The Cu(I)-catalyzed alkyne-azide cycloaddition (CuAAC) has become increasingly important in the conjugation chemistry of biomolecules. For example, it is an efficient and convenient method to generate defined ubiquitin-protein conjugates. Here, we investigate the effect of surfactants on the efficiency of CuAAC for chemical protein ubiquitylation. We found that anionic surfactants enhance conjugate formation by up to 10-fold resulting in high yields even at low (i.e., micromolar) concentrations of the reactants. Notably, the herein investigated conjugates are functional and thus properly folded.publishe
The efficient bioconjugation of functional groups/molecules to targeted matrix and bio-related speci...
This document is the unedited Author’s version of a Submitted Work that was subsequently accepted fo...
Considerable attention has been focused on improving the biocompatibility of Cu(I)-catalyzed azide-a...
reaction—the most widely recognized example of click chemistry[2]—has been rapidly embraced for appl...
The application of click chemistry, specifically Copper-Catalyzed Azide-Alkyne Cycloaddition (CuAAC)...
Bioorthogonal conjugation reactions such as strain-promoted azide–alkyne cycloaddition (SPAAC) have ...
For biomedical applications, proteins may require conjugation to small and large molecules. Typical ...
For biomedical applications, proteins may require conjugation to small and large molecules. Typical ...
Modification of proteins by the covalent attachment of ubiquitin (Ub) plays a fundamental role in th...
Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC) is an efficient reaction linking an azido and an ...
The Cu(I)-catalyzed azide−alkyne cycloaddition (CuAAC) has recently proven to be a powerful syntheti...
The modification of liposomal surfaces is of interest for many different applications and a variety ...
Bioorthogonal chemistry allows rapid and highly selective reactivity in biological environments. The...
Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC) is an efficient reaction linking an azido and an ...
The copper (I)-catalyzed alkyne azide 1,3-dipolar cycloaddition (CuAAC) or ‘click’ reaction, is a hi...
The efficient bioconjugation of functional groups/molecules to targeted matrix and bio-related speci...
This document is the unedited Author’s version of a Submitted Work that was subsequently accepted fo...
Considerable attention has been focused on improving the biocompatibility of Cu(I)-catalyzed azide-a...
reaction—the most widely recognized example of click chemistry[2]—has been rapidly embraced for appl...
The application of click chemistry, specifically Copper-Catalyzed Azide-Alkyne Cycloaddition (CuAAC)...
Bioorthogonal conjugation reactions such as strain-promoted azide–alkyne cycloaddition (SPAAC) have ...
For biomedical applications, proteins may require conjugation to small and large molecules. Typical ...
For biomedical applications, proteins may require conjugation to small and large molecules. Typical ...
Modification of proteins by the covalent attachment of ubiquitin (Ub) plays a fundamental role in th...
Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC) is an efficient reaction linking an azido and an ...
The Cu(I)-catalyzed azide−alkyne cycloaddition (CuAAC) has recently proven to be a powerful syntheti...
The modification of liposomal surfaces is of interest for many different applications and a variety ...
Bioorthogonal chemistry allows rapid and highly selective reactivity in biological environments. The...
Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC) is an efficient reaction linking an azido and an ...
The copper (I)-catalyzed alkyne azide 1,3-dipolar cycloaddition (CuAAC) or ‘click’ reaction, is a hi...
The efficient bioconjugation of functional groups/molecules to targeted matrix and bio-related speci...
This document is the unedited Author’s version of a Submitted Work that was subsequently accepted fo...
Considerable attention has been focused on improving the biocompatibility of Cu(I)-catalyzed azide-a...