Engineering pyrrolysine systems for genetic code expansion and reprogramming

DL Dunkelmann, JW Chin - Chemical Reviews, 2024 - ACS Publications
Over the past 16 years, genetic code expansion and reprogramming in living organisms has
been transformed by advances that leverage the unique properties of pyrrolysyl-tRNA …

Chemical protein modification through cysteine

SB Gunnoo, A Madder - ChemBioChem, 2016 - Wiley Online Library
The modification of proteins with non‐protein entities is important for a wealth of
applications, and methods for chemically modifying proteins attract considerable attention …

Designing logical codon reassignment–Expanding the chemistry in biology

A Dumas, L Lercher, CD Spicer, BG Davis - Chemical science, 2015 - pubs.rsc.org
Over the last decade, the ability to genetically encode unnatural amino acids (UAAs) has
evolved rapidly. The programmed incorporation of UAAs into recombinant proteins relies on …

Selective chemical protein modification

CD Spicer, BG Davis - Nature communications, 2014 - nature.com
Chemical modification of proteins is an important tool for probing natural systems, creating
therapeutic conjugates and generating novel protein constructs. Site-selective reactions …

Pyrrolysyl-tRNA synthetase: an ordinary enzyme but an outstanding genetic code expansion tool

W Wan, JM Tharp, WR Liu - Biochimica et Biophysica Acta (BBA)-Proteins …, 2014 - Elsevier
The genetic incorporation of the 22nd proteinogenic amino acid, pyrrolysine (Pyl) at amber
codon is achieved by the action of pyrrolysyl-tRNA synthetase (PylRS) together with its …

Histones: at the crossroads of peptide and protein chemistry

MM Müller, TW Muir - Chemical reviews, 2015 - ACS Publications
1. INTRODUCTION In eukaryotic cells, inheritable information is stored in a nucleoprotein
complex referred to as chromatin. 1 This genome architecture serves two key purposes. On …

[HTML][HTML] Synthesis of modified proteins via functionalization of dehydroalanine

J Dadova, SRG Galan, BG Davis - Current opinion in chemical biology, 2018 - Elsevier
Highlights•Dha in proteins is easily and flexibly accessible under mild conditions.•Dha
reactivity is used in β, γ-C–S/Se/N/C bond-formation and allows 'zero scar'protein …

The green side of the moon: ecofriendly aspects of organoselenium chemistry

S Santoro, JB Azeredo, V Nascimento, L Sancineto… - Rsc Advances, 2014 - pubs.rsc.org
Organoselenium chemistry has proven to be a powerful tool for organic synthesis over
several decades. Nevertheless, the use of selenating reagents has often been limited by a …

Site-selective modification of peptide backbones

A Boto, CC González, D Hernández… - Organic Chemistry …, 2021 - pubs.rsc.org
The site-selective modification of peptide backbones allows an outstanding fine-tuning of
peptide conformation, folding ability, and physico-chemical and biological properties …

Dehydroamino acids: Chemical multi-tools for late-stage diversification

JW Bogart, AA Bowers - Organic & biomolecular chemistry, 2019 - pubs.rsc.org
α, β-Dehydroamino acids (dhAAs) are noncanonical amino acids that are found in a wide
array of natural products and can be easily installed into peptides and proteins. dhAAs …