Switchable fluorophores for single-molecule localization microscopy
H Li, JC Vaughan - Chemical reviews, 2018 - ACS Publications
The past decade has witnessed an explosion in the use of super-resolution fluorescence
microscopy methods in biology and other fields. Single-molecule localization microscopy …
microscopy methods in biology and other fields. Single-molecule localization microscopy …
Fluorescent proteins for live-cell imaging with super-resolution
K Nienhaus, GU Nienhaus - Chemical Society Reviews, 2014 - pubs.rsc.org
Fluorescent proteins (FPs) from the GFP family have become indispensable as marker tools
for imaging live cells, tissues and entire organisms. A wide variety of these proteins have …
for imaging live cells, tissues and entire organisms. A wide variety of these proteins have …
Characterization and development of photoactivatable fluorescent proteins for single-molecule–based superresolution imaging
S Wang, JR Moffitt, GT Dempsey… - Proceedings of the …, 2014 - National Acad Sciences
Photoactivatable fluorescent proteins (PAFPs) have been widely used for superresolution
imaging based on the switching and localization of single molecules. Several properties of …
imaging based on the switching and localization of single molecules. Several properties of …
Photocontrollable fluorescent proteins for superresolution imaging
DM Shcherbakova, P Sengupta… - Annual review of …, 2014 - annualreviews.org
Superresolution fluorescence microscopy permits the study of biological processes at scales
small enough to visualize fine subcellular structures that are unresolvable by traditional …
small enough to visualize fine subcellular structures that are unresolvable by traditional …
Fluorescent proteins: shine on, you crazy diamond
P Dedecker, FC De Schryver… - Journal of the American …, 2013 - ACS Publications
In this Perspective we discuss recent trends in the development and applications of
fluorescent proteins. We start by providing a historical and structural perspective of their …
fluorescent proteins. We start by providing a historical and structural perspective of their …
[HTML][HTML] Photoswitchable fluorescent proteins: ten years of colorful chemistry and exciting applications
Highlights•Photoswitchable fluorescent proteins cycle between on and off states in response
to light.•Structural studies reveal diversity in the details of photoswitching …
to light.•Structural studies reveal diversity in the details of photoswitching …
Chemistry of photosensitive fluorophores for single-molecule localization microscopy
FM Jradi, LD Lavis - ACS Chemical Biology, 2019 - ACS Publications
Development of single-molecule localization microscopy (SMLM) has sparked a revolution
in biological imaging, allowing “super-resolution” fluorescence microscopy below the …
in biological imaging, allowing “super-resolution” fluorescence microscopy below the …
Membrane assembly of aquaporin-4 autoantibodies regulates classical complement activation in neuromyelitis optica
J Soltys, Y Liu, A Ritchie, S Wemlinger… - The Journal of …, 2019 - Am Soc Clin Investig
Neuromyelitis optica (NMO) is an autoimmune CNS disorder mediated by pathogenic
aquaporin-4 (AQP4) water channel autoantibodies (AQP4-IgG). Although AQP4-IgG–driven …
aquaporin-4 (AQP4) water channel autoantibodies (AQP4-IgG). Although AQP4-IgG–driven …
Superresolution imaging of biological systems using photoactivated localization microscopy
P Sengupta, SB Van Engelenburgˆ… - Chemical …, 2014 - ACS Publications
A progressive reduction of the spatial scale accessible by microscopes has catalyzed our
increasing understanding of cells and their constituents. Light microscopy has been at the …
increasing understanding of cells and their constituents. Light microscopy has been at the …
Three-dimensional super-resolution protein localization correlated with vitrified cellular context
We demonstrate the use of cryogenic super-resolution correlative light and electron
microscopy (csCLEM) to precisely determine the spatial relationship between proteins and …
microscopy (csCLEM) to precisely determine the spatial relationship between proteins and …