ライフサイエンスコーパス: trypsin

1 ing molecular mass (melamine, vancomycin and trypsin).

2 equally well with or without the addition of trypsin.

3 by the accumulation of prematurely activated trypsin.

4 CK-8 and prevented accumulation of activated trypsin.

5 h large, rare motions of the loop regions in trypsin.

6 om crystals of the enzymes cyclophilin A and trypsin.

7 ified in camel milk proteins hydrolysed with trypsin.

8 iterraneus) was hydrolysed using Alcalase or trypsin.

9 that loop between the cold- and warm-active trypsin.

10 ydrolysis of pressure-treated proteins using trypsin.

11 psin B-dependent intracellular activation of trypsin.

12 The inhibitors specifically inhibited trypsin.

13 ults with enzymatic digestion of proteins by trypsin.

14 ng acetone followed by pellet digestion with trypsin.

15 les, through a mechanism dependent on active trypsin.

16 ion strategy over single step digestion with trypsin.

17 one inhibitor was determined in complex with trypsin.

18 and none suffered proteolytic degradation by trypsin.

19 l rates of analyte and standard digestion by trypsin.

20 ic digestion of the equine cytochrome c with trypsin.

21 This confirmed that the purified protein was trypsin.

22 thereby preventing accumulation of activated trypsin.

23 mpared it to the gold standard in the field, trypsin.

24 essed, BBI3, encodes a protein that inhibits trypsin.

25 behaves more similarly to subtilisin than to trypsin.

26 onspecific digestion of unfolded peptides by trypsin.

27 ter digesting the precipitated proteins with trypsin.

28 cleavage variants were observed relative to trypsin.

29 ons of just tens of seconds using the enzyme trypsin.

30 , in the same manner that aprotinin inhibits trypsin.

31 nce with the literature for the Nile tilapia trypsin.

32 Western corn rootworm (WCRW) midgut juice or trypsin, 100 fg/ml of the toxin was sufficient to form p

33 ular weight ( 7 kDa), followed by commercial trypsin (2.2 kDa) and visceral alkaline-proteases (1.75

34 he number of identified proteins compared to trypsin (8363 vs 6807; 1% protein FDR).

35 Trypsin, a high fidelity protease, is the most widely us

36 roteinase K, papain, alpha-chymotrypsin, and trypsin) abrogated entry, indicating that the SHFV cell

37 vels, are fully protected from intracellular trypsin accumulation and acinar damage.

38 n during pancreatitis triggers intracellular trypsin accumulation and loss of the early endosomal com

39 termination of the solution concentration of trypsin across the entire measurement range.

40 and shows that cytosolic cathepsin B but not trypsin activates cell death pathways.

41 Cytosolic cathepsin B but not trypsin activates the intrinsic pathway of apoptosis thr

42 However, the molecular events subsequent to trypsin activation and their role, if any, in cell death

43 e explored intra-acinar events downstream of trypsin activation that lead to acinar cell death.

44 vator of transcription 3 phosphorylation and trypsin activation were analyzed in isolated acinar cell

45 etion of cathepsin L increased intracellular trypsin activation.

46 us spectrophotometric rate determination for trypsin activity against the substrate N-benzoyl-DL-argi

47 system was synthesized along with improving trypsin activity and stability.

48 provides a simple method for fast-screening trypsin activity in aqueous solution.

49 The trypsin activity was measured as 9mU/mL by spectrophotom

50 In the last step, trypsin activity was measured by using Nalpha-Benzoyl-D,

51 own-regulation of digestive enzyme genes and trypsin activity, upon exposure to Tsp_PR-secreted facto

52 se activity, including specific increases in trypsin activity.

53 his study, serum albumin was hydrolysed with trypsin after several heat treatments and using differen

54 In HEK293 and KNRK cells, the PAR2 agonists trypsin and 2-furoyl-LIGRLO-NH2 activated PKD in the Gol

55 After 72 h at 40 degrees C, only trypsin and alpha-amylase maintained high activity.

56 entative mammalian digestive enzymes, namely trypsin and alpha-amylase.

57 Plasma samples were digested with trypsin and analyzed with liquid chromatography-tandem m

58 ters of milk samples have been digested with trypsin and chymotrypsin and analyzed by nanoLC-ESI-IT-M

59 as also stable and active in the presence of trypsin and chymotrypsin at pH 7.6, where pepsin C was c

60 ondary binding loop as compared with similar trypsin and chymotrypsin complexes.

61 slectin andSambucus nigralectin), proteases (trypsin and chymotrypsin), and glucosylceramide synthase

62 roteases in saliva differ biochemically from trypsin and chymotrypsin, and the cathepsins in the gut

63 the activity of two prototypical proteases, trypsin and chymotrypsin, as they diffuse down the lengt

64 otease assay also shows good specificity for trypsin and chymotrypsin.

65 ression of AOC3 is sensitive to digestion by trypsin and collagenase and that anti-AOC3 antibodies ca

66 (P<0.05) antioxidant activities compared to trypsin and HT, while trypsin and pepsin hydrolysates ex

67 ave generated antibodies that inhibit bovine trypsin and human neutrophil elastase (HNE) with low nan

68 low provides good sequence coverage for both trypsin and Lys C digests of bovine serum albumin, provi

69 in receptor-like kinase 5 is dispensable for trypsin and PAR2 activating peptide (PAR2-AP)-induced mi

70 activities compared to trypsin and HT, while trypsin and pepsin hydrolysates exhibited higher ACE-inh

71 ACE-inhibitory activity was generated in the trypsin and pepsin hydrolysates than in the HT hydrolysa

72 ers, the membrane proteins are digested with trypsin and quantitated by parallel reaction monitoring

73 of IGNIS prime peptides was optimised using trypsin and SMART Digest.

74 idin variants targeting the serine proteases trypsin and subtilisin.

75 od is an attractive alternative for assaying trypsin and the developed capacitive system might be use

76 Simultaneously, the protein is digested with trypsin and the resulting fragments are purified by HPLC

77 ine-proteases from Giant catfish, commercial trypsin, and Izyme AL(R).

78 -beta (TGF-beta), serine proteinases such as trypsin, and proteinase-activated receptor 2 (PAR2) prom

79 stion requires acid denaturation and pepsin, trypsin, and/or chymotrypsin cleavage.

80 ng surface rigidity in cold- and warm-active trypsins are demonstrated here by calculation of high-pr

81 ed monolayers (SAMs) on gold surfaces, using trypsin as a model protease.

82 Three enzymes, trypsin, AspN, and pepsin, were used separately to gener

83 After proteolysis with trypsin at pH 7 but not with pepsin at pH 2, a limited t

84 pensive, simple and fast procedure to purify trypsin based on affinity binding with ferromagnetic par

85 used to indirectly detect protease activity (trypsin) based on proteolytic digestion of protamine, an

86 lations of full ligand exit pathways for the trypsin-benzamidine system, generated using the sampling

87 miting steps in the paradigmatic case of the trypsin-benzamidine system.

88 Alpha-amylase/trypsin bi-functional inhibitors (ATIs) are non-gluten p

89 igand, is generally regarded as a target for trypsin but not for thrombin signaling.

90 ticles imprinted with an unrelated template (trypsin) but prepared with the same polymer composition.

91 free, real-time, easy and rapid detection of trypsin by using the microcontact imprinting method.

92 on previous work demonstrating that purified trypsin can activate NanI activity, this study next dete

93 liquid is required, as little as 1.2 fmol of trypsin can be detected by using the on-chip assay.

94 protein load by using Bradford assay and the trypsin-catalyzed hydrolysis of Nalpha-Benzoyl-dl-argini

95 phagic vacuoles and activation of proteases (trypsin, chymotrypsin).

96 increased the activity of CTSB, cathepsin L, trypsin, chymotrypsin, and caspase 3 in vivo and in vitr

97 ed by endogenous pancreatic protease such as trypsin, chymotrypsin, and elastase.

98 ious pepsin exposition promotes digestion by trypsin/chymotrypsin by exposing new cleavage sites.

99 cted their putative inhibitory activities to trypsin/chymotrypsin/elastase-like enzymes based on the

100 ealed in all cases the existence of a unique trypsin cleavage site within the membrane domain (out of

101 enhancement of Au photoelectron signal after trypsin cleavage were corresponding to the proposed mech

102 ferents demonstrated a selective response to trypsin cleavage.

103 tion conditions (buffer, digestion time, and trypsin concentration), chromatographic separation, and

104 igestion of the protein with enzymes such as trypsin could induce artifacts and modifications which w

105 Trypsin depleted PAR2-Kaede from the Golgi apparatus and

106 scopy, corresponding to a pre-equilibrium of trypsin deprotonation.

107 ication, providing a precision comparable to trypsin-despite broad specificity and fast digestion tha

108 Real-time trypsin detection was performed with trypsin-imprinted (

109 pacer were shown to be the best platform for trypsin detection, leading to the highest fidelity signa

110 liquid crystal (LC)-based sensor system for trypsin detection.

111 nted in the direct analysis of peptides from trypsin digested bovine serum albumin.

112 MS in a simple and efficient way; LC-MS of a trypsin-digested bovine serum albumin (BSA) sample provi

113 e ATRaS system works for complex mixtures of trypsin-digested cell lysate.

114 Trypsin-digested proteins from Saccharomyces cerevisiae

115 Trypsin-digested, SDA-cross-linked human serum albumin (

116 g a novel sample preparation procedure using trypsin digestion and a shotgun proteomics approach.

117 tree nuts have been extracted, subjected to trypsin digestion and analysis by liquid chromatography/

118 ion of sarcoplasmic proteins was followed by trypsin digestion and analysis by nanoliquid chromatogra

119 on as assessed by an enhanced sensitivity to trypsin digestion and by small angle x-ray scattering (S

120 Together with the trypsin digestion based LC-MS/MS analysis using surrogat

121 e also found that L2 protein is sensitive to trypsin digestion during infection.

122 quantification of a signature peptide after trypsin digestion of plasma samples before and after an

123 rders of magnitude less than the traditional trypsin digestion sample preparation procedure.

124 based on the use of accelerated in-solution trypsin digestion under an ultrasonic field provided by

125 arginine such that each peptide derived from trypsin digestion was labelled.

126 onic bath for digestion enhancement, on-bead trypsin digestion was optimized to obtain efficient and

127 y were (1) the hemolysis level, (2) stopping trypsin digestion with acid, and (3) the trypsin/protein

128 at 4 degrees C, stopping or not stopping the trypsin digestion with acid, the type of blood collectio

129 After isolation, trypsin digestion, and purification, peptides were fract

130 e triple helix to become highly sensitive to trypsin digestion.

131 nutes compared to 24 hours using in-solution trypsin digestion.

132 microvascular disease until 12 months, when trypsin digests and dye leakage assays showed high fat-f

133 y, we show that the introduced 170 loop from trypsin directly interacts with the FVIIa active site, s

134 ng (A83-01) and FGF2 (PD173074), followed by trypsin dissociation and recovery of colonies capable of

135 Trypsin (EC 3.4.21.4) was successfully immobilized on th

136 tachment, and because treatment of R36A with trypsin eliminated its inhibitory activity, we incubated

137 cessfully identified from pearl millet using trypsin enzyme.

138 ave direct relevance to other members of the trypsin fold.

139 ysis, the remaining samples were digested by trypsin, followed by SRM detection.

140 BP fractions were hydrolyzed with papain and trypsin for 3h at optimum conditions.

141 systems, which require addition of exogenous trypsin for continued propagation, VA1 could be propagat

142 omposite can be reused and applied to purify trypsin from other sources.

143 tructure and biochemical characterization of trypsin from the viscera of Liza aurata.

144 h HtrA2 showed minimal ApoE4 proteolysis and trypsin had no preference between ApoE4 and ApoE3.

145 d with those produced from commercial bovine trypsin (HB).

146 For pepsin and combined pepsin-trypsin hydrolyses, the highest degree of hydrolysis (DH

147 ed: encapsulated peptides are protected from trypsin hydrolysis, whereas physicochemically similar pe

148 ysis and sequential hydrolysis by pepsin and trypsin hydrolyzed all heavy molecular weight chains of

149 The trypsin-hydrolyzed denatured albumin exhibited the highe

150 The results suggest that trypsin-hydrolyzed denatured rice bran albumin might be

151 i.e., specific chemical sensing element) and trypsin (i.e., analyte), a model protease enzyme with re

152 nly 86% of identity with its most homologous trypsin II of the Salmo salar.

153 al-time trypsin detection was performed with trypsin-imprinted (trypsin-MIP) capacitive electrodes us

154 This report defines the role of trypsin in AP and shows that cytosolic cathepsin B but n

155 e on-chip protease assays are used to detect trypsin in buffer and serum.

156 for the target molecule (e.g., melamine and trypsin in our published work).

157 of other proteins and was sensitive towards trypsin in the clinically relevant range, with a Limit o

158 Notably, the prominent role of trypsins in the hydrolytic degradation of major allergen

159 e from other enzymes (e.g., chymotrypsin and trypsin) in the same family (E.C. 3.4.21).

160 been connected to trypsinogen activation or trypsin inactivation.

161 CER-based protein extract resulted in higher trypsin inhibiting activity, when compared to the indust

162 Trypsin inhibition did not affect apoptosis in hepatocyt

163 Raising the vesicular pH, but not trypsin inhibition, reduced CTSB activity.

164 ded to mutate two lysine residues to abolish trypsin inhibition, suggesting BBI3's mechanism of doubl

165 he antinutritional content of lectins (48%), trypsin inhibitor (57%), amylase inhibitor (49%) and phy

166 hibitors homologous to the bovine pancreatic trypsin inhibitor (BPTI) provide a suitable scaffold, bu

167 or plasma (PPP), either with or without corn trypsin inhibitor (CTI) to prevent contact activation, o

168 d found evidence for radiation of the Kunitz trypsin inhibitor (KTI) gene family within winged bean.

169 We also analyzed the soybean trypsin inhibitor (STI) gene family, important plant def

170 The determination of trypsin inhibitor (TI) activity is of importance to eval

171 sing a ladder of small-to-mid mass proteins (Trypsin Inhibitor (TI); Ovalbumin (OVA); Bovine Serum Al

172 esis of a functional analog of the Sunflower Trypsin Inhibitor 1.

173 ith isoflavone conversions and reductions in trypsin inhibitor activity.

174 We illustrate them using bovine pancreatic trypsin inhibitor and present a new, detailed analysis o

175 Phytic acid, tannins and trypsin inhibitor as antinutrients were detected.

176 annexin A1 protein grafted into a sunflower trypsin inhibitor cyclic scaffold.

177 her KLK5 activity by the inhibitor sunflower trypsin inhibitor G, restoration of DSG1 expression and

178 ar dynamics simulations on the cysteine-rich trypsin inhibitor MCoTI-II with three disulfide bridges.

179 in the cleavage of Kunitz-bovine pancreatic trypsin inhibitor protease inhibitors by mesotrypsin, fi

180 Human blood (corn trypsin inhibitor treated [4 mug/mL]) was tested by micr

181 rresponding to soybean agglutinin and Kunitz trypsin inhibitor were identified based on the statistic

182 ate, nitrite, cyanide, oxalate, phytate, and trypsin inhibitor) in tubers of Jerusalem artichokes-Kae

183 ticide residues (37 compounds), cyanide, and trypsin inhibitor, as well as Pb, Cd, nitrate, and nitri

184 thepsin G substrate sequences into sunflower trypsin inhibitor-1 (SFTI-1) produced a potent cathepsin

185 s) into the cyclic peptide SFTI-1 (sunflower trypsin inhibitor-1) and a heterodimeric 2S albumin.

186 s annuus PawS1 (preproalbumin with sunflower trypsin inhibitor-1) and provide new insights into the p

187 thetic inhibitor library (based on sunflower trypsin inhibitor-1) for characterizing the P2' specific

188 nhibitors based on Momordica cochinchinensis trypsin inhibitor-II.

189 rfusion (wall shear rate, 200 s(-1)) of corn trypsin inhibitor-treated whole blood over a 250-mum lon

190 ed with the heavy chains (HC) of inter-alpha-trypsin inhibitor.

191 -4 is 8.6 times higher than purified soybean trypsin inhibitor.

192 either cell-surface HA or serum inter-alpha-trypsin inhibitor.

193 Wheat amylase-trypsin inhibitors (ATIs) are nutritional activators of

194 BACKGROUND & AIMS: Wheat amylase-trypsin inhibitors (ATIs) are nutritional activators of

195 oncentrations of verbascoside, lignin and/or trypsin inhibitors, which decreased larval survival and/

196 d a significant reduction in the activity of trypsin inhibitors.

197 soflavone forms and the residual activity of trypsin inhibitors.

198 rsion of isoflavones and the inactivation of trypsin inhibitors.

199 The trypsin inhibitory activity of BG-4 is 8.6 times higher

200 The high trypsin inhibitory activity of BG-4 may be responsible f

201 eae) families, but peptides that mimic their trypsin-inhibitory loops exist in sunflowers (Helianthus

202 model for the enthalpy-driven all-d-peptide-trypsin interactions.

203 remarkable effect of turning the cold-active trypsin into a variant with mesophilic characteristics w

204 s mechanism, the limit of detection (LOD) of trypsin is 10 ng/mL, and it does not respond to thrombin

205 This report also suggests that trypsin is a requisite for AP only because it causes rel

206 ated trypsin-like serine proteases including trypsin itself could be further reduced.

207 potent activity against the serine protease trypsin (Ki = 1.5 nm).

208 A phylogenic analysis showed that L. aurata trypsin (LAT) is close to fish enzymes.

209 ues followed by cleavage of the peptide with trypsin led to a [2]rotaxane structure that self-assembl

210 The protease showed a trypsin-like activity with optimal temperature of 40 deg

211 Cockroach, like other allergens, contains trypsin-like enzyme activity that contributes to allerge

212 Human airway trypsin-like protease 4 (HAT-L4) is a type II transmembr

213 the visceral mass of M. charruana contains a trypsin-like protease that can generate peptides from ca

214 ated by cleavage of fibrinogen and PAR1, the trypsin-like protease thrombin activates the anticoagula

215 In this study, we investigated an additional trypsin-like protease, TMPRSS4.

216 o, we found an age-dependent decrease in the trypsin-like proteasomal activity in REGgamma-/- mice br

217 ed to identify, isolate and characterize the trypsin-like proteinases in German cockroach allergen ex

218 Testisin is a unique trypsin-like serine protease that is tethered to the ext

219 Factor D is a trypsin-like serine protease with a narrow specificity f

220 omplex of coagulation factor VIIa (FVIIa), a trypsin-like serine protease, and membrane-bound tissue

221 The trypsin-like serine protease, urokinase-type plasminogen

222 Although trypsin-like serine proteases have flexible surface-expo

223 ms and conformational flexibility of uPA and trypsin-like serine proteases in general.

224 lar range, and their potency against related trypsin-like serine proteases including trypsin itself c

225 R-2 is activated via proteolytic cleavage by trypsin-like serine proteases, including kallikrein-5 (K

226 aration steps were omitted by implementing a trypsin/Lys-C enzyme-immobilized multichannel reactor (M

227 hate buffer (0.1M, pH 7.5), whereas the free trypsin maintained about 64% of its initial activity dur

228 nteractions required for capsid assembly and trypsin-mediated proteolytic maturation needed for virus

229 nteractions required for capsid assembly and trypsin-mediated proteolytic maturation.

230 The trypsin-MIP capacitive electrode was used for ~80 assays

231 ection was performed with trypsin-imprinted (trypsin-MIP) capacitive electrodes using standard trypsi

232 sinopril and fosinoprilat) and two peptides (trypsin-modulating oostatic factor/TMOF and a bradykinin

233 Bead-displayed trypsin mutant genes were translated in droplets, the mu

234 in at 20 degrees C) prior to hydrolysis with trypsin only and trypsin-pronase.

235 sk any proteolytic cleavage sites of pepsin, trypsin or chymotrypsin.

236 ted, and processed into peptides with either trypsin or chymotrypsin.

237 olysis of the extracted proteins with either trypsin or HT generated more antioxidant activity than h

238 owing steps: PNGaseF treatment combined with trypsin or pepsin digestion was used to determine the gl

239 cial whey protein isolate (WPI) using either trypsin or Protamex(R) was compared using controlled (pH

240 In the absence of cholesterol, trypsin or proteinase K cleaved cytosolic loop 4, genera

241 ne-kinase (RTK) co-receptor) to chymotrypsin/trypsin or soluble ADAM.

242 of three enzymes - Alcalase, Flavourzyme, or trypsin - or by using a combination of two or three of t

243 late partially hydrolyzed with chymotrypsin, trypsin, or thermolysin retained about 80%, 30%, and 20%

244 tudy the pathogenesis of CP independently of trypsin pathways.

245 5 and 6, and were subjected to hydrolysis by trypsin, pepsin and a bacterial protease called HT for 1

246 by LC-MS analysis of fragments generated by trypsin plus endoprotease-Asp-N.

247 Finally, hydrolysates obtained using trypsin-pronase had a greater antioxidant capacity (ORAC

248 C) prior to hydrolysis with trypsin only and trypsin-pronase.

249 for the experimentalist to keep the ratio of trypsin/protein constant and to control the trypsin reac

250 ing trypsin digestion with acid, and (3) the trypsin/protein ratio.

251 number of freeze-thaw cycles, and different trypsin/protein ratios.

252 unds, the volatile (E)-alpha-bergamotene and trypsin proteinase inhibitors (TPIs), which are also fou

253 trypsin/protein constant and to control the trypsin reaction by stopping it with acid at an accurate

254 While trypsin remains the preferred enzyme for quantification

255 , and in this case perform quantification of trypsin-resistant proteins (C-hordeins) through analysis

256 y the inserted human sequence still formed a trypsin-resistant triple helix, suggesting a small local

257 unstable and slowly degradable peptides with trypsin, respectively, and suggested a one-site binding

258 Our results demonstrate that trypsin-sensitive (TS) breast and colon cancer cells sub

259 euraminidase- and chymotrypsin-resistant but trypsin-sensitive.

260 lts demonstrated a significant difference in trypsin sensitivity, which was linked to the E168K switc

261 in-MIP) capacitive electrodes using standard trypsin solutions in the concentration range of 1.0x10(-

262 Using a trypsin-specific activity-based probe, we detected three

263 e beneficial use of enzymes complementary to trypsin, such as Glu-C, Asp-N, Lys-N, Arg-C, LysargiNase

264 This trypsin susceptibility is consistent with the significan

265 in vitro gastrointestinal digestion (pepsin-trypsin system) greatly improved the antioxidant propert

266 oop swap variants containing the 170 loop of trypsin that display TF-independent enhanced activity.

267 n a comparison of inhibitors for the protein trypsin, the average KD values of benzamidine and benzyl

268 ne reduction, alkylation, and digestion with trypsin, the digests were eluted with 200 mM ammonium bi

269 ene-1-carboximidamide binding to the protein trypsin, the exchange term is found to be equal within e

270 h LC and immersed in the solution containing trypsin, the peptide bonds of BSA were hydrolyzed and pe

271 In this study trypsin (TIA) and chymotrypsin inhibitory (CIA) activiti

272 uding the PAR-2 ligands, mast cell tryptase, trypsin, tissue factor, and kallikrein (KLK) 5 and KLK14

273 t popular bottom-up proteomics workflow uses trypsin to enzymatically cleave proteins C-terminal to l

274 Immobilized trypsin (TR) was more stable than the free one and demon

275 iophysical properties of both the native and trypsin-treated forms of the toxin.

276 ns) was observed for the pores formed by the trypsin-treated toxin.

277 orms of the toxin (native, midgut juice- and trypsin-treated), with conductances ranging from 28 to 6

278 demonstrated by increased exposure following trypsin treatment.

279 loop of a CRN that produces oscillations of trypsin under out-of-equilibrium conditions.

280 a real food was investigated by immobilized trypsin using sodium dodecyl sulfate-polyacrylamide gel

281 nderstand the differential role of cytosolic trypsin vs cytosolic cathepsin B in activation of apopto

282 The cDNA of the mature trypsin was cloned and sequenced.

283 The performance of the immobilized trypsin was demonstrated by carrying out the hydrolysis

284 nd the cytosolic activity of cathepsin B and trypsin was evaluated.

285 Trypsin was leached off under high ionic strength (3M Na

286 Retinal digestion using trypsin was performed and acellular capillaries enumerat

287 In addition, activity of the immobilized trypsin was preserved 54.5% of its initial activity afte

288 Trypsin was strongly inhibited by serine protease inhibi

289 ing capacity, while prepared with commercial trypsin was the most effective in reducing ferric ions a

290 nd maximum reaction velocity (Vmax) for free trypsin were 5.1mM and 23mM/min, respectively, whereas K

291 y, whereas Km and Vmax values of immobilized trypsin were 7.88mM and 18.3mM/min, respectively.

292 pancreatic enzymes, such as chymotrypsin and trypsin, which are affected by the most common food pres

293 eolytic cleavage of redox-tagged peptides by trypsin, which causes the release of the redox reporter,

294 Trypsin, which increases open probability of the channel

295 s linker segment with the 99-hairpin loop of trypsin, which is absent in plasmin.

296 ed to a more rapid rate of WPI hydrolysis by trypsin, while the opposite was the case when Protamex(R

297 s show that DK and DTR motifs are cleaved by trypsin with 3 orders of magnitude lower speed than the

298 construction as well as the concentration of trypsin with which the hydrogel is loaded are investigat

299 structural features common with warm-active trypsins would explain why LAT acts at high temperatures

300 The digestion of ubiquitinated proteins with trypsin yields a glycine-glycine remnant bound to the mo