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Insulin Secretory Vesicles01:05

Insulin Secretory Vesicles

Insulin secretory vesicles release insulin to stimulate blood glucose uptake and regulate carbohydrate metabolism. When the blood glucose levels increase, glucose enters the pancreatic β-islet cells through glucose transporters. Once inside, glucose is metabolized through glycolysis, the citric acid cycle, and the electron transport chain, producing ATP. This increase in ATP concentration closes ATP-sensitive potassium channels, leading to depolarization of the membrane and the opening of...
Glucose Homeostasis: Pancreatic Islets and Insulin Secretion01:27

Glucose Homeostasis: Pancreatic Islets and Insulin Secretion

The pancreatic islets comprising only 1%-2% of the volume are highly vascularized and innervated mini-organs. They contain five endocrine cell types, including β cells that secrete insulin, which is synthesized as a single polypeptide chain, preproinsulin, processed to proinsulin, and finally to insulin and C-peptide. This process is complex and regulated, involving the Golgi complex, the endoplasmic reticulum, and the secretory granules of the β cell.
Insulin and C-peptide are co-secreted in...
Insulin: The Receptor and Signaling Pathways01:28

Insulin: The Receptor and Signaling Pathways

Insulin action is mediated through a receptor tyrosine kinase, akin to the IGF-1 receptor. The number of receptors per cell varies significantly, from 40 on erythrocytes to 300,000 on adipocytes and hepatocytes. The insulin receptor consists of linked α/β subunit dimers, forming a heterotetramer glycoprotein with two extracellular α subunits and two β subunits spanning the membrane. The α subunits inhibit the inherent tyrosine kinase activity of the β subunits, but this inhibition is released...
Insulin: Biosynthesis, Chemistry, and Preparation01:25

Insulin: Biosynthesis, Chemistry, and Preparation

The endoplasmic reticulum (ER) of pancreatic β-cells synthesizes preproinsulin, which consists of a signal peptide, A and B chains, and a C-peptide. Preproinsulin is then cleaved and folded into proinsulin, which translocates to the Golgi apparatus for sorting and packaging into secretory granules. In these granules, enzymatic clipping generates insulin and C-peptide.
Damage or functional impairment of β-cells inhibits insulin production, leading to diabetes. Diabetes treatment primarily uses...
Insulin Formulations: Types and Delivery01:27

Insulin Formulations: Types and Delivery

Insulin preparations are categorized by their duration of action into short-acting and long-acting types. Two strategies are used to modify insulin's absorption and pharmacokinetic profile: slowing the absorption post-subcutaneous injection, or altering human insulin's amino acid sequence or protein structure. These changes retain the insulin's ability to bind to the insulin receptor, but alter its behavior in solution or after injection.
Short-acting insulins are divided into rapid-acting...
Production of Pharmaceuticals01:30

Production of Pharmaceuticals

Industrial insulin production uses genetically engineered E. coli expressing a proinsulin gene controlled by a tryptophan promoter and containing a methionine linker for later cleavage. The cells also carry ampicillin resistance for selective growth. Seed cultures are stored at −80 °C and production begins by thawing a small amount to inoculate starter cultures, which are progressively scaled to a 50,000-L bioreactor. In the bioreactor, E. coli grow in nutrient-rich media under sterile, tightly...

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Related Experiment Video

Updated: May 9, 2026

An In Ovo Model for Testing Insulin-mimetic Compounds
06:09

An In Ovo Model for Testing Insulin-mimetic Compounds

Published on: April 23, 2018

Reversible insulin self-assembly under carbohydrate control.

Thomas Hoeg-Jensen1, Svend Havelund, Peter K Nielsen

  • 1Novo Nordisk, Novo Alle 6B2.54, DK-2880 Bagsvaerd, Denmark. tshj@novonordisk.com

Journal of the American Chemical Society
|April 28, 2005
PubMed
Summary

Insulin self-assembly can be controlled by carbohydrates. This carbohydrate-controlled protein self-assembly has potential for drug delivery applications.

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Last Updated: May 9, 2026

An In Ovo Model for Testing Insulin-mimetic Compounds
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Homogeneous Time-resolved Förster Resonance Energy Transfer-based Assay for Detection of Insulin Secretion
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Homogeneous Time-resolved Förster Resonance Energy Transfer-based Assay for Detection of Insulin Secretion

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Human Pseudoislet System for Synchronous Assessment of Fluorescent Biosensor Dynamics and Hormone Secretory Profiles
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Human Pseudoislet System for Synchronous Assessment of Fluorescent Biosensor Dynamics and Hormone Secretory Profiles

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Area of Science:

  • Biochemistry
  • Materials Science
  • Drug Delivery

Background:

  • Protein and peptide therapeutics offer significant clinical benefits.
  • Controlling the solubility and release kinetics of protein-based drugs is a major challenge.
  • Existing methods for protein stabilization and controlled release are often complex or limited in scope.

Purpose of the Study:

  • To develop a novel method for creating soluble, high molecular weight self-assemblies of insulin.
  • To demonstrate carbohydrate-mediated control over these insulin self-assemblies.
  • To explore the potential of this system for protein/peptide stabilization and controlled drug release.

Main Methods:

  • Synthesizing insulin derivatives with integrated boronate and polyol functionalities.
  • Investigating the self-assembly behavior of modified insulin in response to varying carbohydrate concentrations.
  • Characterizing the size, solubility, and stability of the resulting self-assemblies using biophysical techniques.

Main Results:

  • Insulin modified with boronates and polyols formed soluble, high molecular weight self-assemblies.
  • The self-assembly process was reversibly controlled by the presence and concentration of specific carbohydrates.
  • The system demonstrated potential for sustained release of insulin.

Conclusions:

  • Carbohydrate-responsive self-assembly offers a promising strategy for protein and peptide stabilization.
  • This approach provides a tunable platform for controlled drug release applications.
  • The principle illustrated has broad implications for the development of advanced protein-based therapeutics.