ライフサイエンスコーパス: peptide

1 nhanced binding affinity compared to the p53 peptide.

2 and LMP7 by immunization with a cardiac TnI peptide.

3 e-based nanotransformer and loaded antigenic peptide.

4 tion and secondary nucleation of the Abeta42 peptide.

5 t regulatory sites: Na(+) and the inhibitory peptide.

6 try for strong binders than for low-affinity peptides.

7 A-A, -B, and -C genotypes for all SARS-CoV-2 peptides.

8 rease the prediction accuracy of immunogenic peptides.

9 occur, releasing large numbers of endogenous peptides.

10 is the delineation of the role of individual peptides.

11 omplex class I (MHC I) molecules loaded with peptides.

12 dentification of the first endogenous opioid peptides.

13 o see no increase in GSIS in response to CCK peptides.

14 was performed to identify motifs of binding peptides.

15 fication/quantification of partially labeled peptides.

16 ions (PTMs) affecting single amino acids and peptides.

17 ernal standards to quantify chosen surrogate peptides.

18 of ultra-low concentrations of the Abeta-40 peptides.

19 Exogenously provided competence stimulating peptide 1 (CSP1) failed to modulate the onset kinetics o

20 Glucagon-like peptide 1 (GLP-1) mimetics are effective drugs for treat

21 Glucagon-like peptide 1 receptor (GLP-1R) agonists effectively improve

22 Glucagon-like peptide 1 receptor (GLP-1R) imaging with radiolabeled ex

23 d (NIR) fluorescence imaging of glucagonlike peptide 1 receptor (GLP-1R)-positive lesions, using the

24 OS in mediating microglial response to Abeta peptide 1-42 (Abeta(42)) stimulation in vitro, in aging-

25 iazolidinediones (glitazones), glucagon-like peptide-1 (GLP-1) receptor agonists and dipeptidyl pepti

26 ch is required for the release of the fusion peptide(11,12).

27 IGF-1 (recombinant human IGF-1)/BP3 (binding peptide 3) improves lung growth and prevents PH in two a

28 A large number of Cys peptides (412) were redox switched, representing central

29 Oligomers of the beta-amyloid peptide, Abeta, play a central role in the pathogenesis

30 rmal electrophysiology, improves glucose and peptide absorption, diminishes diarrhea and rescues post

31 id that can readily be incorporated into any peptide accessible by standard solid-phase methods.

32 ions following HCD fragmentation of labeled peptides acquired on Orbitrap platforms at a minimum of

33 ists of opioid receptors to infer endogenous peptide activity, and genetic knockout of opioid peptide

34 ferentiated monocytes loaded with protein or peptide Ag.

35 GPR56 peptide agonists have antidepressant-like effects and up

36 o proopiomelanocortin (POMC), agouti-related peptide (AgRP), melanin-concentrating-hormone (MCH) and

37 Hypothalamic agouti-related peptide (AgRP)-expressing neurons are acutely activated

38 The peptide also inhibits cervicovaginal HPV16 pseudovirus i

39 right properties, for example Antimicrobial peptides (AMPs), can disrupt this protective barrier by

40 d stimulated to release stored antimicrobial peptides (AMPs).

41 We synthesized the 12-mer peptide and found that it binds the scFv antibody with a

42 ect into solution from the N or C-termini of peptide and protein substrates.

43 t at baseline identifies associations with C-peptide and stratifies subjects for future severity of C

44 -presenting cells, which function to present peptides and activate CD4 T cells.

45 ers resistance to host-derived antimicrobial peptides and bile, respectively.

46 These peptides and macrocycles, along with the dimeric model o

47 t that the self-replicator consisted of both peptides and nucleic acid strands.

48 Amyloidogenic peptides and proteins aggregate into fibrillary structur

49 satile and selective method to functionalize peptides and proteins through free-radical-mediated dech

50 ter has been the main application of VCD for peptides and proteins, although this is now reinforced b

51 ind amyloid fibrils formed from many natural peptides and proteins.

52 IRMPD exploited in dissociation protocols of peptides and proteins.

53 The ability to generate large panels of peptides and subsequently large bodies of peptide-MHC-II

54 the potential interactions between different peptides and the main anthocyanins from eggplant peels.

55 localized and delocalized motions present in peptides and where they can be found in the electromagne

56 biomarkers (troponins and B-type natriuretic peptide) and cardiac dysfunction for 24-48 h after event

57 sglutaminase, IgA against deamidated gliadin peptide, and endomysial antibody (IgA).

58 Phox2b, substance P, calcitonin-gene related peptide, and the serotonin receptor 5-HT(3)R.

59 This is demonstrated for small molecules, peptides, and proteins up to 66 kDa on three commerciall

60 source is demonstrated using beta-blockers, peptides, and proteins.

61 the balanced synthesis of its main effector peptides Ang (angiotensin) II and Ang (1-7).

62 sal epitope in VP2N which could be used as a peptide antigen to detect FMDV-specific antibodies again

63 infant controls (P < .01), recognized the KD peptide antigen.

64 Cyclic peptides are reported to have antibacterial, antifungal,

65 NPs (natriuretic peptides) are cardiac-derived hormones that promote natr

66 n composed of several concatenated signature peptides as internal standard.

67 ely demonstrate the nature and extent of EPF peptides as non-cell autonomous local signals and provid

68 VZV glycoprotein B (gB) peptides assembled into fibrils and catalyzed amylin and

69 ospect of future biocompatible devices where peptide assemblies could complex with native and non-nat

70 rticles that displayed the same self-antigen peptide at comparable epitope densities.

71 a 4-hour mixed-meal tolerance test (4-hour C-peptide AUC) at week 52.

72 ryptamine receptor 1F, natriuretic precursor peptide B, and neuromedin B.

73 jor impediment for the design of sustainable peptide-based antibiotics that can be hydrolyzed by wast

74 to a family of 3-19 nM-affinity, alpha/beta-peptide-based binders to 14-3-3.

75 In many cases, these peptide-based catalysts have enabled novel multifunction

76 he abacavir analogues within the HLA-B*57:01 peptide binding groove.

77 ese two positions are component parts of the peptide-binding pocket 7 (P7) of the HLA-DR heterodimer,

78 tion for differences in peptide profiles and peptide bioactivities.

79 ns involved in bioluminescence, nonribosomal peptide biosynthesis, fatty acid activation, and beta-la

80 kine ligand (CCL) 8 and synthesized a 16-mer peptide (BK1.1) based on this interface region in evasin

81 O-glycosylations on a multiply glycosylated peptide by virtue of enumerating the dehydration scars i

82 rometry responses (signal-to-noise ratio) of peptides by more than 1 order of magnitude on average af

83 thus enabling extraction of high amounts of peptides by the new C18/PAN coating.

84 n both the B-chain (B16-27 and B22-C3) and C-peptide (C25-35).

85 N-oxidized using an aspartic acid containing peptide catalyst to afford stable, helically chiral prod

86 We discovered that 2 crustacean cardioactive peptide (CCAP)-expressing neurons in Drosophila adults r

87 opsis and Medicago CEP (C-TERMINALLY ENCODED PEPTIDE)-CEP RECEPTOR signalling controls RSA, the gravi

88 red, small-molecule, calcitonin gene-related peptide (CGRP) receptor antagonist under investigation f

89 he rare cognate amino acids into the growing peptide chain at a rate of ~20 aa/s.

90 A previously unreported subset of small peptide-coding transcripts was identified from these lnc

91 utes toward inhibition of MHC class I:beta2M:peptide complex formation.

92 cts) with HLA proteins that present the drug-peptide complex to T cells.

93 At high peptide concentrations in the membrane, the (19)F-(13)C

94 We find that the ensembles of bound peptide conformations generated by the programs MODELLER

95 sing a single somatostatin receptor-targeted peptide conjugate as a theranostic agent.

96 an exploratory experiment in mice, a VHH-PTH peptide conjugate showed biological activity, whereas th

97 nsformer-based vaccine, comprising a polymer-peptide conjugate-based nanotransformer and loaded antig

98 Ala(13), Nle(14)]Bn(6-14) (sBB2L) generating peptide conjugates with up to 80 boron atoms per molecul

99 is we uncover previously uncharacterized CIF peptides conserved among higher plants.

100 be an initial source of amyloid beta (Abeta) peptide-containing amyloid plaque development.

101 y internalized by U87MG (proportional to the peptide content and abrogated by anti-alpha(v)beta(3)) b

102 tail of keyhole limpet hemocyanin-conjugated peptides corresponding to the AipA, Asp14, and OmpA bind

103 and pathways expressing the stress-sensitive peptide corticotropin-releasing factor (CRF), which has

104 ether tolerizing immunotherapy with a single peptide could control diabetes driven by multiple Ags, w

105 tibodies directed at 58 (15-mer) overlapping peptides, covering the entire sequence of ovomucoid, in

106 Cell penetrating peptides (CPP) have the ability to rapidly internalize a

107 onolayers is conjugation to cell-penetrating peptides (CPPs); however, very little is known about the

108 platform yields high-quality MHC-II-binding peptide datasets that can be used to improve the accurac

109 miRNAs may be useful in predicting future C-peptide decline for improved subject stratification in c

110 linear) peptide-decorated nanoparticles was shown in 2D culture

111 nical HLA peptides, including an immunogenic peptide derived from an open reading frame downstream of

112 viously designed and synthesized macrocyclic peptides derived from Abeta(17-23) and Abeta(30-36) that

113 olute values were observed for the P2 and P3 peptides derived from alpha- and gamma-gliadins.

114 uggest that non-canonical tumor-specific HLA peptides derived from annotated non-coding regions could

115 to the resulting ensemble such that averaged peptide-deuteration levels, as predicted by an empirical

116 specific CD8+ T cells could be identified by peptide/dextramer staining.

117 cal activity, whereas the corresponding free peptide did not.

118 We propose the unconventional use of peptide discs made by phospholipids and amphipathic 18A

119 s delineate how drug HLA-B*57:01 binding and peptide display by antigen presenting cells relate to th

120 ng rates are always slower than that of MHCI-peptide dissociation.

121 panel of variants of the Car9 silica-binding peptide (DSARGFKKPGKR) fused to the C-terminus of superf

122 gen may better engage B cells and designed a peptide encompassing the extracellular domains (ECD) of

123 In male neurons, the ED peptide enhanced neuritogenesis in the presence of an an

124 w cytometry of the five most highly abundant peptides (EP1, -2, -3, -7 or EP9) showed strong binding

125 ilter in shaping the repertoire of presented peptide epitopes and the formation of a hierarchical imm

126 lico techniques, we demonstrate that the two peptides, even if applied individually, transform origin

127 e methods include directly administering the peptides ex vivo (i.e., to excised tissue) or in vivo (i

128 ivo and an enhanced response to weak agonist peptides ex vivo.

129 We find that the most potent pore-forming peptides exhibit strong interpeptide interactions, inclu

130 fferents, increasing calcitonin gene-related peptide expression and basal trigeminal nociception.

131 zyme-instructed self-assembly of a synthetic peptide for trafficking endogenous proteins, this work p

132 In this study, production of peptide fractions with different molecular weights (10,

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

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

135 The peptide-free state of these molecules is not well unders

136 deprotonation of Glu8 to release the hormone peptide from the amyloid.

137 Finally, producing antimicrobial/antioxidant peptide from wastes by EDUF fits perfectly with the conc

138 bit the release of puromycin-labeled nascent peptides from ribosomes.

139 solvents improves digestion, generating more peptides from the rigid beta-barrel regions, without com

140 s review aims to focus on recent advances in peptide-functionalized liposomal formulation techniques

141 iomarkers (N-terminal pro-B-type natriuretic peptide [>40 pg/mL] or troponin T [>0.6 pg/mL]) were rec

142 CANCE STATEMENT The neuropeptide VGF and its peptides have been associated with many metabolic and ne

143 Oxytocin-like peptides have been implicated in the regulation of a wid

144 Aggregation of the peptide hormone amylin into amyloid deposits is a pathol

145 This is exemplified by the plant-peptide hormone mimics, the CLAVATA3/EMBRYO SURROUNDING

146 rk for the recognition of sequence-divergent peptide hormones in plants.

147 Like many peptide hormones, OCN is subjected to post-translational

148 he various segments of the full-length hIAPP peptide; however, only a few have their origin from the

149 Ang (1-7) is the dominant RAS peptide in healthy human kidneys with NEP rather than AC

150 since no T cells recognizing any EBV-derived peptide in this common HLA allele have been found thus f

151 vity superior to that of the parent fragment peptide in vitro.

152 entify both nonbiotinylated and biotinylated peptides in a single experimental setup.

153 esin to facilitate the chemical synthesis of peptides in organic solvent as well as the enzymatic syn

154 re of acetylated/nonacetylated alpha-tubulin peptides in the background of human olfactory neurospher

155 shared and tumor-specific non-canonical HLA peptides, including an immunogenic peptide derived from

156 ollapsed interbilayer spacing resulting from peptide-induced adhesion.

157 is and across the cell layers in which these peptides influence patterns.

158 Many peptide inhibitors have been constructed from the variou

159 accurately predicting the affinities of PBD-peptide interactions across multiple protein families.

160 peline for future HTP measurements of domain-peptide interactions.

161 of target protein and employ isotope-labeled peptide internal standards to quantify chosen surrogate

162 The amyloid-beta peptide is correlated with Alzheimer's disease and is as

163 Capture and release of peptides is often a critical operation in the pathway to

164 cases, the binding between MHC and antigenic peptides is the most selective step in the antigen prese

165 rea under the concentration-time curve for C-peptide level in response to a 4-hour mixed-meal toleran

166 exchange MS), to characterize the global and peptide-level conformational changes.

167 ls (pSILAC), phosphoproteomics, and a unique peptide-level matching strategy, our DeltaSILAC profilin

168 NT-proBNP (N terminal pro B-type natriuretic peptide) levels were examined in multivariable-adjusted

169 (NRG1) is a large (> 60-amino-acid) natural peptide ligand for the ErbB protein family members HER3

170 MBRYO SURROUNDING REGION (ESR)-RELATED (CLE) peptide ligands in connection with their receptors are i

171 des a binding platform for 21 amino acid CIF peptide ligands, which are tyrosine sulfated by the tyro

172 itations of the tool and compare it to other peptide ligase enzymes.

173 Herein, we use a peptide ligase, butelase 1, to label the human transferr

174 Peptidomimetics can respond to peptide limitations by displaying higher metabolic stabi

175 e readily assembles with lipid vesicles into peptide/lipid coaggregates that resemble amyloid fibrils

176 SARS-CoV-2-specific CD8(+) T cells, applying peptide-loaded major histocompatibility complex class I

177 stratifies subjects for future severity of C-peptide loss after 1 year.

178 tion of TREM-1 in EV-A71-infected PBMCs with peptide LP17 resulted in decreased levels of pro-inflamm

179 ength numbering), were incorporated into the peptide macrocycles c[Pro(1)-Arg(2)-Phe(3)-Phe(4)-Xaa(5)

180 and panning for antigen-reactive TCRs using peptide major histocompatibility complex binding and cel

181 elective increase in TCR sensitivity to self-peptide MHC in vivo and an enhanced response to weak ago

182 a comprehensive in silico analysis of viral peptide-MHC class I binding affinity across 145 HLA-A, -

183 nalysis presented here can be applied to any peptide-MHC complex of interest with a structural model

184 of peptides and subsequently large bodies of peptide-MHC-II interaction data are key to the solution

185 Self-assembled peptide micelles and fibers demonstrate unique control o

186 ct of leptin, whereas a Src kinase activator peptide mimicked it.

187 nd affinity analyses, we designed two cyclic peptide mimics of the TAR-binding beta2-beta3 loop seque

188 Here, we show that constrained 31-residue-peptides ('msR4Ms') designed to mimic the CXCR4-binding

189 on of CeA slices with nociceptin/orphanin FQ peptide (N/OFQ; 500 nM), an endogenous opioid-like pepti

190 interactions of representative amyloidogenic peptides, namely, the 106-126 fragment of prion protein

191 Delivery of siRNA-peptide nanoplexes co-targeting MK2 and XPA to pre-exist

192 y organized supramolecular polymerization of peptide nanotubes was applied in the assembly of highly

193 broad class of macrocyclic, heavily modified peptide natural products that are unified by the presenc

194 Pore formation by membrane-active peptides, naturally encountered in innate immunity and i

195 e (N/OFQ; 500 nM), an endogenous opioid-like peptide, normalized GABA transmission in HA rats.

196 engineered with a novel and highly specific peptide nucleic acid (PNA) as the recognition element.

197 t can suit CE-based miRNA analysis utilizing peptide nucleic acid (PNA) hybridization probes.

198 the zein gene from maize using pyrrolidinyl peptide nucleic acid (PNA) immobilized on a magnetic sol

199 lysis, we identified six fractions with high peptide number and uniqueness that can account for 80% o

200 suggest that on reaching the cytoplasm, the peptide occupies its binding site prior to the transitio

201 We identify host-derived peptides of 4-11 residues, varying in both charge and co

202 The binding of amyloid-beta peptides of different concentrations to the surface of t

203 the form of a collection of conserved short peptides) of each subfamily, and thus were further used

204 T cells to kill tumor cells with target HLA/peptide on their surfaces in vitro.

205 akes use of a reactive linker to form cyclic peptides on the phage surface while simultaneously intro

206 ed the presence of only two short allergenic peptides on the surface of CpCP3, which was highly susce

207 olymer augments the efficacy of an oncolytic peptide (OP; KKWWKKWDipK) for immunotherapy by exploitin

208 ry input for the server consists of a set of peptides or proteins, optionally with PTM sites, and the

209 Application of this method to tryptic peptides originating from O-GlcNAcylated proteins TAB1 a

210 The NMR structure of the macrocyclic peptide overlays well with that of alpha-RgIA4, demonstr

211 In contrast to peptide P1, UV-irradiation of ubiquitin did not induce H

212 hibitor 3 (PI3), a gene in the antimicrobial peptide pathway and known to be involved in antimicrobia

213 y useful to increase the number of annotated peptide peaks with their corresponding amino acid sequen

214 iquitylation sites from as little as 500 mug peptide per sample from cells or tissue in a TMT10plex i

215 e observations demonstrate that our designed peptides perturb TJs in human lung as well as human and

216 Instead, the opioid peptides play complex and overlapping roles in a variety

217 and purification were tested and the tryptic peptide pools were analysed by untargeted high resolutio

218 or all coordinated depending on the ratio of peptide/porphyrin.

219 e a scan mode that samples up to 100% of the peptide precursor ion current in m/z and mobility window

220 ide activity, and genetic knockout of opioid peptide precursors.

221 Importantly, it should be noted that a peptide predicted with a higher binding score for a spec

222 Fifty T. cruzi peptides predicted to bind a broad range of class I and

223 oads, presumably due to increased breadth of peptide presentation.

224 ng factor (PDF), a neuromodulatory signaling peptide produced only by circadian clock circuit neurons

225 The peptide profile generated after in vitro and in vivo dig

226 and intestinal digestion for differences in peptide profiles and peptide bioactivities.

227 Unfortunately, matching peptide properties with their ability to selectively for

228 Both peptides protected greater than 80% mice from infection-

229 been used especially in chemical biology for peptide/protein synthesis, posttranslational modificatio

230 or various kinds of molecules including DNA, peptides, proteins, and oligosaccharides.

231 Here, we describe a methodology for targeted peptide quantification using a trapped ion mobility quad

232 inimum inhibitory concentration (MIC) of the peptide ranged from 80 mug/ml for X. citri to 600 mug/ml

233 at the soluble, nonfibrillizing Abeta (1-30) peptide recapitulates full-length Abeta stereoselective

234 Peptide receptor radionuclide therapy (PRRT) with (177)L

235 Conclusion: Peptide receptor radionuclide therapy can lead to bowel

236 Formyl-peptide receptors are highly expressed on neutrophils an

237 Peptides such as gastrin-releasing peptide receptors targeting radiopharmaceuticals are sma

238 Here, we show that opioid peptide receptors, GPCRs that mediate highly sensitive p

239 ydrides, for the synthesis of peptidyl-RNAs, peptides, RNA oligomers and primordial phospholipids.

240 ogical fit ensures that CDR3beta reaches the peptide's featured C-terminal segment for pMHC sampling,

241 believed to be activated by a lipid-sensing peptide(s) in the ER that can cluster PM-derived cholest

242 d IL10), and a proinflammatory antimicrobial peptide (S100A7).

243 , conferring entirely novel functions on the peptide scaffolds.

244 In this study, several families of peptides, selected for the ability to partition into and

245 promising the chromatographic performance of peptide separation.

246 we have investigated the effect of a shorter peptide sequence derived from Cpn 60.1, named IRL201104,

247 These rules can be generalized for other peptide sequences.

248 rs, using interferon-gamma-based assays with peptides spanning SARS-CoV-2 except ORF1.

249 Peptide stapling has benefited from the development of s

250 ating saccharides covalently cross-linked by peptide stems.

251 We interpret the increase in peptide storage in the fall and the shift to a more anti

252 This review covers the range of peptide studies done with VCD and extends them to compar

253 y inactive mutant in vivo (based on in vitro peptide studies) actually retains substantial H3K4 demet

254 achieve high selectivity when targeting the peptide substrate binding site of NTMT1/2.

255 Peptides such as gastrin-releasing peptide receptors tar

256 and also requires the presence of activator peptides, such as benzoyl-leucyl-leucine (Bz-LL), for fu

257 ing regardless of the presence of the leader peptide, suggesting that although the PEP domain serves

258 rganic solvents commonly used in polymer and peptide synthesis results in the alteration of DNA helic

259 eta-cells, we analyzed the HLA-A3-restricted peptides targeted by circulating CD8(+) T cells.

260 l disruption of the plasma membrane once the peptide targets specific phospholipids found on the cyto

261 Thrombin-derived C-terminal peptides (TCPs), including a major 11-kDa fragment (TCP9

262 oassembly process of PAP(248-286), a seminal peptide that displays both amyloid-forming and antimicro

263 rgeting approach is based on pHLIP, a unique peptide that selectively targets tumors in vivo by ancho

264 We investigate here a pH-sensitive peptide that self-assembles to form a hydrogel at neutra

265 function characterization, we present simple peptides that bind alpha-cobratoxin (alpha-Cbtx) and pre

266 Here we report the modification of two peptides that comprise a coiled-coil heterodimer pair wi

267 This PCSK9 inhibitor is one of many peptides that could benefit from bioactive cyclization,

268 on resonance, we identified parasite-derived peptides that have the sequence-specific ability to incr

269 e the development of novel anti-inflammatory peptides that therapeutically target the chemokine netwo

270 s and correctly identified >75% of HLA-bound peptides that were observed experimentally in 11 patient

271 h as specificity for aggregated forms of the peptide, the ability to distinguish polymorphic aggregat

272 udies were initially limited to simple model peptides, the past decade has seen a dramatic advancemen

273 he coating facilitated the mass transport of peptides through the PAN layer, thus enabling extraction

274 ontaining and UV-reduced cysteine-containing peptides to be identified by a nontargeted database sear

275 We used a set of natural peptides to explore the specificity of dissolved extrace

276 cs made by phospholipids and amphipathic 18A peptides to mediate the formation of supported phospholi

277 we study adhesion of Lys and DOPA-containing peptides to organic and inorganic substrates using singl

278 oemission spectroscopies, bonding of the two peptides to TiO(2) surfaces (either nanostructured or si

279 receptor inhibitor to the extent seen in ED peptide-treated female neurons.

280 We identify six antimicrobial peptides, two plant immune regulators and eight chemical

281 eveloped robust methods that integrate small-peptide units into designed scaffolds.

282 detection and identification of cross-linked peptides using multistage mass spectrometry (MS(n)).

283 ated as the separation media for analysis of peptides using supercritical fluid chromatography-mass s

284 d] and the presence of vasoactive intestinal peptide (VIP).

285 CD8 T cells against the immunodominant TMEV peptide VP2(121-130) Loss of H-2D(b) on CD11c(+) APCs mi

286 bovine serum albumin, glucose and elongated peptide) was negligible.

287 noted that these 1:1 alpha/Sulfono-gamma-AA peptides were completely resistant to proteolytic degrad

288 Two or more pathogen peptides were identified in 40% of samples from PTLDS an

289 Three of these peptides were purified and their structures elucidated b

290 The synthesized peptides were tested for their binding to nSH3/cSH3.

291 unds, representative of mono- and disulfated peptides, were used to compare the enrichment capabiliti

292 identified 53 differentially phosphorylated peptides when comparing low responders with high respond

293 n of the Toll pathway-mediated antimicrobial peptides when the flies were challenged with Gram-positi

294 ts, a class of Bronsted basic guanidinylated peptides, which catalyze an efficient atroposelective ch

295 thod in the case of the amyloid beta (Abeta) peptide, whose oligomers are associated with Alzheimer's

296 An RCL-derived peptide with the sequence Ser-Val-Ala-Phe-Ser (SVAFS) di

297 Peptides with the right properties, for example Antimicr

298 omeostatic control, and express insulin-like peptides with well-established roles in regulating food

299 The caveat is that modified peptides would need to reliably contain only a single O-

300 Administration of peptide YY to EEC-deficient mice restores normal electro