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10.3390/v13050832

http://scihub22266oqcxt.onion/10.3390/v13050832
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34064525!8147968!34064525
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suck abstract from ncbi


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pmid34064525      Viruses 2021 ; 13 (5): ä
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  • Identification of the SHREK Family of Proteins as Broad-Spectrum Host Antiviral Factors #MMPMID34064525
  • Dabbagh D; He S; Hetrick B; Chilin L; Andalibi A; Wu Y
  • Viruses 2021[May]; 13 (5): ä PMID34064525show ga
  • Mucins and mucin-like molecules are highly glycosylated, high-molecular-weight cell surface proteins that possess a semi-rigid and highly extended extracellular domain. P-selectin glycoprotein ligand-1 (PSGL-1), a mucin-like glycoprotein, has recently been found to restrict HIV-1 infectivity through virion incorporation that sterically hinders virus particle attachment to target cells. Here, we report the identification of a family of antiviral cellular proteins, named the Surface-Hinged, Rigidly-Extended Killer (SHREK) family of virion inactivators (PSGL-1, CD43, TIM-1, CD34, PODXL1, PODXL2, CD164, MUC1, MUC4, and TMEM123) that share similar structural characteristics with PSGL-1. We demonstrate that SHREK proteins block HIV-1 infectivity by inhibiting virus particle attachment to target cells. In addition, we demonstrate that SHREK proteins are broad-spectrum host antiviral factors that block the infection of diverse viruses such as influenza A. Furthermore, we demonstrate that a subset of SHREKs also blocks the infectivity of a hybrid alphavirus-SARS-CoV-2 (Ha-CoV-2) pseudovirus. These results suggest that SHREK proteins may be a part of host innate immunity against enveloped viruses.
  • |*Virus Attachment[MESH]
  • |Animals[MESH]
  • |COVID-19/*immunology/virology[MESH]
  • |Dogs[MESH]
  • |HEK293 Cells[MESH]
  • |HIV Infections/*immunology[MESH]
  • |HIV-1/immunology[MESH]
  • |HeLa Cells[MESH]
  • |Host Microbial Interactions[MESH]
  • |Humans[MESH]
  • |Immunity, Innate[MESH]
  • |Madin Darby Canine Kidney Cells[MESH]
  • |Membrane Glycoproteins/*metabolism[MESH]
  • |Mucins/pharmacology[MESH]


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