The schematic representation of multiepitope-based vaccine constructs (V1 and V2).

<p>The V1 (A) and V2 (B) containing adjuvants, epitopes, and linkers were depicted in different color codes.</p>

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Bibliographic Details
Main Author:	Rehana Parvin (841451) (author)
Other Authors:	Md. Habib Ullah Masum (13527469) (author), Homaira Pervin Heema (20714921) (author), Aklima Akter (5130614) (author), Mohammad Alamgir Hossain (20714924) (author), A. M. A. M. Zonaed Siddiki (8996447) (author)
Published:	2025
Subjects:	Microbiology Biotechnology Immunology Cancer Infectious Diseases Biological Sciences not elsewhere classified virtual physiological system significant binding affinity several computational platforms gbsa analyses confirmed following codon optimization employed computational approaches 28a (+) plasmid average gc content designed vaccine candidate potent ag5 antigen natural killer cell div >< p based vaccine using based vaccine grand average ag5 protein vaccine ’ tertiary structure successfully expressed structurally stable structural stability silico </ severe implications potent epitopes increased ifn immune responses highly soluble future preclinical findings highlight echinococcus </ e </ docked complexes coli </ cell derived cai value animal health also found 433 ). 34 %) 2 levels
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