Elise Hennebert

Polyphosphoprotein-Containing Marine Adhesives

Protein phosphorylation is an important regulator of both cellular and extracellular events. Recently, protein phosphorylation has also emerged as an important process in biological adhesives. During the last decade, Herbert Waite and his group have indeed characterized several polyphosphoproteins from the adhesive secretions of two different marine organisms, mussels and tube-building worms. This suggests the possibility that polyphosphoproteins could be important components of several bioadhesives and may, therefore, be widely distributed throughout the animal kingdom. Many amino acids can be targets for phosphorylation but only phosphoserine (pSer) has been detected to date in marine adhesive proteins. We investigated whether monoclonal antibodies directed against pSer could be used to specifically label polyphosphoproteins in marine adhesives. Antibodies were applied on histological sections through the foot of the mussel Mytilus edulis and through the building organ of the tube-worm Sabellaria alveolata. In both cases, anti-pSer binding was detected in the adhesive glands (phenol gland and cement gland, respectively). However, the intensity of the immunolabeling was different between the two species, being weak in the former and strong in the latter. With the use of these antibodies, a new pSer-rich bioadhesive has been detected in Cuvierian tubules, the sticky defense organs of sea cucumbers. Immunoblots and amino acid analyses confirmed the presence of polyphosphoproteins in the adhesive secretion of the Cuvierian tubules from three species of sea cucumber. These findings bring to three the number of animal groups in which adhesive processes involve polyphosphoproteins and raise interesting questions about the convergent evolution of these adhesives.

Micro- and nanostructure of the adhesive material secreted by the tube feet of the sea star Asterias rubens

To attach to underwater surfaces, sea stars rely on adhesive secretions produced by specialised organs, the tube feet. Adhesion is temporary and tube feet can also voluntarily become detached. The adhesive material is produced by two types of adhesive secretory cells located in the epidermis of the tube foot disc, and is deposited between the disc surface and the substratum. After detachment, this material remains on the substratum as a footprint. Using LM, SEM, and AFM, we described the fine structure of footprints deposited on various substrata by individuals of Asterias rubens. Ultrastructure of the adhesive layer of attached tube feet was also investigated using TEM. Whatever the method used, the adhesive material appeared as made up of globular nanostructures forming a meshwork deposited on a thin homogeneous film. This appearance did not differ according to whether the footprints were fixed or not, and whether they were observed hydrated or dry. TEM observations suggest that type 2 adhesive cells would be responsible for the release of the material constituting the homogeneous film whereas type 1 adhesive cells would produce the material forming the meshwork. This reticulated pattern would originate from the arrangement of the adhesive cell secretory pores on the disc surface.

Sea star tenacity mediated by a protein that fragments, then aggregates

Significance Sea stars are emblematic of the seashore. Despite this, their ability to pry open mussels and attach strongly but temporarily to rocks in their environments are poorly understood. Here we report, to our knowledge, the first sequence of a protein, Sea star footprint protein 1 (Sfp1), a primary constituent of the adhesive footprints secreted by sea star tube feet. Sfp1 is unusually large and complex compared with other marine adhesive proteins such as those of mussels. It is translated from a single mRNA and then fragmented into four subunits, which display specific domains that mediate interactions with other proteins present in the adhesive material and on the tube foot surface. After secretion, Sfp1 forms a structural scaffold and appears to provide footprints with cohesion. Sea stars adhere firmly but temporarily to various substrata as a result of underwater efficient adhesive secretions released by their tube feet. Previous studies showed that this material is mainly made up of proteins, which play a key role in its adhesiveness and cohesiveness. Recently, we solubilized the majority of these proteins and obtained 43 de novo-generated peptide sequences by tandem MS. Here, one of these sequences served to recover the full-length sequence of Sea star footprint protein 1 (Sfp1), by RT-PCR and tube foot transcriptome analysis. Sfp1, a large protein of 3,853 aa, is the second most abundant constituent of the secreted adhesive. By using MS and Western blot analyses, we showed that Sfp1 is translated from a single mRNA and then cleaved into four subunits linked together by disulphide bridges in tube foot adhesive cells. The four subunits display specific protein-, carbohydrate-, and metal-binding domains. Immunohistochemistry and immunocytochemistry located Sfp1 in granules stockpiled by one of the two types of adhesive cells responsible for the secretion of the adhesive material. We also demonstrated that Sfp1 makes up the structural scaffold of the adhesive footprint that remains on the substratum after tube foot detachment. Taken together, the results suggest that Sfp1 is a major structural protein involved in footprint cohesion and possibly in adhesive interactions with the tube foot surface. In recombinant form, it could be used for the design of novel sea star-inspired biomaterials.

Characterisation of the Carbohydrate Fraction of the Temporary Adhesive Secreted by the Tube Feet of the Sea Star Asterias rubens

In sea stars, adhesion takes place at the level of a multitude of small appendages, the tube feet. It involves the secretion of an adhesive material which, after tube foot detachment, remains on the substratum as a footprint. It was previously reported that the two main organic components of this material are proteins and carbohydrates. The carbohydrate moiety of the adhesive secretion of Asterias rubens was investigated using a set of 16 lectins which were used on sections through tube feet, on footprints, and on the proteins extracted from these footprints. After gel electrophoresis, these proteins separate into eight protein bands which were named sea star footprint proteins (Sfps). Eleven lectins label the tube foot epidermis at the level of the adhesive cells, four react with footprints, and eight with two of the extracted footprint proteins, which are therefore classified as glycoproteins. Sfp-290 appears to bear mostly N-linked oligosaccharides and Sfp-210 principally O-linked oligosaccharides. The outer chains of both glycoproteins enclose galactose, N-acetylgalactosamine, fucose, and sialic acid residues. Another part of the carbohydrate fraction of the footprints would be in the form of larger molecules, such as sialylated proteoglycans. These two types of glycoconjugates are presumably key components of the sea star temporary adhesive providing both cohesive and adhesive contributions through electrostatic interactions by the polar and hydrogen-bonding functional groups of their glycan chains.

Characterization of the protein fraction of the temporary adhesive secreted by the tube feet of the sea star Asterias rubens

Sea stars are able to make firm but temporary attachments to various substrata by secretions released by their tube feet. After tube foot detachment, the adhesive secretions remain on the substratum as a footprint. Proteins presumably play a key role in sea star adhesion, as evidenced by the removal of footprints from surfaces after a treatment with trypsin. However, until now, characterisation was hampered by their high insolubility. In this study, a non-hydrolytic method was used to render most of the proteins constituting the adhesive footprints soluble. After analysis by SDS-PAGE, the proteins separated into about 25 bands, which ranged from 25 to 450 kDa in apparent molecular weight. Using mass spectrometry and a homology-database search, it was shown that several of the proteins are known intracellular proteins, presumably resulting from contamination of footprint material with tube foot epidermal cells. However, 11 protein bands, comprising the most abundant proteins, were not identified and might correspond to novel adhesive proteins. They were named ‘Sea star footprint proteins’ (Sfps). Tandem mass spectrometry analysis of the protein bands yielded 43 de novo-generated peptide sequences. Most of them were shared by several, if not all, Sfps. Polyclonal antibodies were raised against one of the peptides (HEASGEYYR from Sfp-115) and were used in immunoblotting. They specifically labelled Sfp-115 and other bands with lower apparent molecular weights. The different results suggest that all Sfps might belong to a single family of related proteins sharing similar motifs or, alternatively, they are the products of polymerization and/or degradation processes.

Experimental strategies for the identification and characterization of adhesive proteins in animals: a review

Adhesive secretions occur in both aquatic and terrestrial animals, in which they perform diverse functions. Biological adhesives can therefore be remarkably complex and involve a large range of components with different functions and interactions. However, being mainly protein based, biological adhesives can be characterized by classical molecular methods. This review compiles experimental strategies that were successfully used to identify, characterize and obtain the full-length sequence of adhesive proteins from nine biological models: echinoderms, barnacles, tubeworms, mussels, sticklebacks, slugs, velvet worms, spiders and ticks. A brief description and practical examples are given for a variety of tools used to study adhesive molecules at different levels from genes to secreted proteins. In most studies, proteins, extracted from secreted materials or from adhesive organs, are analysed for the presence of post-translational modifications and submitted to peptide sequencing. The peptide sequences are then used directly for a BLAST search in genomic or transcriptomic databases, or to design degenerate primers to perform RT-PCR, both allowing the recovery of the sequence of the cDNA coding for the investigated protein. These sequences can then be used for functional validation and recombinant production. In recent years, the dual proteomic and transcriptomic approach has emerged as the best way leading to the identification of novel adhesive proteins and retrieval of their complete sequences.

An integrated transcriptomic and proteomic analysis of sea star epidermal secretions identifies proteins involved in defense and adhesion

Sea stars rely on epidermal secretions to cope with their benthic life. Their integument produces a mucus, which represents the first barrier against invaders; and their tube feet produce adhesive secretions to pry open mussels and attach strongly but temporarily to rocks. In this study, we combined high-throughput sequencing of expressed mRNA and mass-spectrometry-based identification of proteins to establish the first proteome of mucous and adhesive secretions from the sea star Asterias rubens. We show that the two secretions differ significantly, the major adhesive proteins being only present in trace amounts in the mucus secretion. Except for 41 proteins which were present in both secretions, a total of 34 and 244 proteins were identified as specific of adhesive secretions and mucus, respectively. We discuss the role of some of these proteins in the adhesion of sea stars as well as in their protection against oxygen reactive species and microorganisms. In addition, 58% of the proteins identified in adhesive secretions did not present significant similarity to other known proteins, revealing a list of potential novel sea star adhesive proteins uncharacterized so far. The panel of proteins identified in this study offers unprecedented opportunities for the development of sea star-inspired biomimetic materials.

The Echinoderm Tube Foot and its Role in Temporary Underwater Adhesion

Adhesion (attachment with adhesive secretions) is a way of life in the sea (Waite, 1983). Indeed, representatives of bacteria, protoctists (including macroalgae), and all animal phyla, living in the sea attach to natural or artificial surfaces. Adhesion ability is particularly developed and diversified in invertebrates, which adhere during their larval and adult life (Walker, 1987; Smith and Callow, 2006). It is involved in various functions such as the handling of food, the building of tubes or burrowing and, especially, the attachment to the substratum (Walker, 1987; Tyler, 1988; Whittington and Cribb, 2001; Flammang et al, 2005). Indeed, seawater, being a dense medium, denies gravity to hold organisms to the bottom. Thus, to withstand the hydrodynamic forces, marine organisms rely on specialised adhesive mechanisms.

Modification of the Adhesive Properties of Silicone-Based Coatings by Block Copolymers

The improvement of the (bio)adhesive properties of elastomeric polydimethylsiloxane (PDMS) coatings is reported. This is achieved by a surface modification consisting of the incorporation of block copolymers containing a PDMS block and a poly(2-(dimethylamino)ethyl methacrylate) (PDMAEMA) block in a PDMS matrix, followed by matrix cross-linking and immersion of the obtained materials in water. Contact angle measurements (CA), X-ray photoelectron spectroscopy (XPS), and atomic force microscopy (AFM) showed the presence of the PDMAEMA block at the surface, drastic morphology changes, and improved adhesion properties after immersion in water. Finally, underwater bioadhesion tests show that mussels adhere only to block copolymer-filled coatings and after immersion in water, i.e., when the PDMAEMA blocks have been brought to the coating surface. These observations highlight the significant role of hydrophilic groups in the surface modification of silicone coatings.

Evaluation of the different forces brought into play during tube foot activities in sea stars

SUMMARY Sea star tube feet consist of an enlarged and flattened distal extremity (the disc), which makes contact with the substratum, and a proximal contractile cylinder (the stem), which acts as a tether. In this study, the different forces brought into play during tube foot functioning were investigated in two related species. The tube feet of Asterias rubens and Marthasterias glacialis attach to glass with a similar mean tenacity (0.24 and 0.43 MPa, respectively), corresponding to an estimated maximal attachment force of 0.15 and 0.35 N. The contraction force of their retractor muscle averages 0.017 N. The variation of the retractor muscle contraction with its extension ratio follows a typical bell-shaped length–tension curve in which a maximal contraction of approximately 0.04 N is obtained for an extension ratio of approximately 2.3 in both sea star species. The tensile strength of the tube foot stem was investigated considering the two tissues that could assume a load-bearing function, i.e. the retractor muscle and the connective tissue. The latter is a mutable collagenous tissue presenting a fivefold difference in tensile strength between its soft and stiff state. In our experiments, stiffening was induced by disrupting cell membranes or by modifying the ionic composition of the bathing solution. Finally, the force needed to break the tube foot retractor muscle was found to account for 18–25% of the tube foot total breaking force, showing that, although the connective tissue is the tissue layer that supports most of the load exerted on the stem, the contribution of the retractor muscle cannot be neglected in sea stars. All these forces appear well-balanced for proper functioning of the tube feet during the activities of the sea star. They are discussed in the context of two essential activities: the opening of bivalve shells and the maintenance of position in exposed habitats.