Sally Furniss
Well-known member
The relevance of salt bridges for the stability of the influenza virus hemagglutinin
<nobr>P. Sivaramakrishna Rachakonda<sup>*</sup></nobr>, <nobr>Michael Veit<sup>
</sup></nobr>, <nobr>Thomas Korte<sup>*</sup></nobr>, <nobr>Kai Ludwig<sup>
</sup></nobr>, <nobr>Christoph Böttcher<sup>
</sup></nobr>, <nobr>Qiang Huang<sup>
</sup></nobr>, <nobr>Michael F. G. Schmidt<sup>
</sup></nobr> and <nobr>Andreas Herrmann<sup>*</sup><sup>,1</sup></nobr> [SIZE=-1] <sup>*</sup> Humboldt-Universität zu Berlin, Mathematisch-Naturwissenschaftliche Fakultät I, Institut für Biologie/Biophysik, Berlin, Germany;
<sup>
</sup> Institut für Immunologie und Molekularbiologie, Vet.-Med. Fakultät, Freie Universität Berlin, Berlin, Germany;
<sup>
</sup> Forschungszentrum für Elektronenmikroskopie, Freie Universität Berlin, Berlin, Germany; and
<sup>
</sup> State Key Laboratory of Genetic Engineering, School of Life Sciences, Fudan University, Shanghai, China [/SIZE]
[SIZE=-1]<sup>1</sup>Correspondence: Humboldt-Universität zu Berlin, Mathematisch-Naturwissenschaftliche Fakultät I, Institut für Biologie/Biophysik, Invalidenstr. 43, D-10115 Berlin, Germany. E-mail: andreas.herrmann@rz.hu-berlin.de
<script type="text/javascript"><!-- var u = "andreas.herrmann", d = "rz.hu-berlin.de"; document.getElementById("em0").innerHTML = '<a href="mailto:' + u + '@' + d + '">' + u + '@' + d + '<\/a>'//--></script>[/SIZE]
<!-- ABS --> Hemagglutinin (HA) of influenza virus undergoes an irreversible<sup> </sup>conformational change at acidic pH, mediating viral fusion with<sup> </sup>the host endosomal membrane. To unravel the molecular basis<sup> </sup>of the pH-dependent stability of HA, we demonstrate by mutagenesis<sup> </sup>of the prototype HA of virus strain X31 (H3 subtype) that salt<sup> </sup>bridges, especially a tetrad salt bridge within the monomers,<sup> </sup>are crucial for folding and stability of the trimeric ectodomain.<sup> </sup>This complex (tetrad) salt bridge is highly conserved among<sup> </sup>influenza virus subtypes. Introducing additional sites of electrostatic<sup> </sup>attraction between monomers in the distal region enhanced the<sup> </sup>stability of ectodomain at low pH mimicking the natural variant<sup> </sup>H2 subtype. We propose that distinct salt bridges in the distal<sup> </sup>domain may contribute to the enhanced stability of HA of natural<sup> </sup>virus variants. This hypothesis may provide clues to understanding<sup> </sup>adaptations of virus strains (for example, avian influenza viruses)<sup> </sup>in order to preserve stability of the protein in the host-specific<sup> </sup>environment.
—Rachakonda, P. S., Veit, M., Korte, T., Ludwig,<sup> </sup>K., Böttcher, C., Huang, Q., Schmidt, M. F. G., Herrmann,<sup> </sup>A. The relevance of salt bridges for the stability of the influenza<sup> </sup>virus hemagglutinin.
http://www.fasebj.org/cgi/content/abstract/21/4/995
<nobr>P. Sivaramakrishna Rachakonda<sup>*</sup></nobr>, <nobr>Michael Veit<sup>
<sup>
<sup>
<sup>
[SIZE=-1]<sup>1</sup>Correspondence: Humboldt-Universität zu Berlin, Mathematisch-Naturwissenschaftliche Fakultät I, Institut für Biologie/Biophysik, Invalidenstr. 43, D-10115 Berlin, Germany. E-mail: andreas.herrmann@rz.hu-berlin.de
<script type="text/javascript"><!-- var u = "andreas.herrmann", d = "rz.hu-berlin.de"; document.getElementById("em0").innerHTML = '<a href="mailto:' + u + '@' + d + '">' + u + '@' + d + '<\/a>'//--></script>[/SIZE]
<!-- ABS --> Hemagglutinin (HA) of influenza virus undergoes an irreversible<sup> </sup>conformational change at acidic pH, mediating viral fusion with<sup> </sup>the host endosomal membrane. To unravel the molecular basis<sup> </sup>of the pH-dependent stability of HA, we demonstrate by mutagenesis<sup> </sup>of the prototype HA of virus strain X31 (H3 subtype) that salt<sup> </sup>bridges, especially a tetrad salt bridge within the monomers,<sup> </sup>are crucial for folding and stability of the trimeric ectodomain.<sup> </sup>This complex (tetrad) salt bridge is highly conserved among<sup> </sup>influenza virus subtypes. Introducing additional sites of electrostatic<sup> </sup>attraction between monomers in the distal region enhanced the<sup> </sup>stability of ectodomain at low pH mimicking the natural variant<sup> </sup>H2 subtype. We propose that distinct salt bridges in the distal<sup> </sup>domain may contribute to the enhanced stability of HA of natural<sup> </sup>virus variants. This hypothesis may provide clues to understanding<sup> </sup>adaptations of virus strains (for example, avian influenza viruses)<sup> </sup>in order to preserve stability of the protein in the host-specific<sup> </sup>environment.
—Rachakonda, P. S., Veit, M., Korte, T., Ludwig,<sup> </sup>K., Böttcher, C., Huang, Q., Schmidt, M. F. G., Herrmann,<sup> </sup>A. The relevance of salt bridges for the stability of the influenza<sup> </sup>virus hemagglutinin.
http://www.fasebj.org/cgi/content/abstract/21/4/995