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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Language: | English |
Subjects: | Biochemistry, Digestive enzyme, Food digestion, Label-free quantification, Peptide release kinetics, Protease selectivity, Subsite model, Substrate inhibition, |
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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 |
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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 |
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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 |
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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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