2004
DOI: 10.1128/jvi.78.18.10034-10044.2004
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Discrimination among Rhinovirus Serotypes for a Variant ICAM-1 Receptor Molecule

Abstract: Kilifi contain one less salt bridge than between the viruses and ICAM-1. As HRV16 has fewer overall interactions with ICAM-1 than HRV14, the absence of this charge interaction has a greater impact on the binding of ICAM-1 Kilifi to HRV16 than to HRV14.

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Cited by 20 publications
(22 citation statements)
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References 60 publications
(81 reference statements)
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“…Studies on human rhinovirus (HRV) using two different HRV serotypes have shown varying adhesion phenotypes to ICAM-1 Reference and ICAM-1 Kilifi , and their association with varying clinical outcome [88]. A similar situation may occur in P. falciparum variants from the field as shown in this study and in laboratory lines [63] that exhibit differential adhesion abilities to all three ICAM-1 proteins.…”
Section: Discussionsupporting
confidence: 63%
“…Studies on human rhinovirus (HRV) using two different HRV serotypes have shown varying adhesion phenotypes to ICAM-1 Reference and ICAM-1 Kilifi , and their association with varying clinical outcome [88]. A similar situation may occur in P. falciparum variants from the field as shown in this study and in laboratory lines [63] that exhibit differential adhesion abilities to all three ICAM-1 proteins.…”
Section: Discussionsupporting
confidence: 63%
“…Although many different cellular factors have been identified as entry receptors, the visualization of picornavirus-receptor interactions at atomic or near-atomic resolution is still relatively rare, due in some cases to the inherent flexibility of the receptor binding portions. A number of enterovirus receptor complexes have been determined, including: PV with CD155 (9-11), major group HRV and CVA21 with intercellular adhesion molecule 1 (ICAM-1), minor group HRV with very-low-density lipoprotein receptor (VLDLR) (12)(13)(14)(15), and CVB3 with coxsackievirusadenovirus receptor (CAR) and decay-accelerating factor (DAF) Significance Seneca Valley virus (SVV) selectively infects and lyses neuroendocrine cancer cells, including small-cell lung cancer (SCLC) and pediatric neuroendocrine solid tumors, which are a major cause of morbidity and mortality. It is under development in clinical trials as an oncolytic agent against these tumors.…”
Section: Seneca Valley Virus (Svv)mentioning
confidence: 99%
“…Assignment of an RV to a given species is based on sequences of the VP4/VP2 or VP1 proteins (11). In most RVs, binding and fusion of the viral particle are mediated by attachment to ICAM-1 (12), which binds to a pocket groove of the VP-1 protein (13). Other subtypes of RVs bind to LDL receptor family receptors.…”
mentioning
confidence: 99%