Imino‐ and Azasugar Protonation Inside Human Acid β‐Glucosidase, the Enzyme that is Defective in Gaucher Disease

Publikation: Bidrag til tidsskriftLetterForskningfagfællebedømt

Standard

Imino‐ and Azasugar Protonation Inside Human Acid β‐Glucosidase, the Enzyme that is Defective in Gaucher Disease. / Matassini, Camilla; Warren, Julia; Wang, Bo; Goti, Andrea; Cardona, Francesca; Morrone, Amelia; Bols, Mikael.

I: Angewandte Chemie International Edition, Bind 59, Nr. 26, 2020, s. 10466-10469.

Publikation: Bidrag til tidsskriftLetterForskningfagfællebedømt

Harvard

Matassini, C, Warren, J, Wang, B, Goti, A, Cardona, F, Morrone, A & Bols, M 2020, 'Imino‐ and Azasugar Protonation Inside Human Acid β‐Glucosidase, the Enzyme that is Defective in Gaucher Disease', Angewandte Chemie International Edition, bind 59, nr. 26, s. 10466-10469. https://doi.org/10.1002/anie.202002850

APA

Matassini, C., Warren, J., Wang, B., Goti, A., Cardona, F., Morrone, A., & Bols, M. (2020). Imino‐ and Azasugar Protonation Inside Human Acid β‐Glucosidase, the Enzyme that is Defective in Gaucher Disease. Angewandte Chemie International Edition, 59(26), 10466-10469. https://doi.org/10.1002/anie.202002850

Vancouver

Matassini C, Warren J, Wang B, Goti A, Cardona F, Morrone A o.a. Imino‐ and Azasugar Protonation Inside Human Acid β‐Glucosidase, the Enzyme that is Defective in Gaucher Disease. Angewandte Chemie International Edition. 2020;59(26):10466-10469. https://doi.org/10.1002/anie.202002850

Author

Matassini, Camilla ; Warren, Julia ; Wang, Bo ; Goti, Andrea ; Cardona, Francesca ; Morrone, Amelia ; Bols, Mikael. / Imino‐ and Azasugar Protonation Inside Human Acid β‐Glucosidase, the Enzyme that is Defective in Gaucher Disease. I: Angewandte Chemie International Edition. 2020 ; Bind 59, Nr. 26. s. 10466-10469.

Bibtex

@article{abd177d78b4146379a37f107d96a4a42,
title = "Imino‐ and Azasugar Protonation Inside Human Acid β‐Glucosidase, the Enzyme that is Defective in Gaucher Disease",
abstract = "Gaucher disease is caused by mutations in human acid β‐glucosidase or glucocerebrosidase (GCase), the enzyme responsible for hydrolysis of glucosyl ceramide in the lysosomes. Imino‐ and azasugars such as 1‐deoxynojirimycin and isofagomine are strong inhibitors of the enzyme and are of interest in pharmacological chaperone therapy of the disease. Despite several crystal structures of the enzyme with the imino‐ and azasugars bound in the active site having been resolved, the actual acid–base chemistry of the binding is not known. In this study we show, using photoinduced electron transfer (PET), that 1‐deoxynojirimycin and isofagomine derivatives are protonated by human acid β‐glucosidase when bound, even if they are completely unprotonated outside the enzyme. While isofagomine derivative protonation to some degree was foreshadowed by earlier crystal structures, 1‐deoxynojirimycin derivatives were not believed to act as basic amines in the enzyme.",
author = "Camilla Matassini and Julia Warren and Bo Wang and Andrea Goti and Francesca Cardona and Amelia Morrone and Mikael Bols",
year = "2020",
doi = "10.1002/anie.202002850",
language = "English",
volume = "59",
pages = "10466--10469",
journal = "Angewandte Chemie International Edition",
issn = "1433-7851",
publisher = "Wiley-VCH Verlag GmbH & Co. KGaA",
number = "26",

}

RIS

TY - JOUR

T1 - Imino‐ and Azasugar Protonation Inside Human Acid β‐Glucosidase, the Enzyme that is Defective in Gaucher Disease

AU - Matassini, Camilla

AU - Warren, Julia

AU - Wang, Bo

AU - Goti, Andrea

AU - Cardona, Francesca

AU - Morrone, Amelia

AU - Bols, Mikael

PY - 2020

Y1 - 2020

N2 - Gaucher disease is caused by mutations in human acid β‐glucosidase or glucocerebrosidase (GCase), the enzyme responsible for hydrolysis of glucosyl ceramide in the lysosomes. Imino‐ and azasugars such as 1‐deoxynojirimycin and isofagomine are strong inhibitors of the enzyme and are of interest in pharmacological chaperone therapy of the disease. Despite several crystal structures of the enzyme with the imino‐ and azasugars bound in the active site having been resolved, the actual acid–base chemistry of the binding is not known. In this study we show, using photoinduced electron transfer (PET), that 1‐deoxynojirimycin and isofagomine derivatives are protonated by human acid β‐glucosidase when bound, even if they are completely unprotonated outside the enzyme. While isofagomine derivative protonation to some degree was foreshadowed by earlier crystal structures, 1‐deoxynojirimycin derivatives were not believed to act as basic amines in the enzyme.

AB - Gaucher disease is caused by mutations in human acid β‐glucosidase or glucocerebrosidase (GCase), the enzyme responsible for hydrolysis of glucosyl ceramide in the lysosomes. Imino‐ and azasugars such as 1‐deoxynojirimycin and isofagomine are strong inhibitors of the enzyme and are of interest in pharmacological chaperone therapy of the disease. Despite several crystal structures of the enzyme with the imino‐ and azasugars bound in the active site having been resolved, the actual acid–base chemistry of the binding is not known. In this study we show, using photoinduced electron transfer (PET), that 1‐deoxynojirimycin and isofagomine derivatives are protonated by human acid β‐glucosidase when bound, even if they are completely unprotonated outside the enzyme. While isofagomine derivative protonation to some degree was foreshadowed by earlier crystal structures, 1‐deoxynojirimycin derivatives were not believed to act as basic amines in the enzyme.

U2 - 10.1002/anie.202002850

DO - 10.1002/anie.202002850

M3 - Letter

C2 - 32191378

VL - 59

SP - 10466

EP - 10469

JO - Angewandte Chemie International Edition

JF - Angewandte Chemie International Edition

SN - 1433-7851

IS - 26

ER -

ID: 240411323