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Related Concept Videos

COP Coated Vesicles00:59

COP Coated Vesicles

Membrane-enclosed structures called vesicles transport proteins and lipids across the cell. The vesicles derive their cargo from the plasma membrane, Golgi, ER, or endosome. Coated vesicles are spherical, protein-coated carriers with a 50–100 nm diameter that mediate bidirectional transport between the ER and the Golgi. The distribution of proteins between the ER and Golgi complex is dynamic and is maintained by different coated vesicles. Their formation is driven by the assembly of different...
Clathrin Coated Vesicles01:12

Clathrin Coated Vesicles

Clathrin-coated vesicles use endocytosis to transport receptors and lysosomal hydrolases from the Golgi to the lysosome in the late secretory pathway. Clathrin-mediated endocytosis was the first described endocytic process, and Clathrin-coated vesicles remain one of the most well-studied transport vesicles. The molecular machinery that generates clathrin-coated vesicles comprises over 50 proteins that precisely coordinate vesicle formation. Cell surface receptors concentrated in indented sites...
Receptor-mediated Endocytosis01:20

Receptor-mediated Endocytosis

Receptor-mediated endocytosis is when bulk amounts of specific molecules are imported into a cell after binding to cell surface receptors. The molecules bound to these receptors are taken into the cell through inward folding of the cell surface membrane, which is eventually pinched off into a vesicle within the cell. Structural proteins, such as clathrin, coat the budding vesicle.
Clathrin-Mediated Endocytosis of LDL
One well-characterized example of receptor-mediated endocytosis is the...
Receptor-mediated Endocytosis01:38

Receptor-mediated Endocytosis

Overview
Eukaryotic Compartmentalization01:37

Eukaryotic Compartmentalization

One of the distinguishing features of eukaryotic cells is that they contain membrane-bound organelles, such as the nucleus and mitochondria, that carry out specialized functions. Since biological membranes are only selectively permeable to solutes, they help create a compartment with controlled conditions inside an organelle. These microenvironments are tailored to the organelle's specific functions and help isolate them from the surrounding cytosol.
For example, lysosomes in the animal cells...
Eukaryotic Compartmentalizations01:46

Eukaryotic Compartmentalizations

One of the distinguishing features of eukaryotic cells is that they contain membrane-bound organelles, such as the nucleus and mitochondria, that carry out specialized functions. Since biological membranes are only selectively permeable to solutes, they help create a compartment with controlled conditions inside an organelle. These microenvironments are tailored to the organelle's specific functions and help isolate them from the surrounding cytosol.
For example, lysosomes in the animal cells...

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Related Experiment Video

Updated: Jun 6, 2026

Assembly and Characterization of Polyelectrolyte Complex Micelles
08:44

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Published on: March 2, 2020

Sonochemically born proteinaceous micro- and nanocapsules.

Elena D Vassileva1, Neli S Koseva

  • 1St. Kliment Ohridsky University of Sofia, Bulgaria.

Advances in Protein Chemistry and Structural Biology
|November 27, 2010
PubMed
Summary

Ultrasound technology enables the simple, one-step fabrication of biocompatible protein micro- and nanocapsules. These versatile particles offer potential in diverse biomedical applications due to their unique properties.

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Last Updated: Jun 6, 2026

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Area of Science:

  • Biomaterials Science
  • Sonochemistry
  • Nanotechnology

Background:

  • Protein-based micro- and nanoparticles are increasingly utilized in biomedical fields due to their biocompatibility and biodegradability.
  • Applications range from drug delivery and imaging contrast agents to dietary products.
  • Ultrasound irradiation is a scalable, cost-effective, and environmentally friendly technique with diverse applications.

Purpose of the Study:

  • To review the current state-of-the-art in sonochemically produced protein micro- and nanocapsules.
  • To elucidate the mechanisms of formation, influencing factors, and applications of these particles.
  • To identify current challenges in the field of ultrasound-protein interactions for capsule fabrication.

Main Methods:

  • Fabrication of protein micro- and nanocapsules via ultrasound irradiation of aqueous protein solutions.
  • Analysis of acoustically generated cavitation and its role in chemical changes (e.g., sulfhydryl oxidation).
  • Investigation of protein denaturation and hydrophobic interactions driving capsule formation.

Main Results:

  • Ultrasound provides a facile one-step method for producing proteinaceous micro- and nanocapsules.
  • Acoustic cavitation induces chemical modifications and partial protein denaturation, leading to stable capsule formation.
  • Factors influencing capsule characteristics and their current applications in various biomedical fields are discussed.

Conclusions:

  • Sonochemistry offers a promising route for engineering protein-based micro- and nanocapsules.
  • Understanding ultrasound-protein interactions is crucial for optimizing particle characteristics and applications.
  • Further research is needed to address challenges and fully exploit the potential of these advanced biomaterials.