Literature DB >> 32913137

Heparin-binding Peptides as Novel Therapies to Stop SARS-CoV-2 Cellular Entry and Infection.

Omid Tavassoly1, Farinaz Safavi2, Iman Tavassoly1.   

Abstract

Heparan sulfate proteoglycans (HSPGs) are cell surface receptors that are involved in the cellular uptake of pathologic amyloid proteins and viruses, including the novel coronavirus; severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Heparin and heparan sulfate antagonize the binding of these pathogens to HSPGs and stop their cellular internalization, but the anticoagulant effect of these agents has been limiting their use in the treatment of viral infections. Heparin-binding peptides (HBPs) are suitable nonanticoagulant agents that are capable of antagonizing binding of heparin-binding pathogens to HSPGs. Here, we review and discuss the use of HBPs as viral uptake inhibitors and will address their benefits and limitations to treat viral infections. Furthermore, we will discuss a variant of these peptides that is in the clinic and can be considered as a novel therapy in coronavirus disease 2019 (COVID-19) infection. SIGNIFICANCE STATEMENT: The need to discover treatment modalities for COVID-19 is a necessity, and therapeutic interventions such as heparin-binding peptides (HBPs), which are used for other cases, can be beneficial based on their mechanisms of actions. In this paper, we have discussed the application of HBPs as viral uptake inhibitors in COVID-19 and explained possible mechanisms of actions and the therapeutic effects. U.S. Government work not protected by U.S. copyright.

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Year:  2020        PMID: 32913137      PMCID: PMC7610036          DOI: 10.1124/molpharm.120.000098

Source DB:  PubMed          Journal:  Mol Pharmacol        ISSN: 0026-895X            Impact factor:   4.436


  79 in total

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Review 3.  Strategies to improve drug delivery across the blood-brain barrier.

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4.  Interaction of Zika Virus Envelope Protein with Glycosaminoglycans.

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Journal:  Biochemistry       Date:  2017-02-13       Impact factor: 3.162

5.  Human papillomavirus infection requires cell surface heparan sulfate.

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Journal:  J Virol       Date:  2001-02       Impact factor: 5.103

6.  Acidosis increases MHC class II-restricted presentation of a protein endowed with a pH-dependent heparan sulfate-binding ability.

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  13 in total

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Review 3.  Cardiovascular protective properties of oxytocin against COVID-19.

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Review 4.  Endothelial cells and SARS-CoV-2: An intimate relationship.

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6.  SARS-CoV-2 spike protein interactions with amyloidogenic proteins: Potential clues to neurodegeneration.

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7.  Brilacidin, a COVID-19 drug candidate, demonstrates broad-spectrum antiviral activity against human coronaviruses OC43, 229E, and NL63 through targeting both the virus and the host cell.

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9.  Decoding Clinical Biomarker Space of COVID-19: Exploring Matrix Factorization-based Feature Selection Methods.

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10.  The in vitro antiviral activity of lactoferrin against common human coronaviruses and SARS-CoV-2 is mediated by targeting the heparan sulfate co-receptor.

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