ライフサイエンスコーパス: peptide fragment

1 expression of a betaarr1 C-terminal-derived peptide fragment.

2 hic secreted APPalpha (sAPPalpha) and the P3 peptide fragment.

3 d trypsin enzymes on NAA-NH(2) into the heme-peptide fragment.

4 ation may prevent the formation of cytotoxic peptide fragments.

5 nize the organismal origin of unknown DNA or peptide fragments.

6 in the hydrolysis of polypeptides into small peptide fragments.

7 ion NMR, and concomitant appearance of small peptide fragments.

8 ntimicrobial defense by clustering in active peptide fragments.

9 e of proIAPP in detail by analyzing a set of peptide fragments.

10 ent for intact proteins rather than degraded peptide fragments.

11 ire processing of native proteins into short peptide fragments.

12 hat is based on the coupling of glycopeptide/peptide fragments.

13 ro, staphopain B degraded LL-37 into shorter peptide fragments.

14 hod for the total synthesis of proteins from peptide fragments.

15 d comparative mass spectrometric analysis of peptide fragments.

16 leading to the formation of Abeta and Abeta peptide fragments.

17 ave studied the characteristics of these two peptide fragments.

18 erform native chemical ligation (NCL) of two peptide fragments.

19 ide bond formation between a large number of peptide fragments.

20 uently requires proteolysis of proteins into peptide fragments.

21 as obtained through N-terminal sequencing of peptide fragments.

22 ell as circulating N-terminal and C-terminal peptide fragments.

23 '-phosphorylated pentanucleotides containing peptide fragments.

24 ased upon single-stranded DNA scaffolding of peptide fragments.

25 only a few structures of oligomers formed by peptide fragments.

26 e semisynthesis via the chemical ligation of peptide fragments.

27 ti-apoptotic N1 and the scrapie-resistant C1 peptide fragments.

28 hat generate the pathogenic or nonpathogenic peptide fragments.

29 where it cleaves food proteins into smaller peptide fragments.

30 bn-N) and the TRAP (tyrosine-rich amelogenin peptide) fragments.

31 We have used the activation peptide fragment 1.2 (F12), a ligand for anion-binding e

32 The molecular conformation of peptide fragment 105-115 of transthyretin, TTR(105-115),

33 One peptide fragment (19 amino acids) spans IGF-I residues 7

34 Synthesis and coupling of the individual peptide fragments [34 + 35 --> 51] followed by macrocycl

35 Preabsorption of the antiserum with metastin peptide fragment (45-54)-NH2 (1 microg/ml) resulted in n

36 um directed against the synthetic C-terminal peptide fragment (47-73), irBC was detected in the mouse

37 sing amino acid sequences derived from Csp24 peptide fragments, a full-length cDNA was cloned and sho

38 perature phase diagram for the amyloidogenic peptide fragment Abeta(16-22) Our results reveal that th

39 d chromatography fraction revealed two alpha-peptide fragments (alpha128-alpha139) and a heme moiety

40 ing of complex fragments, including a 20-mer peptide fragment analog of Exendin(9-39) on solid suppor

41 Peptide fragment analysis of the diagnostic peak in amni

42 ng an efficient solid phase synthesis of the peptide fragment and an effective chemoenzymatic attachm

43 esulted in the cleavage of the MB containing peptide fragment and caused a decrease in electrical sig

44 ucture of Naa50p bound to a native substrate peptide fragment and CoA.

45 d PKC-stimulated phosphorylation of the same peptide fragments and comigration of PKC-stimulated phos

46 We have identified Mtb-specific peptide fragments and developed a method to rapidly quan

47 corresponding to the carbohydrate-containing peptide fragments and large and small trypsin fragments

48 with MALDI-TOF mass spectrometry analysis of peptide fragments and peptide microsequencing, indicates

49 of the MHC class I heavy chain, an antigenic peptide fragment, and beta2-microglobulin (beta2m).

50 ences, native chemical ligation from smaller peptide fragments, and a high-throughput bacterial expre

51 sequence patterns, distinct from non-binding peptide fragments, and multi-millions of binding and non

52 -expressed T-cell receptors (TCRs) recognize peptide fragments (antigens) of pathogens bound to major

53 h analyses typically assume that a protein's peptide fragments are observed with equal likelihood, on

54 Such 10 purified peptide fragments are screened against sera from patient

55 -isotope tags and fragmented, and the tagged peptide fragments are separated by liquid chromatography

56 s in the fluorescence intensity of a labeled peptide fragment as well as a decrease in solution pH as

57 measuring the oxidation extent of different peptide fragments as a function of microwave power.

58 The resulting peptide fragment assembles into fibrils promoting the fo

59 mechanisms by which beta-amyloid (Abeta), a peptide fragment believed to contribute to Alzheimer's d

60 dentify differentially abundant proteins and peptide fragments between age groups.

61 ld SPI forms large ions identified as common peptide fragments bound to either Fmoc or the surface li

62 effective in preliminary searches for C-PTH peptide fragments, but the use of high laser power limit

63 ation of surface labeled and biotin captured peptide fragments by LC/MS/MS.

64 Here we show that peptide fragments can be exchanged by a chemoselective a

65 observations that the amino acid sequence of peptide fragments can change upon activation.

66 vealed that the CB1 C-terminal juxtamembrane peptide fragment CB1-(401-417) can directly activate the

67 nhardtii caltractin (CRC-C) and a 19 residue peptide fragment comprising the putative cdc31p-binding

68 ctional characteristics of template-directed peptide fragment condensation reactions in neutral aqueo

69 offer the promise of using this chemistry in peptide fragment condensations to produce modified pepti

70 Use of peptide fragments confirm that PrP(92-96) and PrP(107-11

71 receptor, while [ (125)I]IAC44 was found in peptide fragments consistent with labeling of both SBDLI

72 These resistant Ara h 2 peptide fragments contain intact IgE-binding epitopes an

73 This peptide fragment contained a sequence that corresponded

74 in its amino acid sequence and that a TcSSS peptide fragment containing a sequence homologous to a b

75 and RGS16 incorporated [3H]palmitate into a peptide fragment containing Cys-98, a highly conserved c

76 Moreover, we show that a CTD peptide fragment containing His-447, His-449, and Cys-45

77 A 5-kDa tryptic digest peptide fragment containing six acidic residues at posit

78 o signal, whereas the enzymatically produced peptide fragment containing the above sequence showed th

79 Finally, a short peptide fragment containing the NCX1-Met(369) cleavage s

80 We identified six peptide fragments containing 12 phosphorylated residues

81 718 and 1831, corresponding to the unlabeled peptide fragments containing the active site Tyr411 resi

82 fibrils are built by modifying the synthetic peptide fragment corresponding to residues 105-115 of th

83 tion of vectors that drive the expression of peptide fragments corresponding to their binding domains

84 cortactin Src homology 3 (SH3) domain with a peptide fragment derived from a cDNA encoding a region o

85 We previously discovered a peptide fragment derived from A46 termed VIPER (Viral In

86 tal surface with REDOR NMR show that, in the peptide fragment derived from the N-terminal 15 amino ac

87 ative cysteine with a succinimide group in a peptide fragment derived from thioredoxin-1 (Trx-1) obta

88 f high-resolution structures of CaM bound to peptide fragments derived from ion channels, there is no

89 are made up of multiple naturally occurring peptide fragments derived from semen.

90 Peptide fragments derived from the C terminus of C5a can

91 A set of peptide fragments derived from the headpiece were also c

92 ancing activity parallels the degradation of peptide fragments derived from the semenogelins (SEMs),

93 the Ru label, whereas binding of the cleaved peptide fragment devoid of Ru label reduced the ECL sign

94 to P37-42, OspA, GT, or six overlapping Arp peptide fragments did not.

95 L) method that enables efficient ligation of peptide fragments down to low nanomolar concentrations,

96 Cu(I) ligation by a Cys-rich domain peptide fragment drives the cooperative assembly of a po

97 measure the molecular weights of the tryptic peptide fragments (e.g., peptide mass mapping) and parti

98 rabbit antiserum raised against a synthetic peptide fragment encoding the unique C terminus revealed

99 ing the Rosetta fragment picker for accurate peptide fragment ensemble generation, the PIPER docking

100 uence patterns between intra-protein binding peptide fragments exist, they can be extracted using a d

101 the peptide mass fingerprint (MALDI-TOF) and peptide fragment fingerprinting (MALDI LIFT-TOF/TOF) spe

102 Peptide fragments for mass spectrometry analysis were ob

103 A key observation was that a peptide fragment formed of the first N-terminal 15 resid

104 on these regions, we focused on an antigenic peptide fragment from a disulfide bridge-bounded region

105 In contrast, a peptide fragment from domain C reduced the number of syn

106 PAPf39, a 39-residue peptide fragment from human prostatic acidic phosphatase

107 anic molecule (fluorescein), a 12 amino acid peptide fragment from the C-terminus of beta-catenin, th

108 PAPf39 is a 39-residue peptide fragment from the sequence of human prostatic ac

109 Titration of a peptide fragment from the yeast Kar1p protein to the iso

110 xpensive methodology to generate fluorescent peptide fragments from a parent sequence with diverse ch

111 toreceptor retinoid-binding protein dose and peptide fragments from conventional experimental autoimm

112 nd multi-millions of binding and non-binding peptide fragments from currently available protein X-ray

113 tration calorimetry to investigate synthetic peptide fragments from different domains of the full-len

114 Biotinylated peptide fragments from labeled proteomes are captured an

115 In semen, proteolytic peptide fragments from prostatic acid phosphatase can fo

116 However, TDP1 can only process small peptide fragments from ssDNA ends, raising the question

117 Peptide fragments from standard protein digests of bovin

118 Host cells also display peptide fragments from the host's own proteins.

119 tact tetramer, and (3) release of C-terminal peptide fragments from the intact complex.

120 Three phosphoThr peptide fragments from the kinase domain of CLV1 or BAK1

121 hr, and Tyr residues in intact proteins with peptide fragments from the same proteins.

122 peptide (2.5HIP) consisting of an insulin C-peptide fragment fused to a peptide from chromogranin A

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

124 Peptide fragments generated by collagenolysis, and the c

125 taL-crystallin was higher in the presence of peptide fragments generated from oxidized and trypsin-di

126 MALDI MS/MS analysis of peptide fragments generated from the large-diameter core

127 , isoaspartic, and aspartic acid isoforms of peptide fragments generated using trypsin.

128 erefore been necessary, for instance, on the peptide fragment GNNQQNY7-13 of yeast prion protein Sup3

129 Structural analysis of peptide fragments has provided useful information on the

130 l crystal structures of skeletal muscle RyR1 peptide fragments have been solved, but these cover less

131 The intra-protein binding peptide fragments have specific and intrinsic sequence p

132 he side chain of the self-assembling amyloid peptide fragment HHQALVFFA to give ccAQLVFFA.

133 with CD and 1D NMR studies of the 21-residue peptide fragment (HP21) derived from HP36 have shown tha

134 s work, for the first time, four human C-PTH peptide fragments, hPTH(34-84), hPTH(37-84), hPTH(38-84)

135 The four C-PTH peptide fragments identified in plasma samples from pati

136 les protein sequences from their constituent peptide fragments identified on short reads.

137 oth cell types, and amino acid sequencing of peptide fragments identified the same protein, histone H

138 antibodies against GB-generated centromeric peptide fragments identify a distinct clinical subset.

139 hat inhibit the recruitment of a coactivator peptide fragment in in vitro biochemical assays (IC(50)

140 simultaneous detection of PTHrP isoforms and peptide fragments in 30 min.

141 signature for identifying inhibitor-modified peptide fragments in complex mass spectrometry data.

142 showed that the distribution patterns of the peptide fragments in Gl-L and Gd-L were similar, but mor

143 esults suggest novel roles for ATIII-derived peptide fragments in host defense.

144 d approaches were capable of detecting C-PTH peptide fragments in human plasma at <10 pmol/L.

145 l as the presence of the individual (intact) peptide fragments in MS2 spectra.

146 , we identified over one dozen APP-generated peptide fragments in wild-type yeast (PRE1PRE2) and over

147 Tryptic peptides fragment in ion trap tandem mass spectrometry t

148 on program, it was observed that some cyclic peptides fragmented in unexpected ways resulting in the

149 eave chromogranin A into biologically active peptide fragments, including catestatin, which inhibits

150 We used recombinant MMP12 peptide fragments, including its catalytic domain, CTD,

151 ry/mass spectrometry analysis on the tryptic peptide fragments indicates that the 3-fluorosialyl moie

152 reached by using only seven short synthetic peptide fragments, instead of the 155 non-overlapping 15

153 1 at multiple sites to release transmembrane peptide fragments into the aqueous solvent.

154 ecursors, presentation requires transport of peptide fragments into the ER, but the nature of the cyt

155 site-specific integration of amino acids and peptide fragments into the homodetic cyclic peptide arch

156 nt ions to probe the components of gas-phase peptide fragment ion isomers.

157 ed by a diagnostic mass shift in one or more peptide fragment ions (for example, phosphorylation).

158 s into unused spectral space where no native peptide fragment ions exist.

159 ion and quantification of twinned peaks from peptide fragment ions in MS(2) spectra.

160 aining reagents for shifting mass defects of peptide fragment ions was systematically investigated, t

161 The ASA method successfully distinguishes peptide fragment ions with and without an FIMDL group an

162 well as for facile mass spectral analysis of peptide fragment ions with increased mass defects.

163 ctra included singly protonated peptide ion, peptide fragment ions, and peaks characteristic of the s

164 dentification of these separated proteins or peptide fragments is typically achieved by mass spectrom

165 Sequencing of peptide fragments isolated from [(3)H]CMPI-photolabeled

166 ce with the mixed GAG glycosylation of agrin peptide fragments, it was found that recombinant and in

167 e (TDP1) is a DNA repair enzyme that removes peptide fragments linked through tyrosine to the 3' end

168 type glycopeptide fraction revealed Asn-732 peptide fragments linked to the sulfoquinovose-containin

169 that exist in vertebrates, presenting small peptide fragments, lipid molecules, or small molecule me

170 ing and assembling the native structure from peptide fragments, local structures first.

171 for DnaK, examined via a short 13-mer apoMb peptide fragment matching the binding site sequence, dis

172 f spermatogenesis suggests that this laminin peptide fragment may serve as a contraceptive in male ra

173 The specific binding between short peptide fragments may provide an important driving force

174 inally, intracellular application of the MIF peptide fragment MIF-(50-65), which harbors the thiol ox

175 he biotinylated peptides and analysis of the peptide fragment mixture by nanospray liquid chromatogra

176 sis of the pepsin-induced fibrils implicates peptide fragments (named H) consisting of the 13 or 15 N

177 Furthermore, we identified several new peptide fragments (neopeptides) present in aged tendons,

178 Application of the active peptide fragment NT8-13 produced synaptic depression tha

179 gen-associated molecular patterns, including peptide fragment of bacterial flagellin (flg22) or trans

180 It was shown that a 45-mer peptide fragment of collagen type II with five hydroxypr

181 Using in vitro systems, we have identified a peptide fragment of gankyrin, 176LHLACDEERN185, which is

182 Previously, we have identified a small peptide fragment of IL-2 that was found to contain the e

183 reatment of MeCP2 mutant mice with an active peptide fragment of Insulin-like Growth Factor 1 (IGF-1)

184 as reinhardtii centrin for calcium and for a peptide fragment of Kar1p using CD, fluorescence, and NM

185 that the binding mode and stoichiometry of a peptide fragment of NDR (NDR(62-87)) is the same as for

186 location of PPAR-gamma is blocked by a short peptide fragment of NOC that inhibits its physical inter

187 bound to a 15 amino acid residue N-terminal peptide fragment of p85.

188 PAP(248-286) is a peptide fragment of prostatic acid phosphatase and has b

189 I), an amyloid fibril formed from a cationic peptide fragment of prostatic acidic phosphatase (PAP),

190 Adult SJL mice injected i.p. with a peptide fragment of proteolipid protein (a candidate aut

191 One peptide fragment of semenogelin I, termed SG-1, was puri

192 we report the high-resolution structure of a peptide fragment of the amyloidogenic protein transthyre

193 Introduction of the C-terminal peptide fragment of the ArPIKfyve-ArPIKfyve contact site

194 Dialysis of a small peptide fragment of the auxiliary beta4 Na(+) channel su

195 The peptide fragment of the channel is based on a conserved

196 f cancer marker protein Ki67 (Ki67FHA) and a peptide fragment of the hNIFK signaling protein.

197 This study indicates that a small peptide fragment of the human PEDF molecule could be eng

198 A peptide fragment of the I-II loop was purified from bact

199 assessed whether administration of a soluble peptide fragment of the NgR (sNgR) that binds to and blo

200 myloid fibrils formed from a self-assembling peptide fragment of the protein prostatic acid phosphata

201 A recombinant peptide fragment of the SMRT (silencing mediator for ret

202 NMR studies showed that a peptide fragment of the V2R C terminus containing the RG

203 d VEGF-A binding in the NRP1 b1 domain and a peptide fragment of VEGF-A was shown to bind at the same

204 haracterize separation between amyloidogenic peptide fragments of alpha-synuclein.

205 of DCs to internalize, degrade, and express peptide fragments of antigenic proteins on their surface

206 s were substantially inhibited by N-terminal peptide fragments of Anxa2 or anti-Anxa2 antibodies.

207 CD8(+) T cells recognize peptide fragments of endogenously synthesized antigens o

208 uence curvature sensing and explores whether peptide fragments of even shorter length can function as

209 ss spectrometric analysis of the proteolytic peptide fragments of IN.

210 tagonists of NgR derived from amino-terminal peptide fragments of Nogo-66.

211 roups by those measured by Kuhlman et al. in peptide fragments of NTL9.

212 pansion, followed by exposure to overlapping peptide fragments of PE38 and an IL-2 ELISpot assay to m

213 cyte Antigen (HLA) Class I molecules bind to peptide fragments of proteins degraded inside the cell a

214 ificant reactions of the monochloramine with peptide fragments of proteins that are associated with c

215 gators have therefore preferred to work with peptide fragments of PrP, suggesting that these peptides

216 ficity of otherwise poorly active N-terminal peptide fragments of PTH by conjugating them to nanobodi

217 betic (NOD) mice, repeated administration of peptide fragments of target antigens in incomplete Freun

218 ionization mass spectrometry identified two peptide fragments of the alphaB crystallin Walker-B moti

219 posits of insoluble, fibrillar aggregates of peptide fragments of the amyloid precursor protein (APP)

220 state: the protein in 6 M urea, and unfolded peptide fragments of the protein in water.

221 Previous studies have shown that synthetic peptide fragments of the PrP sequence corresponding to r

222 The tryptic peptide fragments of this phosphoprotein were sequenced

223 Importantly, expression of recombinant peptide fragments of wild-type SOD1 in cultured cells al

224 the modified ubiquitin and isomeric glycated peptides (fragments of bovine serum albumin (BSA)).

225 on, expression of a dominant negative mutant peptide fragment or injection of a function-blocking ant

226 allows the controlled production of typical peptide fragments or elemental reporter ions informing a

227 gamma-chains of fibrin and the appearance of peptide fragments over time were assessed by polyacrylam

228 he CD8(+) T-cell surface interact with short peptide fragments (p) bound to MHC class I molecules (pM

229 In addition, the peptide fragment PAMP(12-20) inhibits tumor cell-induced

230 Recently, a peptide fragment (PAP(248-286)) has been isolated from s

231 On uPA activation, NIR-NFP releases peptide fragments (PEG(54)-BK(NIR664)SGR-CONH(2)) that c

232 Full-length and conserved C-terminal delta peptide fragments permeabilize the plasma membranes of n

233 olyglutamine-expanded huntingtin protein and peptide fragments (polyQ-Htt).

234 CTLs recognize short peptide fragments presented in association with MHC clas

235 udy, we provide evidence that the C-terminal peptide fragment produced by caspase cleavage inhibits t

236 Low molecular weight protamine (LMWP) is a peptide fragment produced in our laboratory from enzymat

237 These results indicate that urinary peptide fragments reflect changes in expression of intac

238 scopic and mass spectrometric studies of the peptide fragments resulting from tryptic digestion of Ka

239 nce liquid chromatographic separation of the peptide fragments resulting from tryptic digestion of re

240 and structure of microbial communities using peptide fragment sequences extracted from metagenomic se

241 Both VGF and pro-SAAS are cleaved into peptide fragments, several of which are biologically act

242 em, it is generally assumed that angiotensin peptide fragments shorter than angiotensins II and III,

243 ts on the full alphatalpha motif and its two peptide fragments show that interhelical tertiary contac

244 ons followed by MALDI-TOF MS analysis of the peptide fragments showed these 47 kDa species to be CRP

245 A serine-rich peptide fragment spanning residues 221 to 240 was highly

246 e species include full-length SOD1 proteins, peptide fragments, stable oligomers and ubiquitinated en

247 ) NMR study of the fibrils formed by a small peptide fragment, structural details of beta(2)m fibrils

248 tive did not identify any covalently labeled peptide fragments, suggesting that the phenylazido side

249 ansfected HEK-293 cells revealed that a CFTR peptide fragment that binds AMPK (CFTR-1420-57) disrupte

250 an be used as a template to design a minimal peptide fragment that can be used as a drug against Rho-

251 A crystal structure, solved using a peptide fragment that contained residues 12 to 60, depic

252 e the solution structure of the Abeta(21-30) peptide fragment that may be relevant for understanding

253 A peptide fragment that spans the IQ motif of p68 strongly

254 otease digestion of the complex, generated a peptide fragment that was bound to the SG promoter.

255 ty of SagA is required and generates muramyl-peptide fragments that are sufficient to protect C. eleg

256 oach involves the digestion of proteins into peptide fragments that can be detected and sequenced wit

257 radation, inflammation and invasion liberate peptide fragments that can subsequently interact with ce

258 th or without CKI-alpha depletion identified peptide fragments that corresponded to the region locate

259 osurvival signaling or generate proapoptotic peptide fragments that help to execute the death program

260 Consistent with this model, peptide fragments that included the membrane binding reg

261 arboxyl-terminal parathyroid hormone (C-PTH) peptide fragments that may be present at only picomolar

262 acquisition of approximately 100 overlapping peptide fragments that redundantly cover the 243-residue

263 that barnase can be split into two inactive peptide fragments, that when co-expressed can complement

264 the C-terminal acyl donor and using smaller peptide fragments, the Cys(29)-Gly(77) glycopeptide doma

265 derived from automatic Edman degradation of peptide fragments, the SmCI sequence was fully character

266 Alanine ligation was used to assemble four peptide fragments, themselves prepared by solid phase pe

267 The heme-peptide fragment then oxidized 2,2'-azino-bis(3-ethylben

268 are generally characterized through tryptic peptide fragments, this paper reports a method for the i

269 ies via the deactivation of the SrtA-excised peptide fragment through diketopiperazine (DKP) formatio

270 ble to effectively stabilize the problematic peptide fragment through the attachment of cleavable arg

271 omochiral products from a racemic mixture of peptide fragments through a chiroselective autocatalytic

272 acyl-enzyme intermediate linking one of the peptide fragment to a catalytic subunit of the proteasom

273 MyBP-C (cMyBP-C), we added human N-terminal peptide fragments to human and rodent skinned ventricula

274 A peptide fragment, UQ(1-51), encompassing residues 1 to 5

275 ex with the human receptor and a coactivator peptide fragment using x-ray crystallography at 1.9-A re

276 However, the challenging exchange of peptide fragments using a dynamic covalent peptide bond

277 d 168 h and the supernatant was screened for peptide fragments using Tandem Mass Spectrometry.

278 A major peptide fragment was detected at m/z 1088 by a MALDI-TOF

279 increase in the relative intensities of the peptide fragments was achieved, which led to the identif

280 ity relationship of human LL-37, a series of peptide fragments was designed.

281 aterial throughput and convergency, the five peptide fragments were assembled into the native ATAD2 b

282 ch protein digest and the number of detected peptide fragments were compared with conventional MALDI

283 the peptide bonds of BSA were hydrolyzed and peptide fragments were desorbed from the surface of gold

284 The same peptide fragments were formed when the lead peptide was

285 Three distinct p21 derived peptide fragments were found to bind to DAPK; however, t

286 ll-length Gag-p24 protein, and the resulting peptide fragments were identified by mass spectrometry.

287 ng MALDI-TOF MS, and 102 out of 153 possible peptide fragments were identified giving a sequence cove

288 digested with chymotrypsin, and the modified peptide fragments were isolated and characterized as 6-h

289 C-PTH peptide fragments were isolated from plasma samples by i

290 ed caspase-3 in vitro, 13- and 17-kDa capsid peptide fragments were observed and were predicted by al

291 th trypsin and endoproteinase Asp-N, and the peptide fragments were purified by high performance liqu

292 le GFAP- and MBP-immunoreactive proteins and peptide fragments were seen, and many of them were also

293 Nonglycosylated peptide fragments were susceptible to complete Pronase d

294 istinct proteasomal degradation patterns and peptide fragments were unique to either mature DC or act

295 A longer peptide fragment which contains the first and second hel

296 ) is a naturally occurring 40- or 42-residue peptide fragment with a primary role in Alzheimer's dise

297 B), specifically and rapidly hydrolyzes stem peptide fragments with a free N-terminus.

298 omic sequence collections revealed groups of peptide fragments with a relatively high abundance and n

299 N-terminally formylated signal peptide fragments with variable sequence and length acti

300 driven dissociation because glycan-retaining peptide fragments would not be required for localization