Fluorescence recovery after photobleaching was used to measure the diffusion coefficient of green fluorescent protein (GFP, 27 kDa) in Escherichia coli in the presence or absence of four coexpressed proteins: cytoplasmic maltose binding protein (42 kDa), tau-40 (45 kDa), α-synuclein (14 kDa), or calmodulin (17 kDa). The GFP diffusion coefficient remains constant regardless of the type of coexpresseed protein and whether or not the coexpressed protein was induced. We conclude that expression of these soluble proteins has little to no effect on the diffusion of GFP. These results have implications for the utility of in-cell nuclear magnetic resonance spectroscopy
In-cell nuclear magnetic resonance spectroscopy is a tool for studying proteins under physiologicall...
AbstractModulated fringe pattern photobleaching (MFPP) was used to measure the translational diffusi...
The effect of osmotic stress on the intracellular diffusion of proteins in Escherichia coli was stud...
Fluorescence recovery after photobleaching was used to measure the diffusion coefficient of green fl...
This dissertation describes the creation of a system to provide insight about the affects of protein...
The rate of protein diffusion in bacterial cytoplasm may constrain a variety of cellular functions a...
Diffusion in the bacterial cytoplasm is regarded as the primary method of intracellular protein move...
Surprisingly little is known about the physical environment inside a prokaryotic cell. Knowledge of ...
Fluorescence recovery after photobleaching and fluorescence correlation spectroscopy are the primary...
The characterization of molecules within a biologically relevant environment distinguishes nuclear m...
Background: Macromolecule mobility is often quantified with Fluorescence Recovery After Photobleachi...
Despite increased attention, little is known about how the crowded intracellular environment affects...
Inside prokaryotic cells, passive translational diffusion typically limits the rates with which cyto...
Inside prokaryotic cells, passive translational diffusion typically limits the rates with which cyto...
Intrinsically disordered proteins are important in signaling, regulation, and translocation. Underst...
In-cell nuclear magnetic resonance spectroscopy is a tool for studying proteins under physiologicall...
AbstractModulated fringe pattern photobleaching (MFPP) was used to measure the translational diffusi...
The effect of osmotic stress on the intracellular diffusion of proteins in Escherichia coli was stud...
Fluorescence recovery after photobleaching was used to measure the diffusion coefficient of green fl...
This dissertation describes the creation of a system to provide insight about the affects of protein...
The rate of protein diffusion in bacterial cytoplasm may constrain a variety of cellular functions a...
Diffusion in the bacterial cytoplasm is regarded as the primary method of intracellular protein move...
Surprisingly little is known about the physical environment inside a prokaryotic cell. Knowledge of ...
Fluorescence recovery after photobleaching and fluorescence correlation spectroscopy are the primary...
The characterization of molecules within a biologically relevant environment distinguishes nuclear m...
Background: Macromolecule mobility is often quantified with Fluorescence Recovery After Photobleachi...
Despite increased attention, little is known about how the crowded intracellular environment affects...
Inside prokaryotic cells, passive translational diffusion typically limits the rates with which cyto...
Inside prokaryotic cells, passive translational diffusion typically limits the rates with which cyto...
Intrinsically disordered proteins are important in signaling, regulation, and translocation. Underst...
In-cell nuclear magnetic resonance spectroscopy is a tool for studying proteins under physiologicall...
AbstractModulated fringe pattern photobleaching (MFPP) was used to measure the translational diffusi...
The effect of osmotic stress on the intracellular diffusion of proteins in Escherichia coli was stud...