Pregled bibliografske jedinice broj: 935916
Polysialic acid is a cellular receptor for human adenovirus 52
Polysialic acid is a cellular receptor for human adenovirus 52 // Proceedings of the National Academy of Sciences of the United States of America, 115 (2018), 18; E4264-E4273 doi:10.1073/pnas.1716900115 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 935916 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Polysialic acid is a cellular receptor for human adenovirus 52
Autori
Lenman, Annasara ; Liaci, A. Manuel ; Liu, Yan ; Frängsmyr, Lars ; Frank, Martin ; Blaum, Bärbel S. ; Chai, Wengang ; Podgorski, Iva I. ; Harrach, Balázs ; Benkő, Mária ; Feizi, Ten ; Stehle, Thilo ; Arnberg, Niklas
Izvornik
Proceedings of the National Academy of Sciences of the United States of America (0027-8424) 115
(2018), 18;
E4264-E4273
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
human adenovirus ; short fiber ; polysialic acid ; glycan receptor ; glycan microarray
Sažetak
Human adenovirus 52 (HAdV-52) is one of only three known HAdVs equipped with both a long and a short fiber protein. While the long fiber binds to the coxsackie and adenovirus receptor, the function of the short fiber in the virus life cycle is poorly understood. Here, we show, by glycan microarray analysis and cellular studies, that the short fiber knob (SFK) of HAdV-52 recognizes long chains of α-2, 8-linked polysialic acid (polySia), a large posttranslational modification of selected carrier proteins, and that HAdV-52 can use polySia as a receptor on target cells. X-ray crystallography, NMR, molecular dynamics simulation, and structure- guided mutagenesis of the SFK reveal that the nonreducing, terminal sialic acid of polySia engages the protein with direct contacts, and that specificity for polySia is achieved through subtle, transient electrostatic interactions with additional sialic acid residues. In this study, we present a previously unrecognized role for polySia as a cellular receptor for a human viral pathogen. Our detailed analysis of the determinants of specificity for this interaction has general implications for protein–carbohydrate interactions, particularly concerning highly charged glycan structures, and provides interesting dimensions on the biology and evolution of members of Human mastadenovirus G.
Izvorni jezik
Engleski
Znanstvena područja
Biologija
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE
- EconLit
- Nature Index