Results 21 to 30 of about 2,845,268 (289)

Unnatural amino acid incorporation in E. coli: current and future applications in the design of therapeutic proteins.

open access: yesFrontiers in Chemistry, 2014
Unnatural amino acid (UAA) incorporation by amber codon suppression offers scientists a powerful tool to modify the properties of proteins at will. UAA incorporation has been used for a plethora of fundamental research applications and, more recently ...
Huib eOvaa, kim ewals
doaj   +1 more source

Structure-Function Studies of Nicotinic Acetylcholine Receptors Using Unnatural Amino Acids [PDF]

open access: yes, 2012
This dissertation primarily describes structure-function studies of the nicotinic acetylcholine receptors (nAChRs). These studies use a combination of unnatural amino acid mutagenesis and electrophysiology to determine the specific molecular interactions
Puskar, Nyssa Leigh
core   +1 more source

Bicyclic Pyrrolidine-Isoxazoline γ Amino Acid: A Constrained Scaffold for Stabilizing α-Turn Conformation in Isolated Peptides

open access: yesFrontiers in Chemistry, 2019
Unnatural amino acids have tremendously expanded the folding possibilities of peptides and peptide mimics. While α,α-disubstituted and β-amino acids are widely studied, γ-derivatives have been less exploited.
Francesco Oliva   +5 more
doaj   +1 more source

Evaluation and optimisation of unnatural amino acid incorporation and bioorthogonal bioconjugation for site-specific fluorescent labelling of proteins expressed in mammalian cells

open access: yesBiochemistry and Biophysics Reports, 2019
Many biophysical techniques that are available to study the structure, function and dynamics of cellular constituents require modification of the target molecules.
Leonhard Jakob   +2 more
doaj   +1 more source

Site-Specific Antibody Conjugation with Payloads beyond Cytotoxins

open access: yesMolecules, 2023
As antibody–drug conjugates have become a very important modality for cancer therapy, many site-specific conjugation approaches have been developed for generating homogenous molecules.
Qun Zhou
doaj   +1 more source

Activation of Prp28 ATPase by phosphorylated Npl3 at a critical step of spliceosome remodeling

open access: yesNature Communications, 2021
Yeast helicase Prp28 promotes the first step of spliceosome remodeling. By placing a photoactivatable unnatural amino acid in Prp28, the authors capture Prp28 in action revealing its dynamic interactions and cofactor Npl3.
Fu-Lung Yeh   +12 more
doaj   +1 more source

Antimicrobial Activity of Amino Acid Analogues and Their Derivatives

open access: yesProceedings, 2017
Libraries of compounds containing unnatural amino acids or amino acid analogues were prepared from inexpensive substrates using sustainable processes [1–3]. [...]
Dácil Hernández   +4 more
doaj   +1 more source

Enzymatic aminoacylation of tRNA with unnatural amino acids [PDF]

open access: yesProceedings of the National Academy of Sciences, 2006
The biochemical flexibility of the cellular translation apparatus offers, in principle, a simple route to the synthesis of drug-like modified peptides and novel biopolymers. However, only ≈75 unnatural building blocks are known to be fully compatible with enzymatic tRNA acylation and subsequent ribosomal synthesis of modified ...
Matthew C T, Hartman   +2 more
openaire   +2 more sources

Synthesis of Both Enantiomers of Chiral Phenylalanine Derivatives Catalyzed by Cinchona Alkaloid Quaternary Ammonium Salts as Asymmetric Phase Transfer Catalysts

open access: yesMolecules, 2018
A practical synthesis of both enantiomers of unnatural phenylalanine derivatives by using two pseudoenantiomeric phase transfer catalysts is described.
Lei Jin, Shuai Zhao, Xin Chen
doaj   +1 more source

A New Unnatural Amino Acid Derived from the Modification of 4′-(p-tolyl)-2,2′:6′,2″-terpyridine and Its Mixed-Ligand Complexes with Ruthenium: Synthesis, Characterization, and Photophysical Properties

open access: yesChemistry, 2023
The modification of the methyl group of 4′-(p-tolyl)-2,2′:6′,2″-terpyridine produced the novel unnatural amino acid 3-(4-([2,2′:6′,2″-terpyridin]-4′-yl)phenyl)-2-aminopropanoic acid (phet).
Konstantinos Ypsilantis   +5 more
doaj   +1 more source

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