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1.
Molecules ; 29(7)2024 Apr 01.
Article in English | MEDLINE | ID: mdl-38611856

ABSTRACT

SARS-CoV-2 is the virus responsible for a respiratory disease called COVID-19 that devastated global public health. Since 2020, there has been an intense effort by the scientific community to develop safe and effective prophylactic and therapeutic agents against this disease. In this context, peptides have emerged as an alternative for inhibiting the causative agent. However, designing peptides that bind efficiently is still an open challenge. Here, we show an algorithm for peptide engineering. Our strategy consists of starting with a peptide whose structure is similar to the interaction region of the human ACE2 protein with the SPIKE protein, which is important for SARS-COV-2 infection. Our methodology is based on a genetic algorithm performing systematic steps of random mutation, protein-peptide docking (using the PyRosetta library) and selecting the best-optimized peptides based on the contacts made at the peptide-protein interface. We performed three case studies to evaluate the tool parameters and compared our results with proposals presented in the literature. Additionally, we performed molecular dynamics (MD) simulations (three systems, 200 ns each) to probe whether our suggested peptides could interact with the spike protein. Our results suggest that our methodology could be a good strategy for designing peptides.


Subject(s)
COVID-19 , Spike Glycoprotein, Coronavirus , Humans , SARS-CoV-2 , Peptides/pharmacology
2.
Methods Mol Biol ; 1352: 263-77, 2016.
Article in English | MEDLINE | ID: mdl-26490482

ABSTRACT

Peptide microarrays have become increasingly more affordable in recent years with the SPOT technique being one of the most frequently used methods for synthesis and screening of peptides in arrays. Here, a protocol is presented for the identification of the amino acid sites involved in the conversion of human IgG to IgE response during the passive administration of therapeutic, anti-snake venom sera. Similarly, the minimal region of both the IgG and IgE binding epitopes, important for its interaction with ligand, were identified. As the ratio of concentrations for IgG to IgE in human serum is 1:10,000, also presented is a reproductive protocol of chemiluminescence-scanning for the detection of both immunoglobulins.


Subject(s)
Epitope Mapping/methods , Immunoglobulin E/immunology , Peptides/chemical synthesis , Peptides/immunology , Protein Array Analysis/methods , Acetylation , Animals , Cellulose/chemistry , Chemistry Techniques, Synthetic , Humans , Immunoglobulin G/immunology , Membranes, Artificial , Peptides/chemistry
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