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Extraction of Lysozyme from Chicken Albumen Using Polyelectrolyte Complexes
Jéré J van Lente1, Saskia Lindhoud2
1Department of Molecules & Materials, Membrane Science & Technology cluster, Nanobiophysics Group and MESA+ Institute for Nanotechnology, University of Twente, Drienerlolaan 5, Enschede, 7522 NB, The Netherlands.
Small (Weinheim an Der Bergstrasse, Germany)
|December 8, 2021
Summary
Polyelectrolyte complexes (PECs) mimic cell membrane-less organelles for selective protein extraction. Certain PECs efficiently uptake and release lysozyme, retaining its activity, demonstrating their potential as protein extraction media.
Area of Science:
- Biomimicry
- Materials Science
- Biochemistry
Background:
- Cells utilize membrane-less organelles (MLOs) for molecular compartmentalization and uptake.
- MLOs can be mimicked by polyelectrolyte complexes (PECs) composed of oppositely charged polymers.
- Protein uptake by PECs is highly dependent on their composition.
Purpose of the Study:
- To investigate the partitioning of lysozyme within four different PEC systems.
- To explore the selective extraction of proteins from mixtures using PECs.
- To evaluate the release properties and retained activity of extracted proteins.
Main Methods:
- Studied lysozyme partitioning in PECs with varying weak and strong polyelectrolyte combinations.
- Investigated lysozyme release by altering salt concentration (up to 500 mM NaCl) and pH (from 7 to 4).
- Utilized optimized PECs for selective lysozyme extraction from a hen-egg white protein matrix.
Main Results:
- All PEC systems exhibited similar trends in lysozyme partitioning based on complex composition.
- PECs formed from poly(allylamine hydrochloride) and poly(acrylic acid) showed optimal uptake and release.
- Selective extraction of lysozyme was achieved from a complex protein mixture.
Conclusions:
- Polyelectrolyte complexes can effectively mimic membrane-less organelles for selective protein uptake and release.
- The composition of PECs critically influences their protein extraction capabilities.
- Extracted lysozyme maintained its enzymatic activity, validating PECs as functional protein extraction media.

