Matches in SemOpenAlex for { <https://semopenalex.org/work/W2155016049> ?p ?o ?g. }
- W2155016049 endingPage "9114" @default.
- W2155016049 startingPage "9106" @default.
- W2155016049 abstract "Cell surface heparan sulfate (HS) serves as an initial receptor for many different viruses, including herpes simplex virus types 1 and 2 (HSV-1 and 2, respectively). Glycoproteins C and B (gC and gB) are the major components of the viral envelope that mediate binding to HS. In this study, purified gB and gC homologous proteins as well as purified HSV-1 and HSV-2 virions were compared for the ability to bind isolated HS receptor molecules. HSV-1 gC and HSV-2 gC bound comparable amounts of HS. Similarly, HSV-1 gB and its HSV-2 counterpart showed no difference in the HS-binding capabilities. Despite the similar HS-binding potentials of gB and gC homologs, HSV-1 virions bound more HS than HSV-2 particles. Purified gC and gB proteins differed with respect to sensitivity of their interaction with HS to increased concentrations of sodium chloride in the order gB-2 > gB-1 > gC-1 > gC-2. The corresponding pattern for binding of whole HSV virions to cells in the presence of increased ionic strength of the medium was HSV-2 gC-neg1 > HSV-1 gC(-)39 > HSV-1 KOS 321 > HSV-2 333. These results relate the HS-binding activities of individual glycoproteins with the cell-binding abilities of whole virus particles. In addition, these data suggest a greater contribution of electrostatic forces for binding of gB proteins and gC-negative mutants compared with binding of gC homologs and wild-type HSV strains. Binding of wild-type HSV-2 virions was the least sensitive to increased ionic strength of the medium, suggesting that the less extensive binding of HS molecules by HSV-2 than by HSV-1 can be compensated for by a relatively weak contribution of electrostatic forces to the binding. Furthermore, gB and gC homologs exhibited different patterns of sensitivity of binding to cells to inhibition with selectively N-, 2-O-, and 6-O-desulfated heparin compounds. The O-sulfate groups of heparin were found to be more important for interaction with gB-1 than gB-2. These results indicate that HSV-1 and HSV-2 differ in their interaction with HS." @default.
- W2155016049 created "2016-06-24" @default.
- W2155016049 creator A5005392535 @default.
- W2155016049 creator A5035772207 @default.
- W2155016049 creator A5055221957 @default.
- W2155016049 creator A5073376985 @default.
- W2155016049 date "2000-10-01" @default.
- W2155016049 modified "2023-10-13" @default.
- W2155016049 title "Herpes Simplex Virus Types 1 and 2 Differ in Their Interaction with Heparan Sulfate" @default.
- W2155016049 cites W1484618820 @default.
- W2155016049 cites W1485135772 @default.
- W2155016049 cites W1504702403 @default.
- W2155016049 cites W1565758785 @default.
- W2155016049 cites W1566122361 @default.
- W2155016049 cites W1570853101 @default.
- W2155016049 cites W1572560385 @default.
- W2155016049 cites W1579878633 @default.
- W2155016049 cites W1589735909 @default.
- W2155016049 cites W158986509 @default.
- W2155016049 cites W1594175085 @default.
- W2155016049 cites W1608390571 @default.
- W2155016049 cites W1768619547 @default.
- W2155016049 cites W1840760750 @default.
- W2155016049 cites W1867634595 @default.
- W2155016049 cites W1890282385 @default.
- W2155016049 cites W1912291173 @default.
- W2155016049 cites W1915870046 @default.
- W2155016049 cites W1923243377 @default.
- W2155016049 cites W1927596245 @default.
- W2155016049 cites W1964631389 @default.
- W2155016049 cites W1971247590 @default.
- W2155016049 cites W1976172519 @default.
- W2155016049 cites W1984624532 @default.
- W2155016049 cites W1992115589 @default.
- W2155016049 cites W1992223490 @default.
- W2155016049 cites W1999466649 @default.
- W2155016049 cites W2001371234 @default.
- W2155016049 cites W2003326907 @default.
- W2155016049 cites W2020206304 @default.
- W2155016049 cites W2020338189 @default.
- W2155016049 cites W2030324405 @default.
- W2155016049 cites W2031606209 @default.
- W2155016049 cites W2050082215 @default.
- W2155016049 cites W2065628860 @default.
- W2155016049 cites W2070657108 @default.
- W2155016049 cites W2077707212 @default.
- W2155016049 cites W2095299808 @default.
- W2155016049 cites W2102046260 @default.
- W2155016049 cites W2102834112 @default.
- W2155016049 cites W2113394330 @default.
- W2155016049 cites W2124222169 @default.
- W2155016049 cites W2124432186 @default.
- W2155016049 cites W2127288704 @default.
- W2155016049 cites W2142862392 @default.
- W2155016049 cites W2143783595 @default.
- W2155016049 cites W2144612442 @default.
- W2155016049 cites W2153172339 @default.
- W2155016049 cites W2158981482 @default.
- W2155016049 cites W2159815530 @default.
- W2155016049 cites W2168292685 @default.
- W2155016049 cites W2312617763 @default.
- W2155016049 doi "https://doi.org/10.1128/jvi.74.19.9106-9114.2000" @default.
- W2155016049 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/102109" @default.
- W2155016049 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/10982357" @default.
- W2155016049 hasPublicationYear "2000" @default.
- W2155016049 type Work @default.
- W2155016049 sameAs 2155016049 @default.
- W2155016049 citedByCount "127" @default.
- W2155016049 countsByYear W21550160492012 @default.
- W2155016049 countsByYear W21550160492013 @default.
- W2155016049 countsByYear W21550160492014 @default.
- W2155016049 countsByYear W21550160492015 @default.
- W2155016049 countsByYear W21550160492017 @default.
- W2155016049 countsByYear W21550160492018 @default.
- W2155016049 countsByYear W21550160492019 @default.
- W2155016049 countsByYear W21550160492020 @default.
- W2155016049 countsByYear W21550160492021 @default.
- W2155016049 countsByYear W21550160492022 @default.
- W2155016049 countsByYear W21550160492023 @default.
- W2155016049 crossrefType "journal-article" @default.
- W2155016049 hasAuthorship W2155016049A5005392535 @default.
- W2155016049 hasAuthorship W2155016049A5035772207 @default.
- W2155016049 hasAuthorship W2155016049A5055221957 @default.
- W2155016049 hasAuthorship W2155016049A5073376985 @default.
- W2155016049 hasBestOaLocation W21550160491 @default.
- W2155016049 hasConcept C104317684 @default.
- W2155016049 hasConcept C108625454 @default.
- W2155016049 hasConcept C143065580 @default.
- W2155016049 hasConcept C1491633281 @default.
- W2155016049 hasConcept C153911025 @default.
- W2155016049 hasConcept C159047783 @default.
- W2155016049 hasConcept C170493617 @default.
- W2155016049 hasConcept C2522874641 @default.
- W2155016049 hasConcept C2778041096 @default.
- W2155016049 hasConcept C2781196997 @default.
- W2155016049 hasConcept C55493867 @default.
- W2155016049 hasConcept C86803240 @default.
- W2155016049 hasConceptScore W2155016049C104317684 @default.