Literature DB >> 25728393

Fluoro amino acids: a rarity in nature, yet a prospect for protein engineering.

Corinna Odar1, Margit Winkler, Birgit Wiltschi.   

Abstract

Fluoro amino acids are highly valuable compounds constantly gaining relevance in diverse fields of the biosciences as well as in the pharmaceutical industry. The value of these compounds can be attributed to the properties of the extremely electronegative fluorine atom. This atom forms a highly polarized bond of extraordinary strength with carbon. The formation of the fluorine-carbon bond is challenging: its chemical synthesis demands harsh reaction conditions and to date only one class of enzyme has been found capable of introducing the fluoride ion into an organic compound. Most of these fluorinating enzymes participate in the biosynthesis of 4-fluoro-L-threonine, the only fluoro amino acid of natural origin discovered so far. Despite their scarcity in nature, fluoro amino acids are valuable tools to fluorinate proteins. The fluoro protein variants often show improved stability and folding as well as altered activity and fluorescence characteristics. This review details the biosynthesis of 4-fluoro-L-threonine with a special focus on the fluorinating enzymes. Moreover, we elaborate on the application of fluoro amino acids as building blocks for fluorinated protein variants. Insight into different techniques to incorporate fluoro amino acids into proteins is also provided. We highlight prospects and the current relevance of fluoro amino acids as a tool to engineer proteins with novel traits.
Copyright © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  Fluorinase; Fluorinated amino acid; Genetic code expansion; Non-canonical amino acid; Synthetic biology

Mesh:

Substances:

Year:  2015        PMID: 25728393     DOI: 10.1002/biot.201400587

Source DB:  PubMed          Journal:  Biotechnol J        ISSN: 1860-6768            Impact factor:   4.677


  13 in total

1.  4-Fluoroprolines: Conformational Analysis and Effects on the Stability and Folding of Peptides and Proteins.

Authors:  Robert W Newberry; Ronald T Raines
Journal:  Top Heterocycl Chem       Date:  2016-01-12

2.  Functional analysis of iodotyrosine deiodinase from drosophila melanogaster.

Authors:  Abhishek Phatarphekar; Steven E Rokita
Journal:  Protein Sci       Date:  2016-09-26       Impact factor: 6.725

3.  Perfluoro-tert-butyl Homoserine Is a Helix-Promoting, Highly Fluorinated, NMR-Sensitive Aliphatic Amino Acid: Detection of the Estrogen Receptor·Coactivator Protein-Protein Interaction by 19F NMR.

Authors:  Caitlin M Tressler; Neal J Zondlo
Journal:  Biochemistry       Date:  2017-02-15       Impact factor: 3.162

4.  Catalytic Asymmetric Mannich Reaction of α-Fluoronitriles with Ketimines: Enantioselective and Diastereodivergent Construction of Vicinal Tetrasubstituted Stereocenters.

Authors:  Ransheng Ding; Zeus A De Los Santos; Christian Wolf
Journal:  ACS Catal       Date:  2019-02-06       Impact factor: 13.084

5.  Fluorinated Amine Stereotriads via Allene Amination.

Authors:  Lu Liu; Nels C Gerstner; Lucas J Oxtoby; Ilia A Guzei; Jennifer M Schomaker
Journal:  Org Lett       Date:  2017-06-02       Impact factor: 6.005

6.  Synthesis of α-Fluoro-α-Amino Acid Derivatives via Photoredox-Catalyzed Carbofluorination.

Authors:  Jaehoon Sim; Mark W Campbell; Gary A Molander
Journal:  ACS Catal       Date:  2019-01-24       Impact factor: 13.084

7.  Oxidative allene amination for the synthesis of nitrogen-containing heterocycles.

Authors:  Josephine Eshon; Nels C Gerstner; Jennifer M Schomaker
Journal:  ARKIVOC       Date:  2018-11-26       Impact factor: 1.140

Review 8.  Expanding beyond canonical metabolism: Interfacing alternative elements, synthetic biology, and metabolic engineering.

Authors:  Kevin B Reed; Hal S Alper
Journal:  Synth Syst Biotechnol       Date:  2017-12-19

Review 9.  Biochemistry of fluoroprolines: the prospect of making fluorine a bioelement.

Authors:  Vladimir Kubyshkin; Rebecca Davis; Nediljko Budisa
Journal:  Beilstein J Org Chem       Date:  2021-02-15       Impact factor: 2.883

10.  Synthesis and Diels-Alder Reactivity of 4-Fluoro-4-Methyl-4H-Pyrazoles.

Authors:  Nile S Abularrage; Brian J Levandowski; Ronald T Raines
Journal:  Int J Mol Sci       Date:  2020-05-31       Impact factor: 5.923

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