Mechanistic insights into phosphatase triggered self-assembly including enhancement of biocatalytic conversion rate
Thornton, Kate and Abul-Haija, Yousef M. and Hodson, Nigel and Ulijn, Rein V. (2013) Mechanistic insights into phosphatase triggered self-assembly including enhancement of biocatalytic conversion rate. Soft Matter, 9 (39). pp. 9430-9439. ISSN 1744-6848 (https://doi.org/10.1039/C3SM51177D)
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Abstract
We report on the mechanistic investigation of alkaline phosphatase (AP) triggered self-assembly and hydrogelation of Fmoc-tyrosine (Fmoc-Y). We studied separately the biocatalytic conversion using HPLC, changes in supramolecular interactions and chirality using CD and fluorescence spectroscopy, nanostructure formation by AFM and gelation by oscillatory rheometry. Three consecutive stages could be distinguished (which may overlap, depending on the enzyme concentration). Typically, the phosphorylated Fmoc-Y (Fmoc-pY) undergoes rapid and complete dephosphorylation, followed by formation of aggregates which reorganise into nanofibres and consequently give rise to gelation. We observed a remarkable enhancement of catalytic activity during the early stages of the self-assembly process, providing evidence for enhancement of enzymatic activation by the supramolecular structures formed. Overall, this study provides a further step in understanding biocatalytic self-assembly.
ORCID iDs
Thornton, Kate, Abul-Haija, Yousef M. ORCID: https://orcid.org/0000-0002-0357-0653, Hodson, Nigel and Ulijn, Rein V. ORCID: https://orcid.org/0000-0001-7974-3779;-
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Item type: Article ID code: 45440 Dates: DateEvent2013Published15 August 2013Published OnlineSubjects: Science > Chemistry
Science > Physics > Solid state physics. NanoscienceDepartment: Faculty of Science > Pure and Applied Chemistry
Technology and Innovation Centre > BionanotechnologyDepositing user: Pure Administrator Date deposited: 28 Oct 2013 18:01 Last modified: 11 Nov 2024 10:31 Related URLs: URI: https://strathprints.strath.ac.uk/id/eprint/45440