Elizabeth Gosling

Marine Mussels


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Mefp‐1, Mefp‐2, and so on (Figure 2.11). One distinguishing characteristic of all Mefps is the presence of the post‐translational modification of tyrosine to 3,4‐dihydroxyphenyl‐l‐alanine (DOPA) as well as organic ions, notably iron (Fe3+). Although DOPA is found throughout the byssus, it is present in higher amounts in the Mefps found at the plaque–substrate interface and is believed to be an important component in wet adhesion (Anderson et al. 2010). The plaque has a solid foam structure and is commonly only ~0.15 mm in diameter where it meets the thread and ~2–3 mm at the substrate interface. The six foot proteins are utilised in plaque formation: fp‐3 and fp‐5 are adhesive and adhere to the substrate; fp‐6 is cohesive and binds the former two proteins together; fp‐2 is also cohesive and binds most of the plaque matrix; fp‐4 is cohesive and connects the plaque to the thread; and fp‐1 is cohesive and forms the plaque and thread outer sheath. Fifteen additional foot proteins have been identified through transcriptomic analysis of the foot of the mussel M. californianus (DeMartini et al. 2017). The discovery of these new Mfps sets the groundwork for future biochemical investigations to build a more complete model of byssus structure and function in bioadhesion. Mussels concentrate metals like iron, zinc, copper and manganese more than 100 000‐fold higher in the adhesive plaque compared to their quantities in the sea, which suggests that metal ions play an important role in adhesion (Bandara et al. 2013; Merten 2013). How the mussel processes all these proteins and transition metals into a high‐strength, robust, mechanical adhesive is still not understood (Ornes 2013). For additional information on the fine structure of byssal thread and plaque, see Silverman & Roberto (2011).

Schematic illustration of anatomy of the byssus in Mytilus edulis.

      Source: From Silverman & Roberto (2007). Reproduced with permission from Springer Nature.

Schematic illustration of model of the hierarchical arrangement of a mussel byssal thread.

      Source: From Hagenau et al. (2009). Reproduced with permission from John Wiley & Sons.

Schematic illustration of localisation of adhesive proteins in the byssal thread and plaque of Mytilus.

      Source: From Silverman & Roberto (2011). Reproduced with permission from Springer Nature.

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      Adhesion is a surface physico‐chemical process. It is achieved through a combination of adsorption, mechanical interlocking and molecular diffusion across an interface. The primer proteins fp‐3 and fp‐5, which connect the plaque to the surface, have unusually high DOPA contents (>20%). Both primers are highly hydroxylated and therefore have the potential to form numerous hydrogen bonds (Wiegemann 2005). The primers are also very low‐molecular‐weight proteins, which likely causes them to have greater mobility to dissolve into the interstitial areas of a surface and bond by mechanical interlocking. DOPA not only mediates adhesion to the surface but is also able to form strong hydrogen bonds with hydrophilic polymers, as well as strong complexes with metal ions, metal oxide and silicon oxide present in mineral surfaces (Wiegemann 2005). Also, histidine‐rich domains in preCOLs form crosslinks with metal ions such as Zn2+ and Cu2+ (Harrington & Waite 2007; Figure 2.10B). These bonds are pH sensitive, which in the face of ocean acidification in a climate change scenario could have implications for mussel attachment in suspension culture and for intertidal communities anchored by mussels (O’Donnell et al. 2013; Carrington et al. 2015; see also Chapter 3). Hydrogen bonds and complex formation contribute to the cohesive strength of the adhesive plaque. George et al. (2018) examined the effect of seawater temperature, salinity and dissolved oxygen concentration in M. trossulus, using tensile testing, atomic force miscroscopy (AFM) and amino acid compositional analysis. High temperature (30°C) and hyposalinity (1 psu) had no effect on adhesion strength, while incubation in hypoxia (0.9 mg l−1) caused plaques to have a mottled colouration and to prematurely peel from substrates, leading to a 51% decrease in adhesion strength. AFM imaging of the plaque cuticle found that plaques cured in hypoxia had regions of lower stiffness throughout, indicative of reductions in DOPA crosslinking between adhesive proteins. A better understanding of the dynamics of plaque curing could aid in the design of better synthetic adhesives, particularly in medicine, where adhesion must take place within wet body cavities (see later).

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