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Spider silk proteins form hydrogels at body temperature

The previously unobserved phenomenon could lead to tissue engineering and drug delivery applications

by Payal Dhar, special to C&EN
September 7, 2022


The hydrogels stained with a fluorescent dye that binds to amyloid structures.
Credit: Tina Arndt

Hydrogels made from spider silk proteins are stained with a green fluorescent dye that binds to amyloid structures.

Spider silk proteins known as spidroins can form hydrogels at body temperature, according to a new study. The study’s authors think that the gels could be tailored for a variety of biomedical applications, such as tissue engineering and drug delivery (Nat. Commun. 2022, DOI: 10.1038/s41467-022-32093-7).

Hydrogels are 3D polymer networks that can hold large amounts of water. Spider silk is biocompatible and doesn’t tend to trigger immune reactions in people, making the materials safe for biomedical purposes, says study first author Tina Arndt, a researcher at Karolinska Institute.

Arndt and her colleagues discovered that spidroins could form hydrogels by chance. The scientists had sent a sample of spidroins made by bacteria to collaborators, but the package was delayed in transit. When it finally arrived, the protein sample had gelled unexpectedly. On analyzing the different parts of the protein, they found that its gel-forming ability was due to the spidroin’s N-terminal (NT) domain, the amino acids at the start of the protein chain.

Spidroins are normally stored as a soluble liquid in the spider’s silk gland. When the spider starts to spin its web, the proteins undergo structural changes that cause them to solidify. Specifically, the proteins’ C-terminal (CT) domain, which is at the other end of the protein chain from the NT, unfolds, converting from a helical form to an amyloid-like one.

Researchers had previously assumed the NT domain always remained stable and soluble. Arndt and colleagues, however, found that at high enough concentrations and at normal body temperature, the NT does undergo structural changes while forming a hydrogel.

In lab experiments, the researchers created fusion proteins by combining the NT domains with other proteins, including an enzyme. They found the fusion proteins retained their biological functions.

R. Helen Zha, who studies bioinspired and biomimetic materials at the Rensselaer Polytechnic Institute, calls the discovery of this new spider silk ability fascinating. The hydrogels reported in this study are incredibly versatile in that they can easily incorporate a variety of bioactive proteins, she says.

Arndt and colleagues are working to develop an injectable protein solution that turns into a hydrogel inside the body for drug delivery and tissue regeneration applications.



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