Developing new techniques to build biomaterials

Developing new techniques to build biomaterials
A schematic of a protein hydrogel showing regions of folded protein (in red) connected by regions of unfolded protein (in white). Credit: Lorna Dougan/Phospho Animations

Scientists at the University of Leeds have developed an approach that could help in the design of a new generation of synthetic biomaterials made from proteins.

The biomaterials could eventually have applications in joint repair or wound healing as well as other fields of healthcare and food production.

But one of the fundamental challenges is to control and fine tune the way protein blocks assemble into complex protein networks that form the basis of biomaterials.

Scientists at Leeds are investigating how changes to the structure and mechanics of individual protein building blocks—changes at the nanoscale—can alter the structure and mechanics of the at a macro level while preserving the biological function of the protein network.

In a paper published by the scientific journal ACS Nano, the researchers report that they were able to alter the structure of a protein network by removing a specific chemical bond in the protein building blocks. They called these bonds the "protein staples".

With the protein staples removed, the individual protein molecules unfolded more easily when they connect together and assemble into a network. This resulted in a network with regions of folded protein connected by regions containing the resulting in very different mechanical properties for the biomaterial.

A schematic GIFF showing on the left a protein network where protein staples were removed - and on the right, with the protein staples in place. Credit: Lorna Dougan/Phospho Animations

Professor Lorna Dougan, from the School of Physics and Astronomy at Leeds, who supervised the research, said: "Proteins display amazing functional properties. We want to understand how we can exploit this diverse biological functionality in materials which use proteins as building blocks.

"But to do that we need to understand how changes at a nano scale, at the level of individual molecules, alters the structure and behavior of the protein at a macro level."

Dr. Matt Hughes, also from the School of Physics and Astronomy and lead author of the paper, said: "Controlling the protein building block's ability to unfold by removing the "protein staples" resulted in significantly different network architectures with markedly different mechanical behavior and this demonstrates that unfolding of the protein building block plays a defining role in the architecture of protein networks and the subsequent mechanics."

The researchers used facilities at the Astbury Centre for Structural Molecular Biology and School of Physics and Astronomy at Leeds and the ISIS Neutron Muon Source facility at the STFC Rutherford Appleton Laboratory in Oxfordshire. Using beams of neutrons, it allowed them to identify critical changes to the protein network's structure when the nano-staples where removed.

In conjunction with the , Dr. Ben Hanson, a Research Associate in the School of Physics and Astronomy at Leeds, modeled the structural changes taking place. He found that it was specifically the act of protein unfolding during network formation, that was crucial in defining the architecture of the protein hydrogels.

Professor Dougan added: "The ability to change the nanoscale properties of , from a rigid, folded state to a flexible, unfolded state, provides a powerful route to creating functional biomaterials with controllable architecture and mechanics."

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More information: Matt D. G. Hughes et al, Control of Nanoscale In Situ Protein Unfolding Defines Network Architecture and Mechanics of Protein Hydrogels, ACS Nano (2021). DOI: 10.1021/acsnano.1c00353
Journal information: ACS Nano

Citation: Developing new techniques to build biomaterials (2021, July 6) retrieved 28 July 2021 from
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