Virus Core Facility

Getting started

...how are AAVs produced
...workflow
...who is working on the production of the AAVs
Logo_Virus.jpg
© VCF

Information AAV

Eine Wissenschaftlerin und ein Wissenschaftler arbeiten hinter einer Glasfassade und mischen Chemikalien mit Großgeräten.
© Anne Quatraccioni

Adeno-associated viruses in research

A significant advantage of viruses is their capacity to penetrate cellular membranes and deliver DNA into the cell. This property is exploited in a research context to deliver transgenes into target cells both in vitro and in vivo. The Core Facility produces adeno-associated viruses for research purposes only.

Eine Wissenschaftlerin und ein Wissenschaftler arbeiten hinter einer Glasfassade und mischen Chemikalien mit Großgeräten.
© Rolf Müller

AAV expression plasmid

In recombinant AAVs, the viral genes are substituted by an expression cassette consisting of a promoter, the protein of interest, and regulatory elements. Two inverted terminal repeats flank this cassette that can comprise up to 4.7 kbp.

Virus Production
© Rolf Müller

Virus production and purification

In the Core Facility, we produce recombinant AAVs using the adenovirus-free helper production method. The AAV expression plasmid, the Rep/Cap encoding plasmid that defines the serotype of the AAV, and a plasmid encoding the necessary adenoviral helper genes are co-transfected to generate AAVs.

Gradient tube
© Larissa Kündgen

Virus serotypes

AAVs have several advantages, including the availability of different serotypes. These serotypes differ in their cellular tropism, allowing for targeted delivery to specific cell types and organs. The choice of purification method—either heparin affinity chromatography or iodixanol density gradient ultracentrifugation—depends on the particular serotype produced.

Workflow

Step 1

Contact Us

Reach out to us via email to discuss your project goals and specific requirements.

Step 2

Submit Request Form

Fill out our request form to initiate the project.

Step 3

Provide DNA

Drop off your DNA material, and we will start the plasmid cloning or virus production process.

Step 4

Pick up Virus

Once production is complete, you are welcome to pick up your DNA or virus.

Meet the Team

Get to know the Virus Core Facility Team that is responsible for managing and executing your project:

Avatar Kündgen

Larissa Kündgen

Core Facility Technician

Department for Epileptology, building 83

Venusberg-Campus 1

53127 Bonn

Avatar Quatraccioni

Dr. Anne Quatraccioni

Core Facility Manager

Department for Epileptology, building 83

Venusberg-Campus 1

53127 Bonn

Avatar Schoch  McGovern

Prof. Dr. Susanne Schoch  McGovern

Scientific Head

Department for Epileptology, building 83

Venusberg-Campus 1

53127 Bonn

Address

University Hospital Bonn
Virus Core Facility
Building 83, Basement
Venusberg-Campus 1
53127 Bonn
Please enter through the door
to the left of the yellow homunculus.

How to find us

190401_QRC_Epileptologie.jpg
© UKB

Arrival by bus and campus maps

From Bonn main station you can take the bus line 600 (direction Ippendorf Altenheim) and 601 (direction Venusberg) to the bus stop “Uniklinikum Süd”.

Further information including detailed maps can be found here.

Wird geladen