ライフサイエンスコーパス: peptide

1 d essential interactions with the GAP5040-48 peptide.

2 ncodes a nodule-specific cysteine-rich (NCR) peptide.

3 diverse array of targets, including a short peptide.

4 tions in the oligomerization of IAPP-derived peptides.

5 nnate immune responses to undigested gliadin peptides.

6 k for developing effective fusion inhibitory peptides.

7 ionships of 76 different Abeta40 and Abeta42 peptides.

8 city filter that prevents binding of non-NES peptides.

9 h interday CVs < 20% for 80% of the glycated peptides.

10 d the resulting fibrils are composed of both peptides.

11 e specifically targeted by fusion-inhibitory peptides.

12 the presence of H3K36me3-containing histone peptides.

13 red relative changes of denaturation between peptides.

14 a variety of complexes with short synthetic peptides.

15 ion and packing can adapt to the presence of peptides.

16 , and the presence of cationic antimicrobial peptides.

17 and on the expression of ileal antimicrobial peptides.

18 x with the HLA-E molecule presenting the two peptides.

19 secrete some of the Drosophila insulin-like peptides.

20 inhibitory polypeptide (GIP), glucagon-like peptide 1 (GLP-1), and peptide tyrosine tyrosine (PYY)]

21 Here, we present evidence for glucagon-like peptide 1 (GLP-1)-mediated paraventricular hypothalamic

22 is method using dulaglutide, a glucagon-like peptide 1 (GLP1)-Fc fusion protein.

23 to controllably release GLP-1 (glucagon-like peptide 1), a critical incretin that regulates blood glu

24 Exendin-4 (EX-4), a glucagon-like peptide-1 (GLP-1) receptor agonist, has been shown to re

25 ting analog of the gut-hormone glucagon-like peptide-1 highlights the therapeutic potential of gut-de

26 The glucagon-like peptide-1 receptor (GLP-1R) and the glucagon receptor (G

27 pal neurons to reduce (leptin, glucagon-like peptide-1) or increase (ghrelin) food intake and learned

28 The aggregation of the amyloid beta peptide (Abeta) into amyloid fibrils is a defining chara

29 platform as a quantitative screen to assess peptide activity and selectivity by precisely controllin

30 patients with altered urinary antimicrobial peptide activity developed either an E. faecalis or Pseu

31 atorial reflections, suggesting that the two peptides adopt distinct lateral packing of the diffracti

32 pothalamic neurons expressing agouti-related peptide (AgRP) and neuropeptide Y (Npy).

33 t ArcN NPY neurons expressing agouti-related peptide (AgRP) in mice, we have demonstrated that this n

34 'hunger neurons' (expressing agouti-related peptide (AgRP)) bypasses these signals to restore hunger

35 S. aureus uses secreted cyclic autoinducing peptides (AIPs) and the accessory gene regulator (agr) o

36 Application to peptides allowed expedient preparations of alpha-amino b

37 autophagy using a specific inducer Beclin-1 peptide ameliorates cysts in the pkd1a model.

38 f STP-C1 using UPLC-MS/MS identified sixteen peptides/amino acids.

39 on a supramolecular liquid crystal formed by peptide amphiphiles (PAs) that encapsulates cells and gr

40 controlled by simply modulating the starting peptide and fluorinated solvent concentrations during sy

41 SCENCE DEFICIENT IN ABSCISSION (IDA)-derived peptide and its receptors, HAESA (HAE) and HAESA-LIKE2 (

42 n analysis of TCR sequences using a panel of peptide and major histocompatibility complex (pMHC)-tetr

43 is melo) eIF4E in complex with a melon eIF4G peptide and propose the first eIF4E-eIF4G structural mod

44 copy has been previously used to investigate peptide and protein binding to lipid membranes, as it al

45 stability of an arginine-containing collagen peptide and provide a structural basis for this stabiliz

46 McpM has four cysteines within the mature peptide and site-directed mutagenesis experiments demons

47 the MNs, the intrinsic hydrophobicity of the peptide and the species of skin model used in laboratory

48 e reported for the detected peptide queries, peptides and inferred proteins.

49 hR complex, and is extendable to other toxin peptides and ion channels.

50 cepted by amine reactants to generate amides/peptides and o-mercaptobenzamides.

51 er anticancer agents and nanoparticles using peptides and other affinity ligands may represent a gene

52 MaxQuant was used to identify peptides and proteins and quantify heavy/light lysine ra

53 thermal decomposition reactions that cleave peptides and proteins specifically at the C-terminus of

54 ional ensembles for intrinsically disordered peptides and proteins.

55 bonds between C-terminal residues of lentil peptides and residues of the ACE catalytic site.

56 ted structural analogy with cell-penetrating peptides and that both the entire protein and the peptid

57 acid arginine at the second position of the peptide, and hydrophobic and polar amino acids at the C-

58 The resource will be extended to >1 million peptides, and all data will be shared with the community

59 oth classic characteristics of antimicrobial peptides, and we observed that IFN-beta can directly kil

60 formans polysaccharide capsule, hydrolyzed a peptide antigen mimetic.

61 lobulin-like variable domains that recognize peptide antigens associated with major histocompatibilit

62 d graphene oxide (GO) sheets with a specific peptide aptamer to create a novel, simple and label-free

63 Our data suggest that NCR peptides are host determinants of symbiotic specificity

64 ity, and challenge the view that stimulatory peptides are the ultimate gatekeepers of puberty.

65 obably a helix barrel that contains eight D4 peptides arranged in parallel.

66 f commutability of tryptic and cleavable SIL peptides as internal calibrators across various bottom-u

67 All peptides, as well as full length Sap6, demonstrated amyl

68 ntibacterial materials by integration of the peptide assemblies into tissue scaffolds.

69 sion of myosin heavy chain 7 and natriuretic peptide B is up-regulated in both ventricles with right

70 We conclude that involvement of the peptide backbone's carbonyl and amide groups in hydrogen

71 the conformational space available to simple peptide-based catalysts is more diverse than precedent m

72 aper describes the development of a class of peptide-based inhibitors as novel antitrypanosomal and a

73 roteolytic digestion of unbound proteins and peptide-based phosphorylation enrichment.

74 alities at an early stage of pregnancy, a GO-peptide-based surface plasmon resonance (SPR) biosensor.

75 t-parenting solitary adults and quantify 133 peptides belonging to 18 neuropeptides.

76 to a structure similar to other sea anemone peptides belonging to structural group 9a.

77 ating turns, which are highly reminiscent of peptide beta-turns.

78 d variant located at position 71, within the peptide-binding groove of HLA-DRB1 (P = 2 x 10(-4) ).

79 Circulating RBP4, TTR, B-type natriuretic peptide (BNP), and troponin I (TnI) concentrations and e

80 the preparation of the labeled antimicrobial peptide BODIPY-cPAF26 by solid-phase synthesis (6-7 d) a

81 g of their CCA-ends into the PTC thus making peptide bond formation impossible.

82 The resulting monomeric peptide (brHis2) does not bind to its consensus target D

83 ial library made from a threonine containing peptide building block, which, by itself, only forms tri

84 rediction of human leukocyte antigen-binding peptides by in silico algorithms, but the predictive pow

85 d due to rapid proteolysis of apelin-derived peptides by proteases, including neprilysin (NEP).

86 As a consequence, a single peptide can act through several mechanisms depending on

87 Calcitonin gene-related peptide (CGRP) stimulated CLR endocytosis and activated

88 led antibody against calcitonin gene-related peptide (CGRP), a marker of nociceptive sensory nerves.

89 l polypeptide (VIP), calcitonin-gene related peptide (CGRP), substance P (SP), neuropeptide tyrosine

90 spond to CO2 express calcitonin gene-related peptide (CGRP), we hypothesized that CGRP may provide a

91 and substrate preference using a fluorogenic peptide cleavage assay.

92 e mechanism by which co-translational signal-peptide cleavage is prevented.

93 but that a phosphorylated central C-terminal peptide competed for association with beta-arrestin 1, a

94 phosphorylated central or distal C-terminal peptides competed for association with beta-arrestin 2.

95 monstrated that central or distal C-terminal peptides competed for the CB1R association with CRIP1a,

96 By utilizing the biomineralizing peptide component displayed on the bacteriophage surface

97 her median N-terminal pro-B-type natriuretic peptide concentration (403 versus 320 pg/mL; all P<0.01)

98 The incremental area under the plasma C-peptide concentration curve during the hyperglycemic cla

99 nt the synthesis and characterization of new peptide conjugates obtained by hierarchical co-assembly

100 However, the peptide containing the selected motif, LRLLRWC, was not

101 iques to separate and sequence de novo proto-peptides containing broader combinations of prebioticall

102 he majority of studies in the field focus on peptides containing only one or two types of amino acids

103 Cyclic peptides containing the Arg-Gly-Asp (RGD) sequence have

104 Consistent with this, a synthetic peptide corresponding to the HAP2 fusion loop was found

105 of Plasmodium falciparum 3D7 parasites with peptide corresponding to the hemoglobin binding domain i

106 des and that both the entire protein and the peptide corresponding to the N-terminal moiety of MF6p/F

107 ed from the ketoacids in the presence of the peptide coupling reagent HATU and NHC generated from the

108 Although cationic cell-penetrating peptides (CPPs) are able to bind to cell membranes, thus

109 It is a 35-amino acid peptide cross-linked by two disulfide bridges named tau-

110 nal linker (CTL), and a C-terminal conserved peptide (CTC).

111 Various chloroplast transit peptides (CTP) have been used to successfully target som

112 Polytheonamides are potent peptide cytotoxins produced by uncultivated bacteria tha

113 centrations in vivo, d-amino acid containing peptides (DAACPs) are crucial to many life processes.

114 mechanical circulatory support, natriuretic peptide decile, glomerular filtration rate, and total bi

115 Thus, we demonstrated peptide-dependent binding of the activating NK cell rece

116 e reversible immobilization of amino acid or peptide derivatives on carbon nanomaterials such as [60]

117 the binding site, we used a series of decoy peptides derived from the primary amino acid sequence in

118 -0.28) in inferring proteins without need of peptide detectability on which the most competitive meth

119 he chromatographic peak picking accuracy and peptide detection capability of PECAN, and we further va

120 sing of soluble and cell-associated Ags into peptide displayed by MHC I is however defective in hepat

121 the production of multi-functional bioactive peptides due to the hydrolysis of whey proteins.

122 in the conformational preferences of a model peptide during the transition from a hydrated environmen

123 etric sequence-specific model for predicting peptide electrophoretic mobility has been developed usin

124 asma from cancer patients and discovered two peptides encoded by the peptidyl-prolyl cis-trans isomer

125 ted by the antagonistic activities of both a peptide-encoded N-terminal nuclear localization signal a

126 rmined a crystal structure of CaM bound to a peptide encompassing its binding site in AKAP79.

127 responses and neutralization than the native peptide epitope.

128 ive in autoproteolysis and hence, in Stachel peptide exposure.

129 ds and highlight connections between protein/peptide folding, unfolding and aggregation mechanisms, w

130 ed hydroxides could have played in prebiotic peptide formation.

131 The exact location of the CoV fusion peptide (FP) has been disputed.

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

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

134 s responding weakly to hundreds of MHC-bound peptides from graft-derived leukocytes.

135 edicted HLA class I- and class II-restricted peptides from rDEN2Delta30 and used them in a gamma inte

136 ments on lipid association of the C-terminal peptide fully recapitulated their effects on the subcell

137 study showed that treatment with the Kalpha2 peptide fused with the TAT peptide significantly inhibit

138 The recently developed peptide GL13K is used as an example to illustrate many o

139 wed similar reductions in insulin, insulin C-peptide, glycated hemoglobin, and homeostasis model asse

140 The peptide, gold nanoparticle and aminosilane solution was

141 The concept of natriuretic peptide guidance has been extensively studied in patient

142 The limitations of peptides have severely hampered their use in pharmacolog

143 The peptide hormone calcitonin is intimately connected with

144 The peptide hormone human relaxin-2 (H2-RLX) has emerged as

145 en the importance of insulin and its related peptide hormones and previous studies of glycosylated in

146 Neuropeptides are peptide hormones used as chemical signals by the neuroen

147 a rich source of bioactive molecules such as peptides, hormones, and neurotransmitters, but relativel

148 xtraction due to accumulation of hydrophobic peptides (IC50 between 12 and 21mg/l).

149 improve reproducibility, peak capacity, and peptide identifications to rival modern hybrid quadrupol

150 om two T1D subjects recognized distinct IGRP peptides, implicating this molecule as a trigger for CD4

151 rgeting of p32 with linTT1 tumor-penetrating peptide improves tumor selectivity and antitumor efficac

152 This study suggests applications for UNO peptide in diagnostic imaging and therapeutic targeting

153 captivus in the presence of an antimicrobial peptide in vitro, inactivation of both phoP and Sant_406

154 which are easily multiplexed to target many peptides in a single assay.

155 ed proteolysis is known to produce antigenic peptides in adaptive immunity, our findings demonstrate

156 ch determines sequence-dependent behavior of peptides in HILIC.

157 suggesting a role for urinary antimicrobial peptides in susceptibility to select uropathogens.

158 Conventional peptides in the 20-40-mer length range are rapidly degra

159 enrichment efficiency with 85% of identified peptides in the enriched fraction as glycated, high sens

160 lutamic acid and glutamine, and further with peptides, in A. thaliana cells.

161 These peptides induce autophagy at micromolar concentrations i

162 sing this approach, an optimized macrocyclic peptide inhibitor (HL2-m5) was obtained that binds Shh w

163 A selective peptide inhibitor of AMPH-dependent trafficking of the n

164 the effect of RA101295, a 2-kDa macrocyclic peptide inhibitor of C5 cleavage, using in vitro whole-b

165 Using selective peptide inhibitors of the CXCL1-CXCR2 signaling axis ide

166 eres with the deep insertion of a Tat signal peptide into the TatBC receptor complex.

167 eptides, such as the well-known amyloid-beta peptide involved in Alzheimer's disease.

168 electrospray ionization) to the solvent-free peptide ion.

169 A large number of bioactive peptides isolated from natural sources are known to play

170 sing gamma-MSH as a template, we developed a peptide, [Leu(3), Leu(7), Phe(8)]-gamma-MSH-NH2 (compoun

171 g protein, troponin T, and brain natriuretic peptide levels were measured.

172 fe, higher N-terminal pro-B-type natriuretic peptide levels, and a poorer prognosis.

173 lin 2) and are accompanied by elevated Abeta peptide levels.

174 pite lower N-terminal pro-B-type natriuretic peptide levels.

175 d viremic KTR were stimulated using BK virus peptide libraries loaded or not on monocytes-derived den

176 e previously been delineated using synthetic peptide libraries of fixed length, or single protein cha

177 uration through the screening of macrocyclic peptide libraries produced in E. coli cells.

178 was used to isolate mimotopes from a 12-mer peptide library in successive selection rounds.

179 release is controlled by the sequence of the peptide linker.

180 ms depending on the peptide's structure, the peptide:lipid ratio, and the properties of the lipid mem

181 ted based on responses to HIV-1-infected and peptide-loaded target cells.

182 cell-mediated immunity is the recognition of peptide-major histocompatibility complex class I (p-MHC

183 MAM is a peptide mapping method utilizing mass spectrometry to de

184 The most robust tryptic peptide marker in the validation was LTLGSALAAPQR.

185 s for which heat-stable and species-specific peptide markers had been detected.

186 at oxidation and elevated atrial natriuretic peptide message of cardiac hypertrophy.

187 five major CM proteins were measured with a peptide microarray-based immunoassay.

188 14-3-3 protein complexes by small molecules, peptide mimetics, and natural products.

189 erate the cleavage of the magnetic nanobeads-peptide moieties away from the sensor surface upon test

190 HCA1 interaction with both the N-glycan and peptide-moiety of SV2.

191 racts with alphabeta-tubulin through a small peptide motif within its MT-binding domain.

192 ological approaches, including use of either peptide:N-glycosidases F and A (PNGase F and A) or anhyd

193 d higher levels of binding affinity with NHR peptide N46.

194 and functionally characterized one of these peptides named "avathrin." Avathrin is a fast, tight bin

195 dified to produce a panoply of antimicrobial peptides now known.

196 The cardiac natriuretic peptides (NPs), atrial NP and B-type NP, regulate fluid

197 al care on N-terminal pro-B-type natriuretic peptide (NT-proBNP) levels compared with usual care alon

198 based on the strand replacement of dsDNA by peptide nucleic acid (PNA) and the in situ growth of ele

199 rrelating with gene knockdown, we employed a peptide-nucleic acid (PNA) hybridization assay.

200 For example, the Stachel-derived peptide of GPR110 (subfamily VI) can activate GPR64 and

201 We combine a 97-amino-acid peptide of human origin that binds hyaluronan, a major m

202 ds to both the closed conformation and the N-peptide of Syx4.

203 spectrometry to detect and quantify specific peptides of interest.

204 itative detection of model amphipathic viral peptide on a screen-printed electrode.

205 approach, we successfully incorporate (D)CDX peptides onto the surface of RBCNPs without compromising

206 The peptide orientation, as determined by NMR, showed that t

207 g many neuropeptides, including hypothalamic peptide orthologs and their receptors.

208 Targeted mass spectrometry of a surrogate peptide panel is a powerful method to study the dynamics

209 (CatS) and the intramembrane protease signal peptide peptidase-like 2a (SPPL2a).

210 ODZ1 through proteolytic cleavage by signal peptide peptidase-like 2a.

211 ing electron microscopy, we showed that this peptide physically destroyed influenza virions.

212 ast MDA-MB-231 tumors showed that the cyclic peptide preferentially accumulates in tumor (2 h after i

213 Endogenous myelin peptide presentation to CD4(+) T cells following phagocy

214 They recognize defective cells by binding to peptides presented on the cell surface by MHC class I mo

215 antigens, which are tumour-specific, mutated peptides presented on the surface of cancer cells.

216 wing that the N-terminal acidic region of Ng peptide pries open the beta-sheet structure between the

217 DP(84Gly) constitutively presents endogenous peptides processed by the proteasome and transported to

218 f innate IL-17, which promotes antimicrobial peptide production, whereas pathogen-specific Vgamma4 ce

219 criteria should be reported for the detected peptide queries, peptides and inferred proteins.

220 interaction with relaxin/insulin-like family peptide receptor 2 (RXFP2).

221 55 proteins contained the lipoprotein signal peptide recognition site of signal peptidase II (SpII).

222 timized to obtain efficient and reproducible peptide recovery in only 30 min.

223 ions, N-terminal methionine excision, signal peptide removal, and some post-translational modificatio

224 , we analyzed the individual responses of 38 peptides reporting for 25 proteins of interest in 170 or

225 Localization is routinely limited to a peptide resolution of 5 to 20 amino acid residues.

226 es showed that 52% and 48% of the identified peptides, respectively, were affected by PTMs, with a to

227 days, respectively (P < 0.01); the plasma C-peptide response remained unchanged in subjects with NFG

228 Position-dependent effects on peptide retention for different residues were driven by

229 Immunohistochemistry using a biotin-modified peptide (RK-10-Biotin) was tested against the FDA-approv

230 of virulence in P. aeruginosa by a designed peptide (RpoN molecular roadblock, RpoN*) which binds sp

231 e surface of RBCNPs without compromising the peptide's brain targeting ability.

232 through several mechanisms depending on the peptide's structure, the peptide:lipid ratio, and the pr

233 We find low peptide-S/N concordance between arrays, demonstrating th

234 individual characterization and that global peptide-S/N relationships are difficult to identify.

235 R(2) approximately 0.995) indicates that the peptide separation process in CZE is relatively simple a

236 processing was performed to obtain confident peptide sequence assignments, allowing the detection of

237 Binary encoding of peptide sequences into differential antimicrobial mechan

238 Using rationally designed short peptide sequences, we determined that the charge type an

239 the all-atom MD simulations for Abeta(14-23) peptide shows that surface interactions induce conformat

240 with the Kalpha2 peptide fused with the TAT peptide significantly inhibited IAV replication and tran

241 The same peptides significantly altered a nicotinic receptor indu

242 pH positively affected peptides, soluble phenolic compounds and antioxidant act

243 ation and study its effects on generation of peptides, soluble phenolics and bioactivities.

244 frequency of these residues generates short peptides, some of which are too small or uninformative f

245 ), CA carries a short and hydrophobic spacer peptide (SP) at its C-terminus early in the maturation p

246 cture of the C-terminal region of CA and the peptide SP1 (CA-SP1), which represents an intermediate d

247 oduced synthetic vaccines that induce strong peptide-specific CD8(+) T cell responses in vivo by inco

248 predicted to bind these self- and microbial peptides strongly, and these responses were more common

249 lutionary interplay between the prochlorosin peptide substrates and the lanthionine synthetase sugges

250 ed activity toward hydroxyproline-containing peptide substrates.

251 Such biomolecules include amyloidogenic peptides, such as the well-known amyloid-beta peptide in

252 etry assays for protein quantitation monitor peptide surrogates, which are easily multiplexed to targ

253 n of nanoparticles with the cell-penetrating peptide TAT increases their biophysical association with

254 The resulting peptide (TAT-C1aB) suppressed enhanced whole-cell K(+) c

255 out a detailed characterization of the Esrp1 peptide that is sufficient to confer nuclear localizatio

256 Moreover, use of a triple-helical peptide that reconstitutes the collagen-binding domain f

257 By combining an alpha-helical peptide that self-assembles into a hexameric coiled-coil

258 Here we construct simple peptides that assemble into well-defined amyloid phases

259 Hydrocarbon-stapled peptides that display key residues of the p53 transactiv

260 Nexvax2 is an adjuvant-free mix of three peptides that include immunodominant epitopes for gluten

261 Here, we identified a series of peptides that interact specifically with the DNA binding

262 idence for two populations of PmB molecules: peptides that lie flat on the membranes, and an inserted

263 ected mutagenesis and by inhibition by small peptides that mimic the loop residues.

264 bust autophagy activity of the Kalpha2-helix peptide, the present study showed that treatment with th

265 NT-proBNP (N-terminal pro-B-type natriuretic peptide), TNF-alpha, IL-6, IL-12, IL-17, malondialdehyde

266 or AD by directly interacting with the Abeta peptide to inhibit Abeta42 fiber formation.

267 brates by binding and presenting immunogenic peptides to cytotoxic T lymphocytes.

268 des mobile EPIDERMAL PATTERNING FACTOR (EPF) peptides to enforce stomatal spacing.

269 ncreased IL-1beta boosts local antimicrobial peptides to facilitate microbiota remodelling.

270 undamental challenges of docking large toxin peptides to ion channel homology models, as exemplified

271 s consistently capturing and presenting more peptides to Tfh cells than other lineages of more specif

272 channels and a binding protein in which the peptide toxins successfully reverted back to near-native

273 Venom peptide toxins such as conotoxins play a critical role i

274 ng algorithm was highlighted by redocking of peptide toxins to two ion channels and a binding protein

275 Several motif variant peptides translocate into synthetic vesicles with rates

276 (GIP), glucagon-like peptide 1 (GLP-1), and peptide tyrosine tyrosine (PYY)] were measured, and ad l

277 Peptides undergo changes in conformation and aggregation

278 driven by the spatial orientation of tryptic peptides upon interaction with the negatively charged su

279 say, and antibodies to a deamidated gliadine peptide using an immunofluorometry assay.

280 for identifying target-binding cystine-dense peptides using mammalian surface display, capable of int

281 onjugating the chlorin to a cell penetrating peptide, using bioorthogonal ligation chemistry.

282 igate the presence and colocalization of the peptides vasoactive intestinal polypeptide (VIP), calcit

283 g of MKK2 protein and its T31 phosphorylated peptide verified the phosphoproteomic results of increas

284 The most active peptide was completely symmetrical, rich in Arg and Trp

285 dress this gap, a genetically encoded cyclic peptide was designed based on the sonic hedgehog (Shh)-b

286 reus that is more sensitive to antimicrobial peptides was killed more efficiently by IFN-beta than wa

287 receptor-blocking antibodies and activation peptides, we determined that thrombin-mediated injury de

288 All peptides were collagen fragments, suggesting that these

289 These peptides were extended at the C terminus (POmega) and co

290 NT-proBNP (N-Terminal Pro-B-Type Natriuretic Peptide) were retained (chi(2), 62.2; P<0.0001).

291 hen investigated whether the p75(alphagamma) peptide, which is a product of both alpha- and gamma-cle

292 Ubiquicidin is an antimicrobial peptide with great potential for nuclear imaging of infe

293 12f is a new structural class of amphiphilic peptide with rapid fungicidal activity caused by C. neof

294 By first reacting a bifunctionalized peptide with the more specific KalbTG and in a second st

295 Several peptides with DPP-IV inhibitory features or known activi

296 , high sensitivity for detection of glycated peptides with LOD and LOQ at 1.2 and 2.4 pg, respectivel

297 ine Xaa-Pro aminopeptidases, which hydrolyze peptides with proline at the second position (P1').

298 on of nanoparticles directly from functional peptides would therefore offer a versatile and robust pl

299 To compare the circulating plasma levels of peptide YY and ghrelin in control subjects and in critic

300 pathophysiologic role of the enterohormones peptide YY and ghrelin is supported by preclinical data.