Temperature-regulated Hybrid Protein Hydrogel for Recyclable Extraction of Uranium from Seawater
Source abstract
Abstract
To extend the temperature-controlled biohydrogel system from peptides to proteins, we synthesized a protein hydrogel by integrating super uranyl binding protein (SUP) and N-isopropylacrylamide (NIPAM). The protein hydrogel adsorbs trace uranyl from seawater and releases it only by separate temperature regulation. We explored the mechanism of the hybrid hydrogel to regulate SUP activity by comparing different immobilized sites and analyzing viscoelastic effectiveness. Stretching amino acid residues near the uranyl binding site plays a key role in regulation, and the volume variation of the hybrid hydrogel across the low critical solution temperature provides sufficient driving force to deform the SUP. This work demonstrates the prospective potential of using other proteins in hydrogel systems for functional regulation.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Radioactive element chemistry and processing · Polymer Surface Interaction Studies · Connective tissue disorders research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Collaborative Innovation Center of Chemistry for Life Sciences, Nanjing University, Nanjing 210023, China
State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing 210023, China
Department of Chemistry, The Chinese University of Hong Kong, Hong Kong 999077, China
Funding
National Natural Science Foundation of China · Ministry of Science and Technology of China Key Project
References (35)
Show source-provided references
1. 10.1016/j.jare.2013.07.00610.1016/j.jare.2013.07.006 ↗
2. 10.1007/s40204-018-0095-010.1007/s40204-018-0095-0 ↗
3. 10.1039/c8mh01160e10.1039/c8mh01160e ↗
4. 10.1038/s41578-019-0148-610.1038/s41578-019-0148-6 ↗
5. 10.1021/acsnano.7b0351310.1021/acsnano.7b03513 ↗
6. 10.1039/c5sc02234g10.1039/c5sc02234g ↗
7. 10.1016/j.carbpol.2020.11583910.1016/j.carbpol.2020.115839 ↗
8. 10.1021/acsami.8b0647510.1021/acsami.8b06475 ↗
9. 10.1016/j.jclepro.2020.12470310.1016/j.jclepro.2020.124703 ↗
10. 10.1002/adfm.20170214710.1002/adfm.201702147 ↗
11. 10.1002/advs.20190008510.1002/advs.201900085 ↗
12. 10.1021/acs.chemrev.0c0034510.1021/acs.chemrev.0c00345 ↗
13. 10.1016/j.pmatsci.2020.10070210.1016/j.pmatsci.2020.100702 ↗
14. 10.1021/bm100035f10.1021/bm100035f ↗
15. 10.1021/acsami.9b1930610.1021/acsami.9b19306 ↗
16. 10.1021/acs.accounts.0c0083210.1021/acs.accounts.0c00832 ↗
17. 10.1038/nature1147510.1038/nature11475 ↗
18. 10.1016/j.cej.2021.13058910.1016/j.cej.2021.130589 ↗
19. 10.1021/acs.chemrev.7b0035510.1021/acs.chemrev.7b00355 ↗
20. 10.1016/j.chempr.2021.02.00610.1016/j.chempr.2021.02.006 ↗
21. 10.1038/nchem.185610.1038/nchem.1856 ↗
22. 10.1016/j.chempr.2021.01.00810.1016/j.chempr.2021.01.008 ↗
23. 10.1021/acsami.6b1596810.1021/acsami.6b15968 ↗
24. 10.1002/anie.20190619110.1002/anie.201906191 ↗
25. 10.1002/anie.20200738310.1002/anie.202007383 ↗
26. 10.1039/c7py01206c10.1039/c7py01206c ↗
27. 10.1016/j.msec.2020.11151710.1016/j.msec.2020.111517 ↗
28. 10.1038/nchembio.241610.1038/nchembio.2416 ↗
29. 10.1039/b716526a10.1039/b716526a ↗
30. 10.1021/ja508756310.1021/ja5087563 ↗
31. 10.1007/s00396-011-2383-210.1007/s00396-011-2383-2 ↗
32. 10.1038/1621910.1038/16219 ↗
33. 10.1039/c3cp52142g10.1039/c3cp52142g ↗
34. 10.1038/s41570-017-008310.1038/s41570-017-0083 ↗
35. 10.1016/s0168-3659(97)00151-x10.1016/s0168-3659(97)00151-x ↗