The selective and fast labeling of proteins in living cells is a major challenge. Live-cell labeling techniques require a high specificity, high labeling density, and cell permeability of the tagging molecule to target the protein of interest. Here, we report on the site-specific, rapid and efficient labeling of endogenous and recombinant histidine-tagged proteins at distinct subcellular compartments using cell-penetrating multivalent chelator carrier complexes. In vivo labeling was followed in real-time in living cells, demonstrating a high specificity and high degree of colocalization in the crowded cellular environment
Extracellular vesicles (EVs) are thought to mediate intercellular communication through the delivery...
International audienceThe use of the semiconductor quantum dots (QD) as biolabels for both ensemble ...
Chemical tags are now viable alternatives to fluorescent proteins for labeling proteins in living ce...
The selective and fast labeling of proteins in living cells is a major challenge. Live-cell labeling...
Selective and fast labeling of proteins in living cells is a major challenge. Live-cell labeling tec...
Live-cell labelling techniques to visualize proteins with minimal disturbance are important; however...
Small molecule-based fluorescent probes have been used for realtime visualization of live cells and ...
Accurate labeling of endogenous proteins for advanced light microscopy in living cells remains chall...
Background In the high-resolution microscopy era, genetic code expansion (GCE)-based bioorthogonal ...
AbstractGenetically encoded fluorescent labels, such as green fluorescent protein, make it possible ...
The cell cytosol is crowded with high concentrations of many different biomacromolecules, which is d...
Understanding the dynamic roles that proteins play in cell biology requires tools to selectively lab...
Chemical proteomics relies primarily on click-chemistry-based protein labeling and biotin-streptavid...
SummaryThe visualization of complex cellular processes involving multiple proteins requires the use ...
Wombacher R, Heidbreder M, van de Linde S, et al. Live-cell super-resolution imaging with trimethopr...
Extracellular vesicles (EVs) are thought to mediate intercellular communication through the delivery...
International audienceThe use of the semiconductor quantum dots (QD) as biolabels for both ensemble ...
Chemical tags are now viable alternatives to fluorescent proteins for labeling proteins in living ce...
The selective and fast labeling of proteins in living cells is a major challenge. Live-cell labeling...
Selective and fast labeling of proteins in living cells is a major challenge. Live-cell labeling tec...
Live-cell labelling techniques to visualize proteins with minimal disturbance are important; however...
Small molecule-based fluorescent probes have been used for realtime visualization of live cells and ...
Accurate labeling of endogenous proteins for advanced light microscopy in living cells remains chall...
Background In the high-resolution microscopy era, genetic code expansion (GCE)-based bioorthogonal ...
AbstractGenetically encoded fluorescent labels, such as green fluorescent protein, make it possible ...
The cell cytosol is crowded with high concentrations of many different biomacromolecules, which is d...
Understanding the dynamic roles that proteins play in cell biology requires tools to selectively lab...
Chemical proteomics relies primarily on click-chemistry-based protein labeling and biotin-streptavid...
SummaryThe visualization of complex cellular processes involving multiple proteins requires the use ...
Wombacher R, Heidbreder M, van de Linde S, et al. Live-cell super-resolution imaging with trimethopr...
Extracellular vesicles (EVs) are thought to mediate intercellular communication through the delivery...
International audienceThe use of the semiconductor quantum dots (QD) as biolabels for both ensemble ...
Chemical tags are now viable alternatives to fluorescent proteins for labeling proteins in living ce...