Title: Virus-like particles
1Virus-Like Particles Based Vaccines
2Content
03.
Culture Modes
3Part 01
Types of Virus-like Particles
4Types of Virus-like Particles
Virus-like particles consist of one or more
structural proteins that, when expressed
recombinantly, have the ability to self-assemble.
Proteins can be arranged in single, double or
triple layers. The VLPs of human papilloma virus
(HPV) are formed by a single structural protein
that forms the basic capsid of the particle.
Other more complex VLPs contain several
structural proteins. For example, the VLPs of the
Reoviridae family are formed by two to four
different proteins arranged in several layers.
VLPs may have an external lipid envelope such as
HIV-1 VLPs. Influenza virus VLPs are also formed
by the protein core and hemagglutinin spikes
which are displayed on its surface. 1 Since
envelope-VLPs will contain proteins expressed on
their membranes, the choice of producer cell line
will be crucial.
5Types of Virus-like Particles
Different virus-like particles
6Part 02
Production Methods
7Production Methods
8Part 03
Culture Modes
9Culture Modes
- Batch mode the most used culture mode and has
been used for many types of VLP, including HIV,
Chikungunya virus, and Ebola virus. All the
elements needed are added at the beginning of the
culture with the advantage that the medium is
well utilized, and the product is highly
concentrated. - Fed-batch mode small quantities of nutrients or
medium are added during the culture to supply the
cells with specific components depleted. Such
strategies can extend the exponential growth
phase and be used to reach high cell
concentrations. - Continuous cultivation mode fresh medium is
added while the conditioned medium is extracted.
This system presents a short turn-around time
(reduces the cost associated with cleaning and
filling of the bioreactor) and a small number of
production steps. However, continuous production
requires large amounts of medium, which is hard
to adapted to large-scale production. - Perfusion mode large volumes of media and
cell-medium separation devices are needed.
Although enhancing cellular growth and protein
expression, the perfusion system impact
negatively on cellular growth rate, protein
expression and production cost.
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