Abstract

The byssal threads of the fan shell Atrina pectinata are non-living functional materials intimately associated with living tissue, which provide an intriguing paradigm of bionic interface for robust load-bearing device. An interfacial load-bearing protein (A. pectinata foot protein-1, apfp-1) with L-3,4-dihydroxyphenylalanine (DOPA)-containing and mannose-binding domains has been characterized from Atrina's foot. apfp-1 was localized at the interface between stiff byssus and the soft tissue by immunochemical staining and confocal Raman imaging, implying that apfp-1 is an interfacial linker between the byssus and soft tissue, that is, the DOPA-containing domain interacts with itself and other byssal proteins via Fe3+–DOPA complexes, and the mannose-binding domain interacts with the soft tissue and cell membranes. Both DOPA- and sugar-mediated bindings are reversible and robust under wet conditions. This work shows the combination of DOPA and sugar chemistry at asymmetric interfaces is unprecedented and highly relevant to bionic interface design for tissue engineering and bionic devices.

Highlights

  • The byssal threads of the fan shell Atrina pectinata are non-living functional materials intimately associated with living tissue, which provide an intriguing paradigm of bionic interface for robust load-bearing device

  • Our results show that the combination of this DOPA-containing and sugar-binding domain plays a significant role in achieving robust load-bearing device and this unprecedented finding has high relevance to bionic interface design for tissue engineering and bionic devices

  • Combining the results of linker protein characterization, confocal imaging and surface forces apparatus (SFA)-based nano-mechanics, we have described an intriguing interaction between tissue and non-tissue components in Atrina in the absence of gradients

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Summary

Introduction

The byssal threads of the fan shell Atrina pectinata are non-living functional materials intimately associated with living tissue, which provide an intriguing paradigm of bionic interface for robust load-bearing device. There appear to be two strategies in biology for mitigating contact damage between mismatched loadbearing materials: (A) using a strong interfacial adhesion over an increased surface area of contact (thereby reducing the load per unit area), or (B) creating an interface that relies on molecular gradients. The former, suitable for bulky materials, is the strategy employed in the tendon–muscle junction[4,5]. Our results show that the combination of this DOPA-containing and sugar-binding domain plays a significant role in achieving robust load-bearing device and this unprecedented finding has high relevance to bionic interface design for tissue engineering and bionic devices

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