AAV3 Titration ELISA 2.0R

Unique microtiter plate enzyme immunoassay for the quantitation of virions and assembled empty capsids of human Adeno-associated Virus 3. The recombinant capture-antibody detects a conformational epitope not present on unassembled capsid proteins. The assay represents a fast, sensitive and reproducible method for titration of intact AAV3B wt virions, AAV3B recombinant virions or assembled and intact empty AAV3B capsids.

The A20R antibody is used as capture and detection antibody in the AAV3 Titration ELISA 2.0R (PRAAV3R).

Please contact us at for specific academic pricing.

Background

The assay represents a fast, sensitive and reproducible method for titration of intact AAV3B wt virions, AAV3B recombinant virions or assembled and intact empty AAV3B capsids described in Rutledge at al., 1998.

Rutledge EA, Halbert CL and Russell DW. Infectious Clones and Vectors Derived from Adeno-Associated Virus (AAV) Serotypes Other Than AAV Type 2. Journal of Virology 72:309-319 (1998).

The ELISA principle:

The assay is based on the sandwich ELISA technique where a monoclonal antibody (mab) specific for a conformational epitope on assembled AAV capsids is coated onto the plate and is used to capture AAV particles from the specimen.

The detection of captured AAV particles is a two-step process.

A biotin-conjugated mab is bound to the captured AAV particles.
A streptavidin peroxidase conjugate reacts with the biotin molecules. The addition of the substrate results in a color reaction which is proportional to the amount of specifically bound viral particles.
Comparison of AAV Quantification Methods:

Each of the commonly used quantification methods has its pros and cons:

qPCR is widely used, but suffers from several issues such as sample preparation, primer design, or PCR efficiency that can lead to high inter-laboratory variation of results.
Digital droplet PCR methods overcome some of the limitations of qPCR. However, variations between labs can still occur due to different sample processing protocols.
Dot blot is a simple and quantitative method, if reliable reference material is used. However, it suffers from the limited linearity and dynamic range of western blotting in general.
Given the practical drawbacks of the aforementioned techniques, a conventional sandwich ELISA currently appears to be superior in terms of inter- and intralaboratory variation as well as ease of use. Therefore, it represents the best format for reliable and reproducible quantification of total rAVV capsid titers.

Use of shuffled/mutated AAV:

The recognition of shuffled/mutated AAV vectors depend on the specific capsid region which is affected by the shuffling/mutation. The capture antibodies used for PROGEN’s AAV ELISAs bind specific and, in some cases, well defined conformational epitopes. These epitopes are generated by the capsid assembly of the corresponding AAV serotypes. A first indication that the ELISA might recognize your shuffled/mutated AAV vector is the presence of the antibody-binding epitope. However, changes in the protein sequences of the capsid proteins might also influence conformation of the proteins, hence the conformation of the epitopes presented on the AAV capsid. This might influence binding affinity of the antibody and affect determination of the titer based on the (non-shuffled) Kit Control provided with the AAV ELISA kit. Since these properties strongly depend on the specific shuffling/mutation performed, PROGEN cannot guarantee successful and precise quantification of your shuffled/mutated AAV vector. Even if the antibody binding epitopes are still present on your shuffled/mutated AAV capsid, your assay needs to be tested and optimized for your specific AAV vector.

Highly recommends the production and calibration of a suitable (shuffled/mutated) Kit Control, to ensure reliable titer determination of your individually shuffled/mutated AAV vector with PROGEN ELISA kits.

More Details