Literature DB >> 29890260

Chemical modifications of insulin: Finding a compromise between stability and pharmaceutical performance.

Mohsen Akbarian1, Younes Ghasemi2, Vladimir N Uversky3, Reza Yousefi4.   

Abstract

Insulin, a key peptide hormone that conjointly with its receptor regulates blood glucose levels, is used as the major means to treat diabetes. This therapeutic hormone may undergo different chemical modifications during industrial processes, pharmaceutical formulation, and through its endogenous storage in the pancreatic β-cells. Insulin is highly sensitive to the environmental stresses and easily undergoes structural changes, being also able to unfold and aggregate. Even small changes altering the structural integrity of insulin may have important impact on the biological efficacy in relation to the physiological and pharmacological activities of this hormone. The chemical modifications of insulin may occur either randomly or based on the well-planned strategies to enhance its pharmaceutical properties. A plethora of studies have attempted to answer the fundamental questions of how chemical modifications and which environmental conditions may have either destructive effects or improve structural stability and pharmaceutical performance of insulin. The aim of this review is to highlight the impact of different modifications on structure, stability, biological activity, and pharmaceutical properties of insulin.
Copyright © 2018 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Aggregation; Biological efficacy; Chemical modification; Insulin structure; Stability

Mesh:

Substances:

Year:  2018        PMID: 29890260     DOI: 10.1016/j.ijpharm.2018.06.023

Source DB:  PubMed          Journal:  Int J Pharm        ISSN: 0378-5173            Impact factor:   5.875


  7 in total

1.  Modulating Insulin Fibrillation Using Engineered B-Chains with Mutated C-Termini.

Authors:  Mohsen Akbarian; Reza Yousefi; Ali Akbar Moosavi-Movahedi; Atta Ahmad; Vladimir N Uversky
Journal:  Biophys J       Date:  2019-09-23       Impact factor: 4.033

2.  Insulin amyloid polymorphs: implications for iatrogenic cytotoxicity.

Authors:  Keisuke Yuzu; Mikael Lindgren; Sofie Nyström; Jun Zhang; Wakako Mori; Risako Kunitomi; Terumasa Nagase; Keiichi Iwaya; Per Hammarström; Tamotsu Zako
Journal:  RSC Adv       Date:  2020-10-12       Impact factor: 4.036

3.  Inhibitory effect of coumarin and its analogs on insulin fibrillation /cytotoxicity is depend on oligomerization states of the protein.

Authors:  Mohsen Akbarian; Ehsan Rezaie; Fatemeh Farjadian; Zahra Bazyar; Mona Hosseini-Sarvari; Ehsan Malek Ara; Seyed Ali Mirhosseini; Jafar Amani
Journal:  RSC Adv       Date:  2020-10-16       Impact factor: 4.036

4.  Degradation of insulin amyloid by antibiotic minocycline and formation of toxic intermediates.

Authors:  Wakako Mori; Keisuke Yuzu; Nadine Lobsiger; Hideo Nishioka; Hisako Sato; Terumasa Nagase; Keiichi Iwaya; Mikael Lindgren; Tamotsu Zako
Journal:  Sci Rep       Date:  2021-03-25       Impact factor: 4.379

5.  Calculating the absolute binding free energy of the insulin dimer in an explicit solvent.

Authors:  Qiankun Gong; Haomiao Zhang; Haozhe Zhang; Changjun Chen
Journal:  RSC Adv       Date:  2020-01-03       Impact factor: 4.036

6.  Characterization of insulin cross-seeding: the underlying mechanism reveals seeding and denaturant-induced insulin fibrillation proceeds through structurally similar intermediates.

Authors:  Mohsen Akbarian; Maryam Kianpour; Reza Yousefi; Ali Akbar Moosavi-Movahedi
Journal:  RSC Adv       Date:  2020-08-13       Impact factor: 4.036

7.  The intriguing dose-dependent effect of selected amphiphilic compounds on insulin amyloid aggregation: Focus on a cholesterol-based detergent, Chobimalt.

Authors:  Katarina Siposova; Viktor I Petrenko; Ivana Garcarova; Dagmar Sedlakova; László Almásy; Olena A Kyzyma; Manfred Kriechbaum; Andrey Musatov
Journal:  Front Mol Biosci       Date:  2022-08-19
  7 in total

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