Recent advances in optical nanoscopy have brought the imaging resolution to the size of the individual macromolecules, thereby setting stringent requirements for the fluorescent labels. Such requirements are optimally fulfilled by the incorporation of unnatural amino acids (UAAs) in the proteins of interest (POI), followed by fluorophore conjugation via click chemistry. However, this approach has been limited to single POIs in mammalian cells. Here we solve this problem by incorporating different UAAs in different POIs, which are expressed in independent cell sets. The cells are then fused, thereby combining the different proteins and organelles, and are easily imaged by dual-color super-resolution microscopy. This procedure, which we terme...
SummaryThe visualization of complex cellular processes involving multiple proteins requires the use ...
Fluorescence labeling of difficult to access protein sites, e.g., in confined compartments, requires...
Fluorophores have transformed the way we study biological systems, enabling non-invasive studies in ...
Recent advances in optical nanoscopy have brought the imaging resolution to the size of the individu...
Recent advances in optical nanoscopy have brought the imaging resolution to the size of the individu...
Genetic code expansion is emerging as an important tool for manipulation and labeling of proteins in...
The growing demands of advanced fluorescence and super-resolution microscopy benefit from the develo...
The advent of super-resolution microscopy (nanoscopy) has set high standards for fluorescence taggin...
We demonstrate high-density labelling of cellular DNA and RNA using click chemistry and perform conf...
Many biophysical techniques that are available to study the structure, function and dynamics of cell...
Fluorescence can be used in optical imaging to view cell activity in vivo. Fluorescent proteins and ...
Optical imaging using fluorescence is limited by fluorophore size and unsuitability for in vivo anal...
Twenty-five years ago, GFP revolutionized the field of cell biology by enabling scientists to visua...
Methods to site-specifically and densely label proteins in cellular ultrastructures with small, brig...
EM has long been the main technique for imaging cell structures with nanometer resolution but has la...
SummaryThe visualization of complex cellular processes involving multiple proteins requires the use ...
Fluorescence labeling of difficult to access protein sites, e.g., in confined compartments, requires...
Fluorophores have transformed the way we study biological systems, enabling non-invasive studies in ...
Recent advances in optical nanoscopy have brought the imaging resolution to the size of the individu...
Recent advances in optical nanoscopy have brought the imaging resolution to the size of the individu...
Genetic code expansion is emerging as an important tool for manipulation and labeling of proteins in...
The growing demands of advanced fluorescence and super-resolution microscopy benefit from the develo...
The advent of super-resolution microscopy (nanoscopy) has set high standards for fluorescence taggin...
We demonstrate high-density labelling of cellular DNA and RNA using click chemistry and perform conf...
Many biophysical techniques that are available to study the structure, function and dynamics of cell...
Fluorescence can be used in optical imaging to view cell activity in vivo. Fluorescent proteins and ...
Optical imaging using fluorescence is limited by fluorophore size and unsuitability for in vivo anal...
Twenty-five years ago, GFP revolutionized the field of cell biology by enabling scientists to visua...
Methods to site-specifically and densely label proteins in cellular ultrastructures with small, brig...
EM has long been the main technique for imaging cell structures with nanometer resolution but has la...
SummaryThe visualization of complex cellular processes involving multiple proteins requires the use ...
Fluorescence labeling of difficult to access protein sites, e.g., in confined compartments, requires...
Fluorophores have transformed the way we study biological systems, enabling non-invasive studies in ...