Insulin-Degrading Enzyme, an Under-Estimated Potential Target to Treat Cancer?
L Lesire, F Leroux, R Deprez-Poulain, B Deprez - Cells, 2022 - mdpi.com
Insulin-degrading enzyme (IDE) is a multifunctional protease due to the variety of its
substrates, its various cellular locations, its conservation between species and its many non …
substrates, its various cellular locations, its conservation between species and its many non …
The Insulin-Degrading Enzyme from Structure to Allosteric Modulation: New Perspectives for Drug Design
GR Tundo, G Grasso, M Persico, O Tkachuk, F Bellia… - Biomolecules, 2023 - mdpi.com
The insulin-degrading enzyme (IDE) is a Zn2+ peptidase originally discovered as the main
enzyme involved in the degradation of insulin and other amyloidogenic peptides, such as …
enzyme involved in the degradation of insulin and other amyloidogenic peptides, such as …
Insulin-degrading enzyme: Paradoxes and possibilities
MA Leissring - Cells, 2021 - mdpi.com
More than seven decades have passed since the discovery of a proteolytic activity within
crude tissue extracts that would become known as insulin-degrading enzyme (IDE) …
crude tissue extracts that would become known as insulin-degrading enzyme (IDE) …
An SPR-based method for Hill coefficient measurements: the case of insulin-degrading enzyme
A Distefano, G Antonio Zingale, G Grasso - Analytical and Bioanalytical …, 2022 - Springer
Insulin-degrading enzyme (IDE) is a highly conserved zinc metallopeptidase and is capable
to catalytically cleave several substrates besides insulin, playing a pivotal role in several …
to catalytically cleave several substrates besides insulin, playing a pivotal role in several …
Identification of indole-based activators of insulin degrading enzyme
N Kraupner, CP Dinh, X Wen, V Landry… - European Journal of …, 2022 - Elsevier
Insulin degrading enzyme (IDE) is a zinc metalloprotease that cleaves numerous substrates
among which amyloid-β and insulin. It has been linked through genetic studies to the risk of …
among which amyloid-β and insulin. It has been linked through genetic studies to the risk of …
Expanded Tools and Isosteres for Fragment-Based Drug Discovery against Metalloenzymes
H Seo - 2024 - search.proquest.com
Fragment-based drug discovery (FBDD) is a powerful approach for identifying molecules
that inhibit therapeutically relevant targets, focusing on the elaboration of fragment'hits' into …
that inhibit therapeutically relevant targets, focusing on the elaboration of fragment'hits' into …
Design of dual-action & selective Histone Deacetylase enzyme inhibitors
M Dennington - 2024 - etheses.dur.ac.uk
Carcinogenesis cannot be explained only by genetic alterations. Epigenetic processes such
as histone modification via (de) acetylation play a key role in gene expression, where …
as histone modification via (de) acetylation play a key role in gene expression, where …
Identification of Electrostatic Hotspots at the Binding Interface of Amylin and Insulin-Degrading Enzyme: A Structural and Biophysical Investigation
W Li - 2024 - preprints.org
Amylin, also known as islet amyloid polypeptide (IAPP), is a metabolic homeostasis-related
hormone that is produced and released by the β cells of the pancreas, the same cells that …
hormone that is produced and released by the β cells of the pancreas, the same cells that …