Literature DB >> 32627609

Improving protein glycan coupling technology (PGCT) for glycoconjugate vaccine production.

Jennifer Mhairi Dow1, Marta Mauri1, Timothy Alexander Scott1, Brendan William Wren1.   

Abstract

INTRODUCTION: Vaccines are one of the great success stories of modern medicine and an increasingly important strategy in the fight against antimicrobial resistance. Glycoconjugate vaccines, consisting of a protein component covalently linked to a glycan antigen, are extremely efficacious in preventing infectious disease. However, glycoconjugates have yet to reach their full potential, with currently licensed glycoconjugate vaccines available against only four pathogens. Protein glycan coupling technology, where glycoconjugates are biologically produced in purpose engineered bacterial cells, has the potential to revolutionize the field by lowering manufacturing cost and increasing flexibility for tailor-made vaccines. AREAS COVERED: This review gives an overview of the past 20 years of PGCT research, discusses the key developments and current status of the technology, and speculates on the future of PGCT-based vaccinology. EXPERT OPINION: PCGT has the potential to overcome some of the limitations of chemical conjugation production methods. The technology has undergone significant development since its inception, and new discoveries are continually driving the field forward. Vaccines currently in clinical trials have demonstrated the potential of the PGCT to deliver effective glycoconjugate vaccines for unmet medical needs.

Entities:  

Keywords:  Bacterial vaccines; PGCT; bioconjugation; glycoconjugate vaccines; glycoengineering

Mesh:

Substances:

Year:  2020        PMID: 32627609     DOI: 10.1080/14760584.2020.1775077

Source DB:  PubMed          Journal:  Expert Rev Vaccines        ISSN: 1476-0584            Impact factor:   5.217


  6 in total

1.  Engineering a suite of E. coli strains for enhanced expression of bacterial polysaccharides and glycoconjugate vaccines.

Authors:  Emily J Kay; Marta Mauri; Sam J Willcocks; Timothy A Scott; Jon Cuccui; Brendan W Wren
Journal:  Microb Cell Fact       Date:  2022-04-21       Impact factor: 6.352

2.  PglB function and glycosylation efficiency is temperature dependent when the pgl locus is integrated in the Escherichia coli chromosome.

Authors:  Vanessa S Terra; Marta Mauri; Thippeswamy H Sannasiddappa; Alexander A Smith; Mark P Stevens; Andrew J Grant; Brendan W Wren; Jon Cuccui
Journal:  Microb Cell Fact       Date:  2022-01-05       Impact factor: 5.328

3.  Glycan and Protein Analysis of Glycoengineered Bacterial E. coli Vaccines by MALDI-in-Source Decay FT-ICR Mass Spectrometry.

Authors:  Simone Nicolardi; Renzo Danuser; Viktoria Dotz; Elena Domínguez-Vega; Ali Al Kaabi; Michel Beurret; Chakkumkal Anish; Manfred Wuhrer
Journal:  Anal Chem       Date:  2022-03-16       Impact factor: 6.986

4.  Development of an automated platform for the optimal production of glycoconjugate vaccines expressed in Escherichia coli.

Authors:  Jasmin J Samaras; Marta Mauri; Emily J Kay; Brendan W Wren; Martina Micheletti
Journal:  Microb Cell Fact       Date:  2021-05-24       Impact factor: 6.352

5.  A minimal sequon sufficient for O-linked glycosylation by the versatile oligosaccharyltransferase PglS.

Authors:  Cory J Knoot; Lloyd S Robinson; Christian M Harding
Journal:  Glycobiology       Date:  2021-09-20       Impact factor: 4.313

6.  Multivalent poultry vaccine development using Protein Glycan Coupling Technology.

Authors:  Marta Mauri; Thippeswamy H Sannasiddappa; Prerna Vohra; Mark P Stevens; Andrew J Grant; Jon Cuccui; Brendan W Wren; Ricardo Corona-Torres; Alexander A Smith; Cosmin Chintoan-Uta; Abi Bremner; Vanessa S Terra; Sherif Abouelhadid
Journal:  Microb Cell Fact       Date:  2021-10-02       Impact factor: 5.328

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.