[NMR paper] A Combined NMR-Computational Study of the Interaction between Influenza Virus Hemagglutinin and Sialic Derivatives from Human and Avian Receptors on the Surface of Transfected Cells.
A Combined NMR-Computational Study of the Interaction between Influenza Virus Hemagglutinin and Sialic Derivatives from Human and Avian Receptors on the Surface of Transfected Cells.
Related ArticlesA Combined NMR-Computational Study of the Interaction between Influenza Virus Hemagglutinin and Sialic Derivatives from Human and Avian Receptors on the Surface of Transfected Cells.
Int J Mol Sci. 2018 Apr 24;19(5):
Authors: Vasile F, Panigada M, Siccardi A, Potenza D, Tiana G
Abstract
The development of small-molecule inhibitors of influenza virus Hemagglutinin could be relevant to the opposition of the diffusion of new pandemic viruses. In this work, we made use of Nuclear Magnetic Resonance (NMR) spectroscopy to study the interaction between two derivatives of sialic acid, Neu5Ac-α-(2,6)-Gal-β-(1?4)-GlcNAc and Neu5Ac-α-(2,3)-Gal-β-(1?4)-GlcNAc, and hemagglutinin directly expressed on the surface of recombinant human cells. We analyzed the interaction of these trisaccharides with 293T cells transfected with the H5 and H1 variants of hemagglutinin, which thus retain their native trimeric conformation in such a realistic environment. By exploiting the magnetization transfer between the protein and the ligand, we obtained evidence of the binding event, and identified the epitope. We analyzed the conformational features of the glycans with an approach combining NMR spectroscopy and data-driven molecular dynamics simulations, thus obtaining useful information for an efficient drug design.
[NMR paper] NMR interaction studies of Neu5Ac-?-(2,6)-Gal-?-(1-4)-GlcNAc with influenza-virus Hemagglutinin expressed in transfected human cells.
NMR interaction studies of Neu5Ac-?-(2,6)-Gal-?-(1-4)-GlcNAc with influenza-virus Hemagglutinin expressed in transfected human cells.
NMR interaction studies of Neu5Ac-?-(2,6)-Gal-?-(1-4)-GlcNAc with influenza-virus Hemagglutinin expressed in transfected human cells.
Glycobiology. 2017 Oct 26;:
Authors: Vasile F, Gubinelli F, Panigada M, Soprana E, Siccardi A, Potenza D
Abstract
The emergence of escape-mutants of Influenza Hemagglutinin following vaccination compels the yearly re-formulation of flu vaccines. Since binding the...
Researchers discover how the kissing disease virus hijacks human cells - EurekAlert (press release)
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Researchers discover how the kissing disease virus hijacks human cells
EurekAlert (press release)
Using cutting-edge nuclear magnetic resonance techniques at the University of Montreal facility for structural biology in the Department of Biochemistry and Molecular Medicine, the scientists studied how the EBNA2 protein of the EBV virus binds to one ...
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Researchers discover how the kissing disease virus hijacks human cells - EurekAlert (press release)
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nmrlearner
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04-10-2014 02:25 PM
Journal Highlight: NMR structures of fusion peptide from influenza hemagglutinin H3 subtype and its mutants
Journal Highlight: NMR structures of fusion peptide from influenza hemagglutinin H3 subtype and its mutants
http://www.spectroscopynow.com/common/images/thumbnails/14513e996b9.jpgThe structures of the influenza hemagglutinin H3-HAfp23 peptide and its mutants, G1S and G1V, in dodecylphosphatidyl choline micelles were studied by heteronuclear NMR spectroscopy to study the role of its amino acids in the fusion process.
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nmrlearner
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03-31-2014 10:16 AM
[NMR paper] pH-triggered, activated-state conformations of the influenza hemagglutinin fusion peptide revealed by NMR.
pH-triggered, activated-state conformations of the influenza hemagglutinin fusion peptide revealed by NMR.
http://www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--highwire.stanford.edu-icons-externalservices-pubmed-custom-pnas_full_free.gif http://www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--highwire.stanford.edu-icons-externalservices-pubmed-custom-pnas_full.gif http://www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--www.pubmedcentral.nih.gov-corehtml-pmc-pmcgifs-pubmed-pmc.gif Related Articles pH-triggered, activated-state conformations of the influenza hemagglutinin fusion...
nmrlearner
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02-07-2013 10:31 PM
[NMR paper] Detection of closed influenza virus hemagglutinin fusion peptide structures in membranes by backbone (13)CO- (15)N rotational-echo double-resonance solid-state NMR.
Detection of closed influenza virus hemagglutinin fusion peptide structures in membranes by backbone (13)CO- (15)N rotational-echo double-resonance solid-state NMR.
http://www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--production.springer.de-OnlineResources-Logos-springerlink.gif Related Articles Detection of closed influenza virus hemagglutinin fusion peptide structures in membranes by backbone (13)CO- (15)N rotational-echo double-resonance solid-state NMR.
J Biomol NMR. 2013 Jan 18;
Authors: Ghosh U, Xie L, Weliky DP
Abstract...
nmrlearner
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02-03-2013 10:19 AM
[NMR paper] NMR mapping of the HIV-1 Tat interaction surface of the KIX domain of the human coact
NMR mapping of the HIV-1 Tat interaction surface of the KIX domain of the human coactivator CBP.
Related Articles NMR mapping of the HIV-1 Tat interaction surface of the KIX domain of the human coactivator CBP.
Biochemistry. 2004 Feb 3;43(4):904-8
Authors: Vendel AC, Lumb KJ
Tat is required for the expression of the HIV-1 genome. HIV-1 Tat interacts with the human transcriptional coactivator and acetyltransferase CREB-binding protein (CBP) via the KIX domain of CBP. Chemical shift perturbation mapping with nuclear magnetic resonance...
nmrlearner
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11-24-2010 09:25 PM
[NMR paper] 1H NMR studies on the interaction of beta-carboline derivatives with human serum albu
1H NMR studies on the interaction of beta-carboline derivatives with human serum albumin.
Related Articles 1H NMR studies on the interaction of beta-carboline derivatives with human serum albumin.
J Magn Reson. 1998 Feb;130(2):281-6
Authors: Veglia G, Delfini M, Giudice MR, Gaggelli E, Valensin G
1H NMR studies were performed on two beta-carboline derivatives interacting with human serum albumin. The spin-lattice relaxation rates of the two derivatives, having side chains of different length and polarity, were used to demonstrate a diverse...