Related Experiment Video
Updated: Feb 7, 2026

Development and Assessment of Intracellular Infection Models for Staphylococcus aureus
Published on: January 17, 2025
In situ regeneration of bioactive coatings enabled by an evolved Staphylococcus aureus sortase A
Hyun Ok Ham1, Zheng Qu1,2, Carolyn A Haller1
1Department of Surgery, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215, USA.
This study introduces a novel method to regenerate bioactive films on medical devices using a reversible enzyme. This technique allows for repeated restoration of film function, extending device lifespan and improving clinical performance.
Area of Science:
- Biomaterials Science
- Surface Chemistry
- Enzyme Engineering
Background:
- Surface immobilization of bioactive molecules is crucial for implantable devices and biosensors.
- In vivo degradation limits the long-term performance of current bioactive films.
Purpose of the Study:
- To develop a method for repeatedly regenerating immobilized bioactive films.
- To enhance the longevity and in vivo performance of medical device coatings.
Main Methods:
- Utilized a laboratory-evolved Staphylococcus aureus sortase A (eSrtA) for reversible transpeptidation.
- Developed a two-step stripping and recharging cycle for film regeneration.
- Tested regeneration in the presence of whole blood and in situ after implantation.
Main Results:
- Demonstrated repeated regeneration of covalently immobilized monomolecular films.
- Preserved biological activity of anti-thrombogenic films through multiple regeneration cycles.
- Showcased in situ surface re-engineering of medical devices post-implantation.
Conclusions:
- Established a rapid, orthogonal, and reversible biochemical scheme for regenerating bioactive films.
- The eSrtA-mediated approach has the potential to significantly extend the lifetime of bioactive films on medical devices.
- This method enables surface modification and restoration of medical devices in vivo.
Related Concept Videos
Pinching-off of Coated Vesicles
Clathrin Coated Vesicles
COP Coated Vesicles
Coat Assembly and GTPases
Coat assembly depends on the local availability of phosphatidylinositol phosphates or PIPs and GTP-binding proteins. Adaptor proteins, which link the coat proteins to the membrane, bind to these PIPs and play a crucial role in controlling...
Whole Body Regeneration
Liver Regeneration
Cells of Liver
The liver comprises four major types of cells— hepatocytes, stellate, Kupffer, and sinusoidal endothelial cells. The hepatocytes are...

