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Virus-like Particles (VLPs)

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Virus-like particles (VLPs) are highly structured protein particles formed by the self-assembly of single or multiple structural proteins of viruses, which are morphologically and structurally similar to natural viral particles and have strong immunogenicity and biological activity。Compared to conventional attenuated vaccines, VLPs lack regulatory proteins and infectious nucleic acids, have no replication capacity, are structurally similar to viral particles, and retain strong immunogenicity. This implies that VLPs vaccines are characterized by high safety and immunogenicity, and are a rather promising vaccine development strategy.

VLPs can be classified into the following two types:

Non-enveloped VLPs: Which are relatively simple structural VLPs consisting of single or multiple coat proteins that can be expressed in both prokaryotic and eukaryotic systems, such as human papillomavirus (HPV) VLPs vaccines.

Envelope VLPs:

Wrapped in a matrix of glycoprotein-containing lipid membranes derived from the host, which are more complex and challenging to produce, these complex VLPs are typically expressed in eukaryotic expression systems such as yeast, insect cells and plant cells, which require the co-expression of several structural proteins for the intracellular self-assembly process.


Types of VLPs (Yan D et al., Applied microbiology and biotechnology, 2015)


Non-enveloped VLPs monomeric proteins are usually expressed in E. coli or yeast, two systems that have the advantage of high expression and easy amplification. Enveloped VLPs require the lipid membrane structure of the expressed cell line during self-assembly and release, and are only suitable for eukaryotic expression, of which the baculovirus system is predominant.


Preparation process of VLPs (Lua LH et al., Biotechnology and bioengineering, 2014)

Service Content

Steps of service

Content

Delivery Period

Analysis and Solution Preparation

(1) Acquire customer requirements

(2) Analysis expression characteristics of VLPs

(3) Develop the program

1-2 Weeks

Vector construction

(1) Gene synthesis and codon optimization (optional)

(2) Fragment construction into suitable expression vectors

1-3 Weeks

Test expression and packaging

(1) Detection of protein expression

(2) Protein sample purification

(3) VLps assembly and purification

2-5 Weeks

Delivery material

(1) Protein samples

(2) Virus-like particle samples (If available)

(3) Project reports and product descriptions

1 Weeks

Service Process


Technical Advantage

(1) VLPs are very similar to natural viruses in terms of morphological structure and antigenicity, and thus can replace natural viral particles for immunoassays.

(2) VLPs have good structural plasticity and can be flexibly modified by chimerism or coupling to alter their tissue cell targeting or immunogenicity, allowing specific antigens to have the ability of VLPs to elicit a strong immune response from the organism.

(3) VLPs have the unique ability to carry DNA and other molecules and can serve as a vehicle for gene delivery.

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