Synthesis of 13C/19F/2H labeled indoles for use as tryptophan precursors for protein NMR spectroscopy
Author:
Affiliation:
1. Latvian Institute of Organic Synthesis
2. Riga
3. Latvia
4. ARC Centre of Excellence for Innovations in Peptide & Protein Science
5. Research School of Chemistry
6. Australian National University
7. Canberra
8. Australia
Abstract
Cell-free protein synthesis using 19F–13C and 1H–13C spin pair containing indoles as tryptophan precursors enables site-specific labeling of proteins for 19F NMR and TROSY NMR studies.
Funder
Australian Research Council
European Regional Development Fund
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2021/OB/D1OB00611H
Reference74 articles.
1. NMR Studies of Structure and Function of Biological Macromolecules (Nobel Lecture)
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1. Genetic Encoding of Fluoro-l-tryptophans for Site-Specific Detection of Conformational Heterogeneity in Proteins by NMR Spectroscopy;Journal of the American Chemical Society;2024-04-30
2. Decorating phenylalanine side-chains with triple labeled 13C/19F/2H isotope patterns;Journal of Biomolecular NMR;2024-03-21
3. Enlarging the scenario of site directed 19F labeling for NMR spectroscopy of biomolecules;Scientific Reports;2023-12-12
4. Decorating phenylalanine side-chains with triple labeled 13 C/ 19 F/ 2 H isotope patterns;2023-10-17
5. In-Cell Structural Biology by NMR: The Benefits of the Atomic Scale;Chemical Reviews;2022-03-31
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