Ingo Grunwald

Siloxane fouling release coatings are currently the only viable non-toxic commercial alternative to toxic biocide antifouling paints. However, they only partially inhibit biofouling since biofilms remain a major issue. With the aim to improve the bacterial resistance of siloxane coatings modified with non-ionic surfactant (NIS), antioxidant (AO) or both NIS/AO, the ability of PEG-silane co-cross-linker was investigated to reduce Cobetia marina adhesion and multispecies biofilm formation from natural seawater. Surface physical-chemical and physical-mechanical parameters relevant to bio-adhesion were estimated before the testing of the biofilm formation. Slightly reduced biofilm from C. marina and sharply reduced multispecies biofilm, formed in natural sea water, were found on the PEG-silane co-cross-linked coatings without modifying additives. However, both C. marina growth and biofilm formation from natural sea water were sharply reduced on the PEG-silane co-cross-linked coatings containing NIS or AO, even more, no C. marina adhesion was seen on the coating containing NIS and AO simultaneously. Possible explanations of the observed effects are presented in this article. It was concluded that the PEG-silane co-cross-linker, toghether with NIS and AO, can be used as an efficient tool to additionally reduce the bioadhesion of Gram-negative marine bacteria and multispecies biofilm formation on siloxane antifouling coatings.

Salamanders have developed a wide variety of antipredator mechanisms, including tail autotomy, colour patterns, and noxious skin secretions. As an addition to these tactics, the red-legged salamander (Plethodon shermani) uses adhesive secretions as part of its defensive strategy. The high bonding strength, the fast-curing nature, and the composition of the biobased materials makes salamander adhesives interesting for practical applications in the medical sector. To understand the adhesive secretions ofP.shermani, its components were chemically analysed by energy dispersive X-ray spectroscopy (EDX), inductively coupled plasma mass spectrometry (ICP-MS), amino acid analysis, and spectroscopy (ATR-IR, Raman). In addition, proteins were separated by gel-electrophoresis and selected spots were characterised by peptide mass fingerprinting. The salamander secretion contains a high amount of water and predominantly proteins (around 77% in the dry stage). The gel-electrophoresis and peptide mass fingerprint analyses revealed ade novoset of peptides/proteins, largely with a pI between 5.0 and 8.0 and a molecular mass distribution between 10 and 170 kDa. Only low homologies with other proteins present in known databases could be identified. The results indicate that the secretions of the salamanderPlethodonclearly differ chemically from those shown for other glue-producing terrestrial or marine species and thus represent a unique glue system.

The goose barnacle Dosima fascicularis produces an excessive amount of adhesive (cement), which has a double function, being used for attachment to various substrata and also as a float (buoy). This paper focuses on the chemical composition of the cement, which has a water content of 92%. Scanning electron microscopy with EDX was used to measure the organic elements C, O and N in the foam-like cement. Vibrational spectroscopy (FTIR, Raman) provided further information about the overall secondary structure, which tended towards a β-sheet. Disulphide bonds could not be detected by Raman spectroscopy. The cystine, methionine, histidine and tryptophan contents were each below 1% in the cement. Analyses of the cement revealed a protein content of 84% and a total carbohydrate content of 1.5% in the dry cement. The amino acid composition, 1D/2D-PAGE and MS/MS sequence analysis revealed a de novo set of peptides/proteins with low homologies with other proteins such as the barnacle cement proteins, largely with an acidic pI between 3.5 and 6.0. The biochemical composition of the cement of D. fascicularis is similar to that of other barnacles, but it shows interesting variations.

In this work, we combine nature’s amazing bioadhesive catechol with the excellent bioinert synthetic macromolecule hyperbranched polyglycerol (hPG) to prepare antifouling surfaces. hPG can be functionalized by different amounts of catechol groups for multivalent anchoring and cross-linking because of its highly branched architecture. The catecholic hPGs can be immobilized on various surfaces including metal oxides, noble metals, ceramics, and polymers via simple incubation procedures. The effect of the catechol amount on the immobilization, surface morphology, stability, and antifouling performance of the coatings was studied. Both anchoring and cross-linking interactions provided by catechols can enhance the stability of the coatings. When the catechol groups on the hPG are underrepresented, the tethering of the coating is not effective; while an overrepresentation of catechol groups leads to protein adsorption and cell adhesion. Thus, only a well-balanced amount of catechols as optimized and described in this work can supply the coatings with both good stability and antifouling ability.

Material-independent and bioinert hierarchical polymer multilayer coatings are presented. Chemically active catecholic hyperbranched polyglycerols (hPGs) form a foundation layer on a versatile surface via multivalent anchoring and crosslinking, the activity of which is shielded by the bioinert catecholic hPGs. Mono-catecholic hPGs finally terminate all of the free catechols to build a flexible bioinert top layer. These coatings perfectly prevent protein and cell adhesion.

We introduce a novel technique for an initial identification of peptide sequences that specifically bind to material surfaces based on the matrix assisted laser desorption ionization time of flight mass spectrometry (MALDI-ToF MS) depletion method. The technique relies upon time-resolved, sensitive measurements of the MALDI-ToF MS peak signals acquired from a solution containing several peptides placed in contact with an inorganic surface, in our case amorphous SiO₂. Large errors intrinsic in the MALDI-ToF MS spectral analysis and uncertainties arising from the adsorption behaviour of peptide mixtures limit the predictive power of the method. However, when combined with other characterisation and modelling techniques, such as High-Performance Liquid Chromatography (HPLC), Atomic Force Microscopy (AFM), Quartz Crystal Microbalance with Dissipation (QCM-D) and Molecular Dynamics (MD), it can be used as a guide to identify novel material-binding peptide sequences, such as TPGSR for SiO₂. The strategy presented in this work may have an impact on the design and synthesis of novel hybrid biomaterials based on the biomolecular recognition of inorganic surfaces.

The influence of adhesion on molecular conformations—besides solely molecule orientation—and vice versa was rarely considered in adhesion science due to the difficult analysis of conformational equilibria, in general, and the high number of possible conformations in classical polymers, in particular. Fortunately, some insight is available from the interphase chemistry of proteins due to the importance regarding their biological function in heterogeneous systems. Peptides and proteins are, thus, ideal model systems for the experimental and theoretical investigation of conformational changes in interphases. The conformational equilibrium of any kind of compound or, more specifically, a polymer interacting with a surface must differ in the interphase when compared with the bulk. This is also the case for common adhesives. Therefore, we define that the interphase of an adhesive bond is the area in which the chemical composition or the conformational equilibrium differs from that of the bulk phase.