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41    INNOSC Theranostics and Pharmacological Sciences, 2022, Vol. 5, No. 2                     Das et al.
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           Figure 4. Protein-protein interaction of (A) angiotensin-converting enzyme 2 (ACE2) receptor with the S
           protein, (B) S protein-mHTCC complex with ACE2 receptor, and (C) S protein-N-carboxymethyl chitosan
           complex with ACE2 receptor.

           4. Discussion                                        unit  of mHTCC with the spike protein,  RBD of
                                                                the S protein and the ACE2 receptor. The protein-
           Chitosan derivatives have been reported to influence   protein  interaction  study revealed  the  binding
           inhibitors of various human pathogenic  viruses,     efficiency of mHTCC and the S protein complex
           including  influenza  virus,  HIV,  Newcastle  virus,   with  ACE2 receptor, indicating  that mHTCC
           human norovirus, murine virus, feline calicivirus,   inhibits the binding affinity of the S protein with
           hepatitis  C  virus,  Friend  murine  leukemia  helper   ACE 2 receptor. These findings are consistent with
           virus (F-MuLV), herpes simplex virus (HSV), pox      prior research.
           virus, and human coronavirus [20,30]. In the present    In a recent study by Malik et al. [31], trimethyl
           study, we focused on the usage of biodegradable      chitosan (TMC) was identified as a potent chitosan
           and biocompatible  chitosan and its derivatives,     derivative  with properties  such as high aqueous
           which exhibit  potent  inhibition  against  spike    solubility, stability  over  a  wide  range  of ionic
           proteins of coronaviruses. We thoroughly evaluated   conditions, and mucoadhesive properties, making
           the effect of molecular weight, configuration, and   it an effective adjuvant molecule. TMC was found
           DS  on  different  monomeric  and  oligomeric  units   to  induce  strong antibody  responses and  robust
           of chitosan derivatives  and their interaction  with   cell-mediated immunity. Alongside TMC, HTCC,
           the spike protein. Milewska et al. [17] reported a   a cationic chitosan derivative, has been proven to
           decline  in  viral  infection  rate  and  multiplication   be effective as an adjuvant when co-administered
           when employing HTCC, a polymeric derivative of       with  the  hepatitis  E  virus (HEV) recombinant
           chitosan, in the culture medium of human airway      polypeptide vaccine through the intramuscular
           epithelium  cell  lines.  HTCC  was  also  identified   route. Vaccination using HTCC as an adjuvant was
           as  a  broad-range  inhibitor  of  the  other  human   associated with an increase in serum HEV-specific
           coronaviruses in its polymeric form, with the DS     IgG  antibodies, splenocyte proliferation,  and the
           varying from 57% to 77% [18]. In our study, we       growth  of  CD4+  and  CD8+  T  lymphocytes,  and
           evaluated the interaction affinity of the monomeric   IFN-γ-secreting T lymphocytes in peripheral blood.

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