Microbially Synthesized Repeats of Mussel Foot Protein Display Enhanced Underwater Adhesion

2018 ◽  
Vol 10 (49) ◽  
pp. 43003-43012 ◽  
Author(s):  
Eugene Kim ◽  
Bin Dai ◽  
James B. Qiao ◽  
Wenlu Li ◽  
John D. Fortner ◽  
...  
Author(s):  
Eugene Kim ◽  
Juya Jeon ◽  
Yaguang Zhu ◽  
Ethan D. Hoppe ◽  
Young-Shin Jun ◽  
...  

Soft Matter ◽  
2017 ◽  
Vol 13 (48) ◽  
pp. 9122-9131 ◽  
Author(s):  
Ilia Kaminker ◽  
Wei Wei ◽  
Alex M. Schrader ◽  
Yeshayahu Talmon ◽  
Megan T. Valentine ◽  
...  

Single-component peptide coacervates mimicking mussel foot protein-3S were adapted for rapid pressure-sensitive wet adhesion. The coacervate upon compression exhibited orders of magnitude higher underwater adhesion at 2 N m−1 than thin films of the most adhesive mussel-foot-derived peptides reported to date.


2019 ◽  
Author(s):  
Amal Narayanan ◽  
Joshua Menefee ◽  
Qianhui Liu ◽  
Ali Dhinojwala ◽  
Abraham Joy

Inspired from the one-component self-coacervation of tropoelastin and mussel foot protein-3s, we created the first non-ionic, single component coacervates that can coacervate in a all ranges of pH (acidic to basic) and wide range of ionic strengths with degradability, rapid curing and strong underwater adhesion. In contrast to the complex coacervates, these ‘charge-free’ coacervates are potential candidates as tissue adhesives and sealants, adhesives for sensor attachment to wet skin, and as sprayable adhesives. Their potential use in the clinic arises from their enhanced stability to changes in external conditions, cytocompatibility, biodegradability and modular nature in incorporating various functional groups and crosslinkers.


2019 ◽  
Author(s):  
Amal Narayanan ◽  
Joshua Menefee ◽  
Qianhui Liu ◽  
Ali Dhinojwala ◽  
Abraham Joy

Inspired from the one-component self-coacervation of tropoelastin and mussel foot protein-3s, we created the first non-ionic, single component coacervates that can coacervate in a all ranges of pH (acidic to basic) and wide range of ionic strengths with degradability, rapid curing and strong underwater adhesion. In contrast to the complex coacervates, these ‘charge-free’ coacervates are potential candidates as tissue adhesives and sealants, adhesives for sensor attachment to wet skin, and as sprayable adhesives. Their potential use in the clinic arises from their enhanced stability to changes in external conditions, cytocompatibility, biodegradability and modular nature in incorporating various functional groups and crosslinkers.


2020 ◽  
Vol 511 ◽  
pp. 145589
Author(s):  
Mengdi Zhao ◽  
Liyi Bai ◽  
Joonkyung Jang

2018 ◽  
Vol 54 (89) ◽  
pp. 12642-12645 ◽  
Author(s):  
Pulakesh Aich ◽  
Jaeyeon An ◽  
Byeongseon Yang ◽  
Young Ho Ko ◽  
Junghyun Kim ◽  
...  

A spider with mussel: a supramolecular fiber formed by a spider dragline protein was tuned to have underwater adhesion property by genetic fusion of a mussel foot protein.


2021 ◽  
Vol 118 (41) ◽  
pp. e2104975118
Author(s):  
Mengyue Sun ◽  
Nityanshu Kumar ◽  
Ali Dhinojwala ◽  
Hunter King

Thermodynamics tells us to expect underwater contact between two hydrophobic surfaces to result in stronger adhesion compared to two hydrophilic surfaces. However, the presence of water changes not only energetics but also the dynamic process of reaching a final state, which couples solid deformation and liquid evacuation. These dynamics can create challenges for achieving strong underwater adhesion/friction, which affects diverse fields including soft robotics, biolocomotion, and tire traction. Closer investigation, requiring sufficiently precise resolution of film evacuation while simultaneously controlling surface wettability, has been lacking. We perform high-resolution in situ frustrated total internal reflection imaging to track underwater contact evolution between soft-elastic hemispheres of varying stiffness and smooth–hard surfaces of varying wettability. Surprisingly, we find the exponential rate of water evacuation from hydrophobic–hydrophobic (adhesive) contact is three orders of magnitude lower than that from hydrophobic–hydrophilic (nonadhesive) contact. The trend of decreasing rate with decreasing wettability of glass sharply changes about a point where thermodynamic adhesion crosses zero, suggesting a transition in mode of evacuation, which is illuminated by three-dimensional spatiotemporal height maps. Adhesive contact is characterized by the early localization of sealed puddles, whereas nonadhesive contact remains smooth, with film-wise evacuation from one central puddle. Measurements with a human thumb and alternatively hydrophobic/hydrophilic glass surface demonstrate practical consequences of the same dynamics: adhesive interactions cause instability in valleys and lead to a state of more trapped water and less intimate solid–solid contact. These findings offer interpretation of patterned texture seen in underwater biolocomotive adaptations as well as insight toward technological implementation.


2021 ◽  
Author(s):  
Xing Su ◽  
Wenyue Xie ◽  
Pudi Wang ◽  
Zhuoling Tian ◽  
Hao Wang ◽  
...  

It is challenging for injectable hydrogels to achieve high underwater adhesiveness. Based on this concern, we report a fully physically crosslinked injectable hydrogel composed of gelatin, tea polyphenols and urea,...


Biomimetics ◽  
2019 ◽  
Vol 4 (2) ◽  
pp. 30 ◽  
Author(s):  
Amanda Andersen ◽  
Yaqing Chen ◽  
Henrik Birkedal

The blue mussel incorporates the polyphenolic amino acid l-3,4-dihydroxyphenylalanine (DOPA) to achieve self-healing, pH-responsiveness, and impressive underwater adhesion in the byssus threads that ensure the survival of the animal. This is achieved by a pH-dependent and versatile reaction chemistry of polyphenols, including both physical interactions as well as reversible and irreversible chemical bonding. With a short introduction to the biological background, we here review the latest advances in the development of smart materials based on the metal-chelating capabilities of polyphenols. We focus on new ways of utilizing the polyphenolic properties, including studies on the modifications of the nearby chemical environment (on and near the polyphenolic moiety) and on the incorporation of polyphenols into untraditional materials.


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