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Dual-function antimicrobial-antibiofilm peptide hybrid to tackle biofilm-forming Staphylococcus epidermidis
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Metadata
Document Title
Dual-function antimicrobial-antibiofilm peptide hybrid to tackle biofilm-forming Staphylococcus epidermidis
Author
Wongchai M., Wongkaewkhiaw S., Kanthawong S., Roytrakul S., Aunpad R.
Affiliations
Facultad de Ciencias Qu?micas, Universidad Aut?noma de San Luis Potos?, Av. Dr. Manuel Nava 6, San Luis Potos?, 78210, Mexico; Secci?n de Biotecnolog?a, Centro de Investigaci?n en Ciencias de la Salud y Biomedicina, Universidad Aut?noma de San Luis Potos?, Av. Sierra Leona 550, Lomas 2a Secci?n, San Luis Potos?, 78210, Mexico; Virology and Cell Technology Laboratory, National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, 113 Thailand Science Park Phaholyothin Rd, Klong 1, Pathumthani, Klong Luang, 12120, Thailand; Secci?n de Microscop?a de Alta Resoluci?n, Centro de Investigaci?n en Ciencias de la Salud y Biomedicina, Universidad Aut?noma de San Luis Potos?, Av. Sierra Leona 550, Lomas 2a Secci?n, San Luis Potos?, 78210, Mexico; Secci?n de Medicina Molecular y Translacional, Centro de Investigaci?n en Ciencias de la Salud y Biomedicina, Universidad Aut?noma de San Luis Potos?, Av. Sierra Leona 550, Lomas 2a. Secci?n, San Luis Potos?, 78210, Mexico; Facultad de Ciencias, Universidad Aut?noma de San Luis Potos?, Av. Parque Chapultepec 1570, San Luis Potos?, 78210, Mexico
Type
Article
Source Title
Pharmaceuticals
ISSN
14248247
Year
2024
Volume
17
Issue
3
Open Access
All Open Access, Gold
Publisher
Multidisciplinary Digital Publishing Institute (MDPI)
DOI
10.3390/ph17030302
Abstract
Subunit vaccines stand as a leading approach to expanding the current portfolio of vaccines to fight against COVID-19, seeking not only to lower costs but to achieve long-term immunity against variants of concern and have the main attributes that could overcome the limitations of the current vaccines. Herein a chimeric protein targeting S1 and S2 epitopes, called LTp50, was designed as a convenient approach to induce humoral responses against SARS-CoV-2. LTp50 was produced in recombinant Escherichia coli using a conventional pET vector, recovering the expected antigen in the insoluble fraction. LTp50 was purified by chromatography (purity > 90%). The solubilization and refolding stages helped to obtain a stable protein amenable for vaccine formulation. LTp50 was adsorbed onto alum, resulting in a stable formulation whose immunogenic properties were assessed in BALB/c mice. Significant humoral responses against the S protein (BA.5 variant) were detected in mice subjected to three subcutaneous doses (10 ?g) of the LTp50/alum formulation. This study opens the path for the vaccine formulation optimization using additional adjuvants to advance in the development of a highly effective anti-COVID-19 vaccine directed against the antigenic regions of the S protein, which are less prone to mutations. ? 2024 by the authors.
Keyword
19 | built | chimeric antigen | COVID | humoral response | in adjuvant | linear epitopes
Industrial Classification
Knowledge Taxonomy Level 1
Knowledge Taxonomy Level 2
Knowledge Taxonomy Level 3
License
CC BY
Rights
Authors
Publication Source
WoS