides.

15 724-739) were identified as isoform-specific tryptic peptides.

16 n the intense y series peaks associated with tryptic peptides.

17 the ion current ratio determined for the two tryptic peptides.

18 f-flight mass spectrometry (MALDI-TOF MS) of tryptic peptides.

19 LIC models developed for complex mixtures of tryptic peptides.

20 identified as Pg by mass spectrometry of its tryptic peptides.

21 cluded an estimated approximately 98% of all tryptic peptides.

22 ibed for a collection of approximately 40000 tryptic peptides.

23 ntified in acidic fractions from analysis of tryptic peptides.

24 bearing characteristics very different from tryptic peptides.

25 s to compare yields of numerous varieties of tryptic peptides.

26 tation and by mass spectroscopic analysis of tryptic peptides.

27 es of elastase to specifically target larger tryptic peptides.

28 block both N-termini and lysine residues of tryptic peptides.

29 and more sequence information for the large tryptic peptides.

30 ing site for an inhibitor located within the tryptic peptide (128)AACWWAGIK(136) was identified.

31 wing the formation of the bis-phosphorylated tryptic peptide, 173-HTDDEMT*GY*VATR-186, using [gamma-3

32 Two unique deglycosylated tryptic peptides, (21)EAENITTGCAEHCSLNENITVPDTK (45) (T

33 etylated amino groups and introduce into the tryptic peptide a biotin affinity handle, a visible moie

34 has been demonstrated with a triply charged tryptic peptide, a triply charged tryptic phosphopeptide

35 s been demonstrated with a doubly protonated tryptic peptide, a triply protonated phosphopeptide, and

36 Levels of the tryptic peptide ALFDFLK, found in the schizophrenia risk

37 onditions and analyzing the MS/MS spectra of tryptic peptides allow an easy and high-throughput asses

38 oaches using selected reaction monitoring of tryptic peptides (also known as bottom up) have become c

39 d substrate ssDNA bind to the same three A3G tryptic peptides (amino acids 181-194, 314-320, and 345-

40 a combination of protein mass spectrometry, tryptic peptide analysis, and (32)P radiolabeling.

41 meTools synthetic peptide library to 550,000 tryptic peptides and 21 million high-quality tandem mass

42 hout enrichment of glycopeptides from global tryptic peptides and at a false discovery rate of 1%, 10

43 as obtained using PACE-MSI for both digested tryptic peptides and endogenous neuropeptides from compl

44 sylation sites were separated from all other tryptic peptides and identified using MS data.

45 MS and MS/MS spectra of BR tryptic peptides and intact protein were generally super

46 tion, MALDI-ToF mass fingerprint analysis of tryptic peptides and MALDI-ToF reflectron in-source deca

47 By isolating the tryptic peptides and subjecting them to Edman sequence a

48 abundance by counting the number of detected tryptic peptides and their corresponding MS spectra.

49 sing mass spectra of the cysteine-containing tryptic peptides and used to follow the unfolding of eac

50 cal lengths (e.g. shorter/longer than common tryptic peptides) and lack of tryptic residues to facili

51 )(1%)) of 20.2 and 20.5, common sequences of tryptic peptides, and cross-reactivity with FAP antibody

52 tein sequence up to 28 residues, overlapping tryptic peptides, and cyanogen bromide (CNBr) peptides.

53 atographic fractionation of the ICAT-labeled tryptic peptides, and protein identification and quantif

54 sotopic tags to both the N- and C-termini of tryptic peptides, and second, a search engine (based on

55 nal activation of modified lysine-terminated tryptic peptide anions is consistent with a covalent mod

56 in 50 min from approximately 4000 identified tryptic peptides; approximately 550 proteins in 20 min f

57 The effective peak capacities in analyses of tryptic peptides are approximately 500 for FAIMS/IMS sep

58 d y-ion series, and LC retention time of the tryptic peptides are essential pieces of information for

59 Tryptic peptides are generated from tissue foci by apply

60 We hypothesize that non-tryptic peptides are mainly created from the truncation

61 r and, because cysteine residues on separate tryptic peptides are measured separately, is not complic

62 metry (ESI-tandem MS), a total of 6112 fully tryptic peptides are sequenced at a 1% false discovery r

63 Stable-isotope-labeled (tryptic) peptides are spiked into digested protein sampl

64 g synthetic heavy isotope-labeled C-terminal tryptic peptides as spiked standards with a triple quadr

65 ed multiple reaction monitoring quantitative tryptic peptide assays were developed for each phosphory

66 s generated containing 8400 MS/MS spectra of tryptic peptides assigned with high probability to an am

67 ed that phosphorylation occurred on a single tryptic peptide at Ser-174.

68 tein and the few hydrophobic and hydrophilic tryptic peptides available in the digest is demonstrated

69 s in the mass spectra of this doubly charged tryptic peptide, based solely on its amino acid sequence

70 ainly created from the truncation of regular tryptic peptides before separation.

71 responding increase in molecular mass of the tryptic peptide by 136 Da.

72 2SC formation were determined by analysis of tryptic peptides by high-performance liquid chromatograp

73 teins and direct detection of lipid-modified tryptic peptides by mass spectrometry.

74 n this study, we optimized a method to image tryptic peptides by matrix-assisted laser desorption ion

75 sp. NRC-1 and identified the sequence of 23 tryptic peptides by nano-liquid chromatography electrosp

76 ry was performed on several of the resulting tryptic peptides by using collision quadrupole time of f

77 that the MALDI MS/MS analysis of sulfonated tryptic peptides can provide a highly effective method f

78 Stable isotopically labeled (SIL) tryptic peptides, cleavable SIL peptides, and a full-len

79 man degradation and liquid chromatography of tryptic peptides combined with tandem mass spectrometry

80 ed the mass distributions of all theoretical tryptic peptides composed of 20 natural amino acids and

81 ein concentration was shown to be unequal to tryptic peptide concentrations for most peptides, includ

82 crophages is phosphorylated on only a single tryptic peptide containing 14 potential phosphoacceptors

83 ptides, MALDI MS/MS analysis of a sulfonated tryptic peptide containing a diglycine branch generates

84 Further, the tryptic peptide containing the active center serine of A

85 ometry (LC-MS) with tandem MS (MS/MS) of the tryptic peptide containing the intramolecular disulfide

86 and asymmetric cleavage of disulfide-linked tryptic peptides containing Cys-99 and Cys-450.

87 tial analysis of 20 samples containing 10 ng tryptic peptides demonstrated high reproducibility with

88 Mass spectral analysis of tryptic peptides derived from human ADAMTS13 indicate th

89 the analysis of coeluting model peptides and tryptic peptides derived from human plasma proteins, all

90 no acid pools in barley leaves and then into tryptic peptides derived from newly synthesized proteins

91 ptimize quantitation of different amounts of tryptic peptides derived from PE using light (H4, 4 hydr

92 upported by a mass loss of 2 Da observed for tryptic peptides derived from species that accumulate du

93 When the mass defects of tryptic peptides derived from the human proteome are plo

94 LDI-TOF mass spectrometric fingerprinting of tryptic peptides derived from the purified NEC3 confirme

95 spray ionization-tandem mass spectrometry of tryptic peptides derived from whole cell digests.

96 pproach simplified the detection of glycated tryptic peptide elution in the LC/MS analysis by giving

97 ine resolve four distinct sets of Abeta17-28 tryptic peptide epimers on a rapid (~1 s) time scale.

98 CID as the unmodified cations for the small tryptic peptides examined here and more sequence informa

99 ities that are used to predict the number of tryptic peptides expected to be detected for one molecul

100 to analysis by MALDI-TOF mass spectrometry, tryptic peptide fingerprinting, molecular characterizati

101 ography tandem mass spectrometry analysis of tryptic peptides, followed by searching an appropriate s

102 ial QconCAT proteins that are concatamers of tryptic peptides for several proteins.

103 artificial proteins that are concatamers of tryptic peptides for several proteins.

104 ne strong cation exchange chromatography for tryptic peptide fractionation and combining it with the

105 Tryptic peptides fragment in ion trap tandem mass spectr

106 For the tryptic peptides, fragmentation is localized at the ends

107 intact proteins and/or an LC-MS analysis of tryptic peptide fragments generated after the oxidation

108 ectrometry/mass spectrometry analysis on the tryptic peptide fragments indicates that the 3-fluorosia

109 The tryptic peptide fragments of this phosphoprotein were se

110 proteins are generally characterized through tryptic peptide fragments, this paper reports a method f

111 onfirmed using the y14 ion and b8 ion of the tryptic peptide from bovine Hb alpha chain residues 69-9

112 nfolded and deamidated ribonuclease A, and a tryptic peptide from calmodulin deamidated in its native

113 dues 69-90, and HML was quantified using the tryptic peptide from human Hb alpha chain residues 63-91

114 A tryptic peptide from Tm*146-TnI with a molecular mass of

115 eamidated tryptic peptide of cytochrome c, a tryptic peptide from unfolded and deamidated ribonucleas

116 fidence identifications of >12 000 different tryptic peptides from >2000 distinct Shewanella oneidens

117 ent sequencing approach, a collection of 266 tryptic peptides from 23 model proteins were analyzed an

118 In the analysis of 31 tryptic peptides from 4 model proteins, the algorithm id

119 Separating tryptic peptides from [(32)P]orthophosphate-labeled cell

120 Tryptic peptides from a 250-kDa immunoprecipitated prote

121 btained by partial sequencing of distinctive tryptic peptides from Bacillus spores via post-source de

122 Through a PACE separation, 46 tryptic peptides from bovine serum albumin and 150 putat

123 esulting peptide anions, as demonstrated for tryptic peptides from bovine serum albumin and Halobacte

124 y, was evaluated using a mixture composed of tryptic peptides from caseins, bovine serum albumin, and

125 ed deamidation half-life for three different tryptic peptides from collagen (I) ranged from 2000 to 6

126 proteomics analyses to confidently identify tryptic peptides from complex mixtures of proteins, as w

127 Tryptic peptides from each spot group were analyzed in d

128 s of samples of complex mixtures composed of tryptic peptides from human and mouse blood proteins usi

129 even (15)N-labeled QconCATs that cover seven tryptic peptides from human clusterin with a length of n

130 s illustrated by examination of a mixture of tryptic peptides from human hemoglobin.

131 samples containing approximately 100 mug of tryptic peptides from mouse cerebrocortical brain tissue

132 oteins isolated from the mutants showed that tryptic peptides from phycocyanin that included Asn72 we

133 gradation and mass spectrometric analyses of tryptic peptides from rat DSP-PG, along with substitutio

134 On mass spectrometric analysis of tryptic peptides from recombinant secreted human punctin

135 Mass spectrometric analysis of tryptic peptides from the cross-linked product revealed

136 ional nano-LC-ion mobility-TOF separation of tryptic peptides from the Drosophila proteome.

137 By calculating the masses of all potential tryptic peptides from the human proteome, we show that r

138 five pH bumps were applied to elute E. coli tryptic peptides from the monolith, followed by analysis

139 LC-MALDI-TOF/TOF MS analysis of tryptic peptides from the SCX fractions of an E. coli ly

140 derivatives and the production of different tryptic peptides from the unmodified and modified versio

141 Analysis of tryptic peptides from various fractions further confirme

142 For this purpose, tryptic peptides from whole cell lysates were analyzed b

143 C) was demonstrated from as little as 25 mug tryptic peptides from whole cell lysates.

144 xamined as a means of separating mixtures of tryptic peptides (from myoglobin and hemoglobin).

145 Differential dimethyl labeling of tryptic peptides generated from the purified therapeutic

146 from 27 different peptides (22 of which are tryptic peptides) has been studied in a 3D quadrupole io

147 Modified arginine-terminated tryptic peptides have shown evidence of a covalent modif

148 This approach involves (18)O labeling of tryptic peptides, high-efficiency enrichment of cysteine

149 introduce the notion of truncatability of a tryptic peptide, i.e. the probability of the peptide to

150 ithin a searching time comparable to that of tryptic peptide identification.

151 E to the mobile phase of nLC/MS experiments, tryptic peptide identifications increased from 93 to 111

152 ble-isotope-labeled standard for every ricin tryptic peptide in the sample.

153 eries of epitope sequences concatenated with tryptic peptides in a single artificial protein to creat

154 sured both the quantity and kinetics of SP-B tryptic peptides in tracheal aspirate samples of symptom

155 All tryptic peptides including N-terminal, C-terminal, and m

156 g in mass from 400 to 3000 m/z) of model and tryptic peptides, including serine, threonine, and tyros

157 LC-MS analysis of nonreduced tryptic peptides indicated trisulfide bonds are associat

158 ated that serine phosphorylation of a single tryptic peptide inhibits its transport activity without

159 157 nm photodissociation of a singly charged tryptic peptide ion (NWDAGFGR) showed that prompt photof

160 tructural changes that would be expected for tryptic peptide ions and are consistent with the experim

161 ss spectrometry (IMS-MS) study revealed that tryptic peptide ions containing a proline residue at the

162 ser desorption/ionization (AP-MALDI)-derived tryptic peptide ions have been subjected to ion/ion reac

163 roteomic analysis, yet the singly protonated tryptic peptide ions produced by MALDI are significantly

164 viously been shown that photodissociation of tryptic peptide ions with 157 nm light in a matrix-assis

165 y antipeptide antibodies, wherein a specific tryptic peptide is selected as a stoichiometric represen

166 Searching for all potential non-tryptic peptides is, however, time consuming for shotgun

167 d amount(s) of standard peptides (PE-derived tryptic peptides) is necessary for high-quality linear q

168 Further analysis on tryptic peptides led us to conclude that a single glycos

169 study the peptide QPSSSR, a very hydrophilic tryptic peptide located on the C-terminus of the G prote

170 to conventional tandem MS spectra of native tryptic peptides, MALDI MS/MS analysis of a sulfonated t

171 The tryptic peptide map (mass spectral analysis) revealed th

172 A tryptic peptide map identified two isoAsp-containing pep

173 Tryptic peptide mapping and MALDI-MS verify labeling at

174 Using tryptic peptide mapping and mutagenesis, we have identif

175 Tryptic peptide mapping and tandem mass sequencing were

176 Tryptic peptide mapping and tandem mass spectrometry of

177 romatography, were fully characterized using tryptic peptide mapping and tandem mass spectrometry.

178 n was modified minimally with methylglyoxal, tryptic peptide mapping indicated a hotspot of modificat

179 Tryptic peptide mapping showed that the CpcSU-dependent

180 s as a tool to increase sequence coverage in tryptic peptide mapping.

181 rom cation-exchange chromatography (CEX) and tryptic peptide maps generated with the new digestion me

182 of the extracted ion chromatograms from the tryptic peptide maps.

183 The most robust tryptic peptide marker in the validation was LTLGSALAAPQ

184 LC-MS/MS pipeline to identify taxon-specific tryptic peptide markers for the identification of Salmon

185 LN-KO and wild-type hearts were subjected to tryptic peptide mass fingerprinting for identification b

186 By tryptic peptide mass fingerprinting we identified 55 pro

187 N-terminal sequencing and tryptic peptide mass spectrometry fingerprint analysis d

188 esponded to peptides that were identified by tryptic peptide mass spectrometry fingerprint analysis o

189 eptide analytes from both simple and complex tryptic peptide matrices using selected reaction monitor

190 Identifying more peptides, e.g. non-tryptic peptides, may increase the peptide coverage and

191 of the serum protein and indirectly with the tryptic peptides measured by MS.

192 ence in peptide assignments was achieved for tryptic peptides, measured by changes in DeltaCN and RSP

193 roscopy, separated protein fluorescence, and tryptic peptide modification in liquid chromatography-ta

194 For freebase guanidinated BSA tryptic peptides, more than 6-times the peptides were ob

195 Three cross-linked tryptic peptides (nucleopeptides) of hRPA70xdT(30) (T(43

196 substance P peptide, as well as a mixture of tryptic peptides obtained by enzymatic digestion of cyto

197 LC-MS/MS analysis of the tryptic peptides obtained from the in vitro ubiquitinate

198 tion in peptides from proteins; a deamidated tryptic peptide of cytochrome c, a tryptic peptide from

199 A tryptic peptide of Mrf1p, GGQHVNTTDSAVR, containing the

200 defined by the presence of the COOH-terminal tryptic peptide of the CgA precursor, corresponding to r

201 ometer and applied for the separation of the tryptic peptides of a six-protein mixture and for the pr

202 formance liquid chromatographic radiolabeled tryptic peptides of alkylated bC2GnT-M on C18 column.

203 Selected tryptic peptides of beta-Lg (ALPMHIR, LIVTQTMK and VLVLD

204 An analysis of the tryptic peptides of cytochrome c formed by both ESI and

205 the tested BGEs, the best resolution of the tryptic peptides of extracted proteins of the above thre

206 HPLC analysis of tryptic peptides of FSBA-modified enzyme revealed the pr

207 untargeted "adductomics" method detected 50 tryptic peptides of HSA, containing Cys34 and prominent

208 ay ionization time-of-flight analysis of the tryptic peptides of mononitrated lysozyme identified the

209 ds of known amounts of heavy isotope-labeled tryptic peptides of PE provided linear calibration plots

210 Selected resolved tryptic peptides of proteins were characterised by effec

211 rmance liquid chromatographic profile of the tryptic peptides of reduced-alkylated (35)S-labeled C2Gn

212 This strategy is demonstrated with the tryptic peptides of several model proteins, including tw

213 Mass spectrometry of tryptic peptides of the 15 kDa polypeptide identified it

214 romatography-tandem mass spectrometry of the tryptic peptides of the extracted/digested HU protein.

215 MS method for the direct detection of unique tryptic peptides of the KPC protein in clinical bacteria

216 Three tryptic peptides of the protein were isolated and sequen

217 ass of 2601.2 Da that was not present in the tryptic peptides of Tm*146 or TnI was identified using H

218 ion concatamer (QconCAT) carrying prototypic tryptic peptides of UCH-L1 was used as an internal stand

219 Glutamate-containing tryptic peptides of wild-type CYP4B1 were found labeled

220 lyze an interference model system comprising tryptic peptides of yeast that we contaminated with huma

221 relate the migration of 32P- and 35S-labeled tryptic peptides of ZEBRA.

222 digestion with trypsin, and stabilization of tryptic peptides on solid-phase extraction sorbent.

223 times the peptides were observed relative to tryptic peptides or those guanidinated with the conventi

224 In PAL experiments with SIRT2, a tryptic peptide originating from the covalent attachment

225 Application of this method to tryptic peptides originating from O-GlcNAcylated protein

226 exposure has been monitored by the ratio of tryptic peptide peaks that correspond to unmodified (uni

227 In the analysis of various tryptic peptides, photodissociation provided much more s

228 raction and purification were tested and the tryptic peptide pools were analysed by untargeted high r

229 oteome level by examining the quality of the tryptic peptides prepared by on-surface nanodiamond dige

230 Amino acid analysis and Edman degradation of tryptic peptides proved that the core protein for DMP1-P

231 suitable for dissociating singly protonated tryptic peptides, providing greater sequence coverage th

232 he LC/MS/MS analysis of the affinity-labeled tryptic peptides purified from HPLC, identified two majo

233 artificial gene encoding a concatenation of tryptic peptides (QCAT protein) from several chick (Gall

234 spectrometry analysis of >330,000 synthetic tryptic peptides representing essentially all canonical

235 mass spectrometry for the direct measure of tryptic peptides representing the amounts of specific pr

236 A control tryptic peptide, representing an unmodified region of FA

237 ~1000 proteins reliably using only 75 pg of tryptic peptides, representing a 10-100-fold sensitivity

238 ging from 2.4- to 12.3-fold for the detected tryptic peptides resulted; the varying response was attr

239 Extensive sequencing of tryptic peptides revealed that the 37K fragments origina

240 highest truncatability are retained for non-tryptic peptide searching.

241 roteins were then characterized by SDS-PAGE, tryptic peptide sequence analysis, and Western blot anal

242 This approach enables the invariant tryptic peptide sequences within the family to serve as

243 nd liquid chromatography (LC)-MS analysis of tryptic peptides showed that 54 peptides distributed thr

244 yptic digests were analyzed by LC-MS/MS, and tryptic peptides specific for bovine and human Hbs were

245 Hb, and equine Hb were compared, and unique tryptic peptides specific for bovine Hb, human Hb, and e

246 single artificial protein to create internal tryptic peptide standards for MS as well as an intact pr

247 by mass spectrometric analysis of protonated tryptic peptides subjected to collisional activation.

248 nd MeArg were not found together on the same tryptic peptide, suggesting reciprocal regulation of the

249 was helpful to elucidating sequences of the tryptic peptides thanks to the fragment peptide ions pro

250 itration site was determined by sequencing a tryptic peptide that included Tyr23 and Tyr20, but possi

251 ad a retention time identical to that of the tryptic peptide that includes phycocyanobilin-bound, cys

252 APP-QconCAT includes tryptic peptides that are common for all isoforms of APP

253 all isoforms of APP concatenated with those tryptic peptides that are unique for specific APP isofor

254 For the tryptic peptide, the sequence is identified with more ce

255 ause, in contrast to the more widely studied tryptic peptides, the amino acids H, K, and R were posit

256 lision Induced Dissociation (CID) spectra of tryptic peptides], their performance often deteriorates

257 creased the sequence coverage for an average tryptic peptide to 92%.

258 ion and tandem mass spectrometry analysis of tryptic peptides to identify the PAL-E antigen as a secr

259 e, and laser desorption mass spectrometry of tryptic peptides, to define a series of epidermal protei

260 s studied by analyzing the separation of the tryptic peptides under different average column pressure

261 es were driven by the spatial orientation of tryptic peptides upon interaction with the negatively ch

262 igestion, online enrichment of IL-21 derived tryptic peptides using antipeptide antibodies, and quant

263 eptides in addition to a complex mixtures of tryptic peptides using LC-MS/MS, showing not only that A

264 digestion and quantitation of a NGF-derived tryptic peptide via high-flow peptide immunoaffinity enr

265 A modified tryptic peptide was characterized with an increase in ma

266 A unique 16-mer tryptic peptide was identified by conducting capillary L

267 This tryptic peptide was quantified using a synthetic peptide

268 arge proteomic retention data set of ~30 000 tryptic peptides was collected for each 2D pairing.

269 A large-scale analysis of 755 doubly charged tryptic peptides was conducted to compare the method (ET

270 nd experimental m/z values for serum albumin tryptic peptides was found to be 8 ppm using the double

271 The retention behavior of these tryptic peptides was measured under isocratic conditions

272 In addition, in-ESI-source fragmentation of tryptic peptides was observed in this study.

273 Separation of tryptic peptides was realized using a MicroHPLC interfac

274 s spectrometry and de novo sequencing of CPO tryptic peptides, we determined that three of the seven

275 nown histone H3/H4 acetylated and methylated tryptic peptides, we identified novel H3 K18 methylation

276 plying this method to identification of semi-tryptic peptides, we show that a significant number of s

277 ated measurements for each of the endogenous tryptic peptides were 17.0, 25.4, 24.2, and 14.0% for co

278 sone mesylate and the dexamethasone-modified tryptic peptides were analyzed by mass spectrometry, and

279 When tryptic peptides were analyzed by matrix-assisted laser-

280 motifs in interacting proteins, their unique tryptic peptides were analyzed by the motif scan softwar

281 Tryptic peptides were analyzed using Thermo linear ion-t

282 The tryptic peptides were chromatographically separated with

283 The amino acid sequences of these unique tryptic peptides were confirmed by their characteristic

284 l peptide separations, a total of 6866 fully tryptic peptides were detected, leading to the identific

285 by one-dimensional gel electrophoresis, and tryptic peptides were extracted from gel slices and anal

286 In this study, tryptic peptides were generated in situ from complex spo

287 protein was purified to homogeneity, and its tryptic peptides were identified as gene At1g73080, whic

288 excised, and Ala-/Gly-rich, allele-specific tryptic peptides were identified by liquid chromatograph

289 ristics of these standards and collection of tryptic peptides were mapped into hydrophobicity index (

290 cted N-glycosylated peptides, 97% of oatp1a1 tryptic peptides were observed.

291 were digested, and evolutionarily conserved tryptic peptides were quantified using isotope-dilution

292 purified and digested with trypsin, and the tryptic peptides were separated by high pressure liquid

293 lated by denaturing gel electrophoresis, and tryptic peptides were then subjected to affinity purific

294 e determined based upon the concentration of tryptic peptides, which in turn had been quantified base

295 age intensities of spiked synthetic catalase tryptic peptides, which we used as an internal standard,

296 Derivatization of tryptic peptides with another isothiocyanate analogue, 4

297 reliably detected based on identification of tryptic peptides with masses of 1148.59 Da, 1162.60 Da,

298 This method shows generation of tryptic peptides with sequence coverage up to 90% within

299 ction; (iii) enrichment of the biotin-tagged tryptic peptides with streptavidin; (iv) liquid chromato

300 After filtering, only a limited number of tryptic peptides with the highest truncatability are ret