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Research Article

A supramolecular method to control protein assembly using a biogenic polyamine

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Received 13 May 2024, Accepted 24 Jul 2024, Published online: 27 Jul 2024

References

  • Saad S, Cereghetti G, Feng Y, et al. Reversible protein aggregation is a protective mechanism to ensure cell cycle restart after stress. Nat Cell Biol. 2017;19(10):1202–1213. doi: 10.1038/ncb3600
  • Michaels TCT, Weber CA, Mahadevan L. Optimal control strategies for inhibition of protein aggregation. Proc Natl Acad Sci USA. 2019;116(29):14593–14598. doi: 10.1073/pnas.1904090116
  • Fassler JS, Skuodas S, Weeks DLP, et al. Protein aggregation and disaggregation in cells and development. J Mol Biol. 2021;433(21):167215. doi: 10.1016/j.jmb.2021.167215
  • Wolozin B. Mol. Neurodegener. 2012;7(1):56. doi: 10.1186/1750-1326-7-56
  • Nooren IMAT, M J. Structural characterization and functional significance of transient protein-protein interactions. J Mol Biol. 2003;325(5):991–1018. doi: 10.1016/S0022-2836(02)01281-0
  • Rajan R, Ahmed S, Sharma N, et al. Review of the current state of protein aggregation inhibition from a materials chemistry perspective: special focus on polymeric materials. Mater Adv. 2021;2(4):1139–1176. doi: 10.1039/D0MA00760A
  • Mabonga LK, P A. Biophys. Rev. 2019;11(4):559–581. doi: 10.1007/s12551-019-00570-x
  • Ghosh P, De P. ACS App. Bio Mater. 2020;3(10):6598–6625. doi: 10.1021/acsabm.0c01021
  • Oliveri V, Vecchio G. Cyclodextrins as protective agents of protein aggregation: an overview. Chem Asian J. 2016;11(11):1648–1657. doi: 10.1002/asia.201600259
  • Consoli GML, Tosto R, Baglieri A, et al., Novel Peptide-Calix[4]arene conjugate inhibits Aβ aggregation and rescues neurons from Aβ’s oligomers cytotoxicity in vitro. ACS Chem Neurosci. 2021;12(8):1449–1462. doi: 10.1021/acschemneuro.1c00117
  • Xu Z, Jia S, Wang W, et al. Heteromultivalent peptide recognition by co-assembly of cyclodextrin and calixarene amphiphiles enables inhibition of amyloid fibrillation. Nat Chem. 2019;11(1):86–93. doi: 10.1038/s41557-018-0164-y
  • Maity D. Biophys. Chem. 2023;297:107022. doi: 10.1016/j.bpc.2023.107022
  • Shetty D, Khedkar JK, Park KM, et al. Can we beat the biotin-avidin pair?: cucurbit[7]uril-based ultrahigh affinity host-guest complexes and their applications. Chem Soc Rev. 2015;44(23):8747–8761. doi: 10.1039/C5CS00631G
  • Liu W, Samanta SK, Smith BD, et al. Synthetic mimics of biotin/(strept)avidin. Chem Soc Rev. 2017;46(9):2391–2403. doi: 10.1039/C7CS00011A
  • Heitmann LM, Taylor AB, Hart PJU, et al. Sequence-specific recognition and cooperative dimerization of N-Terminal aromatic peptides in aqueous solution by a synthetic Host. J Am Chem Soc. 2006;128(38):12574–12581. doi: 10.1021/ja064323s
  • de Vink PJ, Briels JM, Schrader T, et al. A binary bivalent supramolecular assembly platform based on Cucurbit[8]uril and dimeric adapter protein 14-3-3. Angew Chem Int Ed. 2017;56(31):8998–9002. doi: 10.1002/anie.201701807
  • Engilberge S, Rennie ML, Dumont EC, et al. Tuning protein frameworks via auxiliary supramolecular interactions. ACS Nano. 2019;13(9):10343–10350. doi: 10.1021/acsnano.9b04115
  • Guagnini F, Engilberge S, Ramberg KO, et al. Engineered assembly of a protein–cucurbituril biohybrid. Chem Commun. 2020;56(3):360–363. doi: 10.1039/C9CC07198A
  • Ramberg KO, Guagnini F, Engilberge S, et al. Segregated protein-Cucurbit[7]uril crystalline architectures via Modulatory Peptide Tectons. Chem Eur J. 2021;27(59):14619–14627. doi: 10.1002/chem.202103025
  • Liu S, Ruspic C, Mukhopadhyay P, et al. The Cucurbit[n]uril family: prime components for self-sorting systems. J Am Chem Soc. 2005;127(45):15959–15967. doi: 10.1021/ja055013x
  • Assaf KIN, Nau W. Cucurbiturils: from synthesis to high-affinity binding and catalysis. Chem Soc Rev. 2015;44(2):394–418. doi: 10.1039/C4CS00273C
  • Kim KL, Sung G, Sim J, et al. Supramolecular latching system based on ultrastable synthetic binding pairs are versatile tools for protein imaging. Nat Commun. 2018;9(1):1712. doi: 10.1038/s41467-018-04161-4
  • Barooah N, Kunwar A, Khurana R, et al. Stimuli-responsive Cucurbit[7]uril-mediated BSA nanoassembly for uptake and release of doxorubicin. Chem Asian J. 2017;12(1):122–129. doi: 10.1002/asia.201601411
  • Pegg AE. Functions of Polyamines in mammals. J Biol Chem. 2016;291(29):14904–14912. doi: 10.1074/jbc.R116.731661
  • Chen Y, Huang Z, Zhao H, et al. Supramolecular chemotherapy: cooperative enhancement of antitumor activity by combining controlled release of oxaliplatin and consumption of spermine by Cucurbit[7]uril. ACS Appl Mater Inter. 2017;9(10):8602–8608. doi: 10.1021/acsami.7b01157
  • Zhang H, Liu M, Zhu X, et al. Detection of spermine using Cucurbit[7]uril-phenazopyridine host-guest inclusion complex as a platform. Chem Lett. 2020;50(1):154–157. doi: 10.1246/cl.200667
  • Wang S-R, Wang J-Q, Xu G-H, et al. The Cucurbit[7]Uril-based supramolecular chemistry for reversible B/Z-DNA transition. Ad Sci. 2018;5(7):1800231. doi: 10.1002/advs.201800231
  • Halterman RL, Moore JL, Mannel LM. Disrupting aggregation of tethered rhodamine B dyads through inclusion in Cucurbit[7]uril. J Org Chem. 2008;73(8):3266–3269. doi: 10.1021/jo7026432
  • Lee J, Jang S, Kim M, et al. Trapping alkali halide cluster ions inside the Cucurbit[7]uril cavity. J Phys Chem Lett. 2022;13(41):9581–9588. doi: 10.1021/acs.jpclett.2c02583
  • Chinai JM, Taylor AB, Ryno LM, et al. Molecular recognition of insulin by a synthetic receptor. J Am Chem Soc. 2011;133(23):8810–8813. doi: 10.1021/ja201581x
  • Hu C, Grimm L, Prabodh A, et al. Covalent cucurbit[7]uril-dye conjugates for sensing in aqueous saline media and biofluids. Chem Sci. 2020;11(41):11142–11153. doi: 10.1039/D0SC03079A

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