Schizosaccharomyces pombe is an outstanding model organism for cell biological investigations, yet the range of useful and well-characterized fluorescent proteins (XFPs) is limited. We generated and characterized three recoded fluorescent proteins for 3-color analysis in S.pombe, Super-folder GFP, monomeric Kusabira Orange 2 and E2Crimson. Upon optimization and expression in S. pombe, the three proteins enabled sensitive simultaneous 3-color detection capability. Furthermore, we describe a strategy that combines a pulse-chase approach and mathematical modeling to quantify the maturation kinetics of these proteins in vivo. We observed maturation kinetics in S. pombe that are expected from those described for these proteins in vitro and/or in...
Microscopy of fluorescently labeled proteins has become a standard technique for live cell imaging. ...
In this work, we have developed an expansion microscopy (ExM) protocol that combines ExM with photoa...
In this work, we have developed an expansion microscopy (ExM) protocol that combines ExM with photoa...
Schizosaccharomyces pombe is an outstanding model organism for cell biological investigations, yet t...
<div><p><i>Schizosaccharomyces pombe</i> is an outstanding model organism for cell biological invest...
Fluorescent protein (FP) maturation can limit the accuracy with which dynamic intracellular processe...
Saccharomyces cerevisiae are widely used for imaging fluorescently tagged protein fusions. Fluoresce...
Saccharomyces cerevisiae are widely used for imaging fluorescently tagged protein fusions. Fluoresce...
Fluorescent proteins (FPs) are widely used in many organisms, but are commonly characterised in vitr...
Time-lapse imaging of live cells using multiple fluorescent reporters is an essential tool to study ...
In this work, we have developed an expansion microscopy (ExM) protocol that combines ExM with photoa...
Summary: Microscopy-based analysis of protein accumulation at a given subcellular location in real t...
AbstractTagging expressed proteins with the green fluorescent protein (GFP) from Aequorea victoria[1...
In this work, we have developed an expansion microscopy (ExM) protocol that combines ExM with photoa...
Next-generation sequencing approaches have considerably advanced our understanding of genome functio...
Microscopy of fluorescently labeled proteins has become a standard technique for live cell imaging. ...
In this work, we have developed an expansion microscopy (ExM) protocol that combines ExM with photoa...
In this work, we have developed an expansion microscopy (ExM) protocol that combines ExM with photoa...
Schizosaccharomyces pombe is an outstanding model organism for cell biological investigations, yet t...
<div><p><i>Schizosaccharomyces pombe</i> is an outstanding model organism for cell biological invest...
Fluorescent protein (FP) maturation can limit the accuracy with which dynamic intracellular processe...
Saccharomyces cerevisiae are widely used for imaging fluorescently tagged protein fusions. Fluoresce...
Saccharomyces cerevisiae are widely used for imaging fluorescently tagged protein fusions. Fluoresce...
Fluorescent proteins (FPs) are widely used in many organisms, but are commonly characterised in vitr...
Time-lapse imaging of live cells using multiple fluorescent reporters is an essential tool to study ...
In this work, we have developed an expansion microscopy (ExM) protocol that combines ExM with photoa...
Summary: Microscopy-based analysis of protein accumulation at a given subcellular location in real t...
AbstractTagging expressed proteins with the green fluorescent protein (GFP) from Aequorea victoria[1...
In this work, we have developed an expansion microscopy (ExM) protocol that combines ExM with photoa...
Next-generation sequencing approaches have considerably advanced our understanding of genome functio...
Microscopy of fluorescently labeled proteins has become a standard technique for live cell imaging. ...
In this work, we have developed an expansion microscopy (ExM) protocol that combines ExM with photoa...
In this work, we have developed an expansion microscopy (ExM) protocol that combines ExM with photoa...