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Bioorganic/inorganic hybrid composition of sponge spicules: Matrix of the giant spicules and of the comitalia of the deep sea hexactinellid Monorhaphis

  • Werner E.G. Müller*
  • , Xiaohong Wang
  • , Klaus Kropf
  • , Hiroshi Ushijima
  • , Werner Geurtsen
  • , Carsten Eckert
  • , Muhammad Nawaz Tahir
  • , Wolfgang Tremel
  • , Alexandra Boreiko
  • , Ute Schloßmacher
  • , Jinhe Li
  • , Heinz C. Schröder
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

83 Scopus citations

Abstract

The giant basal spicules of the siliceous sponges Monorhaphis chuni and Monorhaphis intermedia (Hexactinellida) represent the largest biosilica structures on earth (up to 3 m long). Here we describe the construction (lamellar organization) of these spicules and of the comitalia and highlight their organic matrix in order to understand their mechanical properties. The spicules display three distinct regions built of biosilica: (i) the outer lamellar zone (radius: >300 μm), (ii) the bulky axial cylinder (radius: <75 μm), and (iii) the central axial canal (diameter: <2 μm) with its organic axial filament. The spicules are loosely covered with a collagen net which is regularly perforated by 7-10 μm large holes; the net can be silicified. The silica layers forming the lamellar zone are ≈5 μm thick; the central axial cylinder appears to be composed of almost solid silica which becomes porous after etching with hydrofluoric acid (HF). Dissolution of a complete spicule discloses its complex structure with distinct lamellae in the outer zone (lamellar coating) and a more resistant central part (axial barrel). Rapidly after the release of the organic coating from the lamellar zone the protein layers disintegrate to form irregular clumps/aggregates. In contrast, the proteinaceous axial barrel, hidden in the siliceous axial cylinder, is set up by rope-like filaments. Biochemical analysis revealed that the (dominant) molecule of the lamellar coating is a 27-kDa protein which displays catalytic, proteolytic activity. High resolution electron microscopic analysis showed that this protein is arranged within the lamellae and stabilizes these surfaces by palisade-like pillars. The mechanical behavior of the spicules was analyzed by a 3-point bending assay, coupled with scanning electron microscopy. The load-extension curve of the spicule shows a biphasic breakage/cracking pattern. The outer lamellar zone cracks in several distinct steps showing high resistance in concert with comparably low elasticity, while the axial cylinder breaks with high elasticity and lower stiffness. The complex bioorganic/inorganic hybrid composition and structure of the Monorhaphis spicules might provide the blueprint for the synthesis of bio-inspired material, with unusual mechanical properties (strength, stiffness) without losing the exceptional properties of optical transmission.

Original languageEnglish
Pages (from-to)188-203
Number of pages16
JournalJournal of Structural Biology
Volume161
Issue number2
DOIs
StatePublished - Feb 2008
Externally publishedYes

Bibliographical note

Funding Information:
This work was supported by grants from the European Commission, the Deutsche Forschungsgemeinschaft, the Bundesministerium für Bildung und Forschung Germany (Project: Center of Excellence BIOTECmarin), the National Natural Science Foundation of China (No. 50402023) and the International Human Frontier Science Program.

Keywords

  • Elasticity
  • Hybrid composite material
  • Monorhaphis
  • Silicatein
  • Spicules
  • Sponges

ASJC Scopus subject areas

  • Structural Biology

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