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Ligand-observed in-tube NMR in natural products research: A review on enzymatic biotransformations, protein-ligand interactions, and in-cell NMR spectroscopy

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ARABIAN JOURNAL OF CHEMISTRY
卷 16, 期 3, 页码 -

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ELSEVIER
DOI: 10.1016/j.arabjc.2022.104536

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Biotransformations; STD NMR; TR-NOESY NMR; INPHARMA; ILOE NMR; In-cell NMR

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Natural product-observed NMR methods provide significant advantages for in-tube NMR monitoring of enzyme biotransformations and investigating protein-natural product interactions in living cells. The use of a NMR bioreactor allows for investigating natural products as enzyme substrates, monitoring multiple biotransformation products, and studying interactions with protein targets. This method, along with computational techniques, shows promise in protein-natural product recognition research. A rating of: 6/10.
Natural product-observed NMR methods have considerably expanded the potentialities for in-tube NMR monitoring of complex enzymatic biotransformations and investigation of protein -natural product interactions even in living cells. We review, herein, the significant advantages of ligand-observed in-situ NMR monitoring of enzymatic biotransformations without restoring to laborious and time-consuming chromatographic methods. Emphasis will be given to the potential-ities of the use of the NMR bioreactor: (i) to investigate through saturation transfer difference (STD), the capacity of natural products to serve as enzyme substrates, (ii) to monitor multiple bio-transformation products of natural products with the use of immobilized enzymes and (iii) to inves-tigate interactions of biotransformed products with protein targets. The use of STD and its variants, transfer effect Noes for PHArmacophore Mapping (INPHARMA) NMR, in conjunction with com-putational methods, can provide excellent tools in investigating competitive binding modes even in proteins with multiple binding sites. The method has been successfully applied in the study of unsat-urated free fatty acids (UFFAs)-serum albumin complexes in which the location and conformational states of UFFAs could not be determined accurately, despite numerous X-ray structural studies, due to conformational averaging. This combined method, thus, may find promising applications in the field of protein-natural product recognition research. The emerging concept of in-cell NMR and recent applications will be discussed since they can provide atomic level insights into natural product-protein interactions in living cells without the need of isotope labelled techniques.(c) 2023 The Author(s). Published by Elsevier B.V. on behalf of King Saud University. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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