The path of proteolysis by bovine chymotrypsin

Chymotrypsin is one of the major proteases in intestinal protein digestion. Observations about the type of bonds that are hydrolysed (specificity and preference) were in the past derived from the peptide composition after digestion or hydrolysis rates of synthetic peptides. In this study, the path of hydrolysis by bovine chymotrypsin, i.e formation and degradation of peptides, were described for α-lactalbumin, β-lactoglobulin and β-casein. The peptide compositions, determined with UPLC-PDA-MS at different time points were used to determine the digestion kinetics for individual cleavage sites. It was evaluated how statements on (secondary) specificity from literature were reflected in the release kinetics of peptides. β-Lactoglobulin reached the highest degree of hydrolysis (10.9 ± 0.1 %) and was hydrolysed fastest (28 ± 1 mMpeptide bonds/s/mMenzyme), regardless of its globular (tertiary) structure. Chymotrypsin showed a preference towards aromatic amino acids, methionine and leucine, but was also tolerant to other amino acids. For the cleavage sites within this preference, ̴73% of the cleavage sites were hydrolysed with high or intermediate selectivity. For the missed cleavages within the preference, 45 % was explained by hindrance of proline, which affected hydrolysis only when in positions P3, P1′ or P2′. No clear indication (based on primary structure) was found to explain the other missed cleavages. A few cleavage sites were hydrolysed extremely efficient in α-lactalbumin (F9, F31, W104) and β-casein (W143, L163, F190). This study gave unique and quantitative insight in peptide formation and degradation by chymotrypsin in the digestion of proteins. The approach used showed potential to explore the path of hydrolysis for other proteases with less defined specificity.

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Main Authors: Vreeke, Gijs J.C., Vincken, Jean Paul, Wierenga, Peter A.
Format: Article/Letter to editor biblioteca
Language:English
Subjects:Biochemistry, Digestive enzyme, Food digestion, Label-free quantification, Peptide release kinetics, Protease selectivity, Subsite model, Substrate inhibition,
Online Access:https://research.wur.nl/en/publications/the-path-of-proteolysis-by-bovine-chymotrypsin
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spelling dig-wur-nl-wurpubs-6110682025-01-14 Vreeke, Gijs J.C. Vincken, Jean Paul Wierenga, Peter A. Article/Letter to editor Food Research International 165 (2023) ISSN: 0963-9969 The path of proteolysis by bovine chymotrypsin 2023 Chymotrypsin is one of the major proteases in intestinal protein digestion. Observations about the type of bonds that are hydrolysed (specificity and preference) were in the past derived from the peptide composition after digestion or hydrolysis rates of synthetic peptides. In this study, the path of hydrolysis by bovine chymotrypsin, i.e formation and degradation of peptides, were described for α-lactalbumin, β-lactoglobulin and β-casein. The peptide compositions, determined with UPLC-PDA-MS at different time points were used to determine the digestion kinetics for individual cleavage sites. It was evaluated how statements on (secondary) specificity from literature were reflected in the release kinetics of peptides. β-Lactoglobulin reached the highest degree of hydrolysis (10.9 ± 0.1 %) and was hydrolysed fastest (28 ± 1 mMpeptide bonds/s/mMenzyme), regardless of its globular (tertiary) structure. Chymotrypsin showed a preference towards aromatic amino acids, methionine and leucine, but was also tolerant to other amino acids. For the cleavage sites within this preference, ̴73% of the cleavage sites were hydrolysed with high or intermediate selectivity. For the missed cleavages within the preference, 45 % was explained by hindrance of proline, which affected hydrolysis only when in positions P3, P1′ or P2′. No clear indication (based on primary structure) was found to explain the other missed cleavages. A few cleavage sites were hydrolysed extremely efficient in α-lactalbumin (F9, F31, W104) and β-casein (W143, L163, F190). This study gave unique and quantitative insight in peptide formation and degradation by chymotrypsin in the digestion of proteins. The approach used showed potential to explore the path of hydrolysis for other proteases with less defined specificity. en application/pdf https://research.wur.nl/en/publications/the-path-of-proteolysis-by-bovine-chymotrypsin 10.1016/j.foodres.2023.112485 https://edepot.wur.nl/588012 Biochemistry Digestive enzyme Food digestion Label-free quantification Peptide release kinetics Protease selectivity Subsite model Substrate inhibition https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/ Wageningen University & Research
institution WUR NL
collection DSpace
country Países bajos
countrycode NL
component Bibliográfico
access En linea
databasecode dig-wur-nl
tag biblioteca
region Europa del Oeste
libraryname WUR Library Netherlands
language English
topic Biochemistry
Digestive enzyme
Food digestion
Label-free quantification
Peptide release kinetics
Protease selectivity
Subsite model
Substrate inhibition
Biochemistry
Digestive enzyme
Food digestion
Label-free quantification
Peptide release kinetics
Protease selectivity
Subsite model
Substrate inhibition
spellingShingle Biochemistry
Digestive enzyme
Food digestion
Label-free quantification
Peptide release kinetics
Protease selectivity
Subsite model
Substrate inhibition
Biochemistry
Digestive enzyme
Food digestion
Label-free quantification
Peptide release kinetics
Protease selectivity
Subsite model
Substrate inhibition
Vreeke, Gijs J.C.
Vincken, Jean Paul
Wierenga, Peter A.
The path of proteolysis by bovine chymotrypsin
description Chymotrypsin is one of the major proteases in intestinal protein digestion. Observations about the type of bonds that are hydrolysed (specificity and preference) were in the past derived from the peptide composition after digestion or hydrolysis rates of synthetic peptides. In this study, the path of hydrolysis by bovine chymotrypsin, i.e formation and degradation of peptides, were described for α-lactalbumin, β-lactoglobulin and β-casein. The peptide compositions, determined with UPLC-PDA-MS at different time points were used to determine the digestion kinetics for individual cleavage sites. It was evaluated how statements on (secondary) specificity from literature were reflected in the release kinetics of peptides. β-Lactoglobulin reached the highest degree of hydrolysis (10.9 ± 0.1 %) and was hydrolysed fastest (28 ± 1 mMpeptide bonds/s/mMenzyme), regardless of its globular (tertiary) structure. Chymotrypsin showed a preference towards aromatic amino acids, methionine and leucine, but was also tolerant to other amino acids. For the cleavage sites within this preference, ̴73% of the cleavage sites were hydrolysed with high or intermediate selectivity. For the missed cleavages within the preference, 45 % was explained by hindrance of proline, which affected hydrolysis only when in positions P3, P1′ or P2′. No clear indication (based on primary structure) was found to explain the other missed cleavages. A few cleavage sites were hydrolysed extremely efficient in α-lactalbumin (F9, F31, W104) and β-casein (W143, L163, F190). This study gave unique and quantitative insight in peptide formation and degradation by chymotrypsin in the digestion of proteins. The approach used showed potential to explore the path of hydrolysis for other proteases with less defined specificity.
format Article/Letter to editor
topic_facet Biochemistry
Digestive enzyme
Food digestion
Label-free quantification
Peptide release kinetics
Protease selectivity
Subsite model
Substrate inhibition
author Vreeke, Gijs J.C.
Vincken, Jean Paul
Wierenga, Peter A.
author_facet Vreeke, Gijs J.C.
Vincken, Jean Paul
Wierenga, Peter A.
author_sort Vreeke, Gijs J.C.
title The path of proteolysis by bovine chymotrypsin
title_short The path of proteolysis by bovine chymotrypsin
title_full The path of proteolysis by bovine chymotrypsin
title_fullStr The path of proteolysis by bovine chymotrypsin
title_full_unstemmed The path of proteolysis by bovine chymotrypsin
title_sort path of proteolysis by bovine chymotrypsin
url https://research.wur.nl/en/publications/the-path-of-proteolysis-by-bovine-chymotrypsin
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