Self-assembly of highly phosphorylated silaffins and their function in biosilica morphogenesis
Research output: Contribution to journal › Research article › Contributed › peer-review
Contributors
Abstract
Silaffins are uniquely modified peptides that have been implicated in the biogenesis of diatom biosilica. A method that avoids the harsh anhydrous hydrogen fluoride treatment commonly used to dissolve biosilica allows the extraction of silaffins in their native state. The native silaffins carry further posttranslational modifications in addition to their polyamine moieties. Each serine residue was phosphorylated, and this high level of phosphorylation is essential for biological activity. The zwitterionic structure of native silaffins enables the formation of supramolecular assemblies. Time-resolved analysis of silica morphogenesis in vitro detected a plastic silaffin-silica phase, which may represent a building material for diatom biosilica.
Details
Original language | English |
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Pages (from-to) | 584-586 |
Number of pages | 3 |
Journal | Science |
Volume | 298 |
Issue number | 5593 |
Publication status | Published - 18 Oct 2002 |
Peer-reviewed | Yes |
External IDs
PubMed | 12386330 |
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