Exploiting mammalian low-complexity domains for liquid-liquid phase separation-driven underwater adhesive coatings

被引:75
作者
Cui, Mengkui [1 ,2 ,3 ]
Wang, Xinyu [1 ,2 ,4 ]
An, Bolin [1 ]
Zhang, Chen [1 ]
Gui, Xinrui [2 ,5 ]
Li, Ke [1 ]
Li, Yingfeng [1 ,2 ,4 ]
Ge, Peng [6 ]
Zhang, Junhu [6 ]
Liu, Cong [5 ]
Zhong, Chao [1 ]
机构
[1] ShanghaiTech Univ, Sch Phys Sci & Technol, Mat & Phys Biol Div, Shanghai 201210, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Organ Chem, Shanghai 200032, Peoples R China
[4] Chinese Acad Sci, Shanghai Inst Ceram, Shanghai 200050, Peoples R China
[5] Chinese Acad Sci, Interdisciplinary Res Ctr Biol & Chem, Shanghai Inst Organ Chem, Shanghai 200032, Peoples R China
[6] Jilin Univ, Coll Chem, State Key Lab Supramol Struct & Mat, Changchun 130012, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
CELL-FREE FORMATION; GRANULES; COACERVATION; AMYLOIDS; DROPLETS;
D O I
10.1126/sciadv.aax3155
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Many biological materials form via liquid-liquid phase separation (LLPS), followed by maturation into a solid-like state. Here, using a biologically inspired assembly mechanism designed to recapitulate these sequential assemblies, we develop ultrastrong underwater adhesives made from engineered proteins containing mammalian low-complexity (LC) domains. We show that LC domain-mediated LLPS and maturation substantially promotes the wetting, adsorption, priming, and formation of dense, uniform amyloid nanofiber coatings on diverse surfaces (e.g., Teflon), and even penetrating difficult-to-access locations such as the interiors of microfluidic devices. Notably, these coatings can be deposited on substrates over a broad range of pH values (3 to 11) and salt concentrations (up to 1 M NaCl) and exhibit strong underwater adhesion performance. Beyond demonstrating the utility of mammalian LC domains for driving LLPS in soft materials applications, our study illustrates a powerful example of how combining LLPS with subsequent maturation steps can be harnessed for engineering protein-based materials.
引用
收藏
页数:12
相关论文
共 41 条
[1]
Diverse Supramolecular Nanofiber Networks Assembled by Functional Low-Complexity Domains [J].
An, Bolin ;
Wang, Xinyu ;
Cui, Mengkui ;
Gui, Xinrui ;
Mao, Xiuhai ;
Liu, Yan ;
Li, Ke ;
Chu, Cenfeng ;
Pu, Jiahua ;
Ren, Susu ;
Wang, Yanyi ;
Zhong, Guisheng ;
Lu, Timothy K. ;
Liu, Cong ;
Zhong, Chao .
ACS NANO, 2017, 11 (07) :6985-6995
[2]
Adaptation to stressors by Systemic Protein Amyloidogenesis [J].
Audas, Timothy E. ;
Audas, Danielle E. ;
Jacob, Mathieu D. ;
Ho, J. J. David ;
Khacho, Mireille ;
Wang, Miling ;
Perera, J. Kishan ;
Gardiner, Caroline ;
Bennett, Clay A. ;
Head, Trajen ;
Kryvenko, Oleksandr N. ;
Jorda, Merce ;
Daunert, Sylvia ;
Malhotra, Arun ;
Trinkle-Mulcahy, Laura ;
Gonzalgo, Mark L. ;
Lee, Stephen .
DEVELOPMENTAL CELL, 2016, 39 (02) :155-168
[3]
Biomolecular condensates: organizers of cellular biochemistry [J].
Banani, Salman F. ;
Lee, Hyun O. ;
Hyman, Anthony A. ;
Rosen, Michael K. .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2017, 18 (05) :285-298
[4]
Mechanisms and Consequences of Macromolecular Phase Separation [J].
Bergeron-Sandoval, Louis-Philippe ;
Safaee, Nozhat ;
Michnick, Stephen W. .
CELL, 2016, 165 (05) :1067-1079
[5]
Physical principles of intracellular organization via active and passive phase transitions [J].
Berry, Joel ;
Brangwynne, Clifford P. ;
Haataja, Mikko .
REPORTS ON PROGRESS IN PHYSICS, 2018, 80 (04)
[6]
Amyloid-like Self-Assembly of a Cellular Compartment [J].
Boke, Elvan ;
Ruer, Martine ;
Wuehr, Martin ;
Coughlin, Margaret ;
Lemaitre, Regis ;
Gygi, Steven P. ;
Alberti, Simon ;
Drechsel, David ;
Hyman, Anthony A. ;
Mitchison, Timothy J. .
CELL, 2016, 166 (03) :637-650
[7]
Brangwynne CP, 2015, NAT PHYS, V11, P899, DOI [10.1038/nphys3532, 10.1038/NPHYS3532]
[8]
Germline P Granules Are Liquid Droplets That Localize by Controlled Dissolution/Condensation [J].
Brangwynne, Clifford P. ;
Eckmann, Christian R. ;
Courson, David S. ;
Rybarska, Agata ;
Hoege, Carsten ;
Gharakhani, Joebin ;
Juelicher, Frank ;
Hyman, Anthony A. .
SCIENCE, 2009, 324 (5935) :1729-1732
[9]
ALS Mutations Disrupt Phase Separation Mediated by α-Helical Structure in the TDP-43 Low-Complexity C-Terminal Domain [J].
Conicella, Alexander E. ;
Zerze, Gul H. ;
Mittal, Jeetain ;
Fawzi, Nicolas L. .
STRUCTURE, 2016, 24 (09) :1537-1549
[10]
Modular genetic design of multi-domain functional amyloids: insights into self-assembly and functional properties [J].
Cui, Mengkui ;
Qi, Qi ;
Gurry, Thomas ;
Zhao, Tianxin ;
An, Bolin ;
Pu, Jiahua ;
Gui, Xinrui ;
Cheng, Allen A. ;
Zhang, Siyu ;
Xun, Dongmin ;
Becce, Michele ;
Briatico-Vangosa, Francesco ;
Liu, Cong ;
Lu, Timothy K. ;
Zhong, Chao .
CHEMICAL SCIENCE, 2019, 10 (14) :4004-4014