We present a microfluidic platform for studying structure-function relationships at the cellular level by connecting video rate live cell imaging with in situ microfluidic cryofixation and cryo-electron tomography of near natively preserved, unstained specimens. Correlative light and electron microscopy (CLEM) has been limited by the time required to transfer live cells from the light microscope to dedicated cryofixation instruments, such as a plunge freezer or high-pressure freezer. We recently demonstrated a microfluidic based approach that enables sample cryofixation directly in the light microscope with millisecond time resolution, a speed improvement of up to three orders of magnitude. Here we show that this cryofixation method can be ...
The development of cryo-focused ion beam (cryo-FIB) for the thinning of frozen-hydrated biological s...
Cryo-electron tomography (CET) is a well-established technique for imaging cellular and molecular st...
The desire to study macromolecular complexes within their cellular context requires the ability to p...
We present a microfluidic platform for studying structure-function relationships at the cellular lev...
Cryofixation yields outstanding ultrastructural preservation of cells for electron microscopy, but c...
Light and electron microscopy are complementary methods to study biological systems at the cellular ...
Correlating live‐cell imaging with electron microscopy is among the most promising approaches to rel...
Cryofixation yields outstanding ultrastructural preservation of cells for electron microscopy, but c...
Cryo-electron tomography (cryo-ET) is a groundbreaking technology for 3D visualisation and analysis ...
AbstractCryo-electron tomography (cryo-ET) provides great insights into the ultrastructure of cells ...
Cryo-electron tomography provides 3D views of cellular architecture with molecular resolution. A pri...
Cryo-electron tomography provides 3D views of cellular architecture with molecular resolution. A pri...
The preservation of cells for electron microscopy by chemical fixation is a lengthy process, requiri...
Cryogenic electron tomography (cryo-ET) combined with sub-tomogram averaging, allows in-situ visuali...
The development of cryo-focused ion beam (cryo-FIB) for the thinning of frozen-hydrated biological s...
The development of cryo-focused ion beam (cryo-FIB) for the thinning of frozen-hydrated biological s...
Cryo-electron tomography (CET) is a well-established technique for imaging cellular and molecular st...
The desire to study macromolecular complexes within their cellular context requires the ability to p...
We present a microfluidic platform for studying structure-function relationships at the cellular lev...
Cryofixation yields outstanding ultrastructural preservation of cells for electron microscopy, but c...
Light and electron microscopy are complementary methods to study biological systems at the cellular ...
Correlating live‐cell imaging with electron microscopy is among the most promising approaches to rel...
Cryofixation yields outstanding ultrastructural preservation of cells for electron microscopy, but c...
Cryo-electron tomography (cryo-ET) is a groundbreaking technology for 3D visualisation and analysis ...
AbstractCryo-electron tomography (cryo-ET) provides great insights into the ultrastructure of cells ...
Cryo-electron tomography provides 3D views of cellular architecture with molecular resolution. A pri...
Cryo-electron tomography provides 3D views of cellular architecture with molecular resolution. A pri...
The preservation of cells for electron microscopy by chemical fixation is a lengthy process, requiri...
Cryogenic electron tomography (cryo-ET) combined with sub-tomogram averaging, allows in-situ visuali...
The development of cryo-focused ion beam (cryo-FIB) for the thinning of frozen-hydrated biological s...
The development of cryo-focused ion beam (cryo-FIB) for the thinning of frozen-hydrated biological s...
Cryo-electron tomography (CET) is a well-established technique for imaging cellular and molecular st...
The desire to study macromolecular complexes within their cellular context requires the ability to p...