Super-resolution imaging prompts re-thinking of cell biology mechanisms: Selected cases using stimulated emission depletion microscopy

BioEssays

Volumn 34, Issue 5, 2012, Pages 386-395

  Saka, Sinem ^a,b   Rizzoli, Silvio O ^a  

^a Deutsche Forschungsgemeinschaft   (Germany)

^b INTERNATIONAL MAX PLANCK RESEARCH SCHOOL FOR MOLECULAR BIOLOGY   (Germany)

Author keywords

Image interpretation; Neuroimaging; Protein cluster; STED microscopy; Super resolution

Indexed keywords

SYNAPTOPHYSIN; SYNAPTOSOMAL ASSOCIATED PROTEIN 25; SYNAPTOTAGMIN; SYNTAXIN 1;

ACCURACY; ARTICLE; CELL FUNCTION; CELL MEMBRANE; CONCEPTUAL FRAMEWORK; CONFOCAL MICROSCOPY; CYTOLOGY; DESCRIPTIVE RESEARCH; ELECTRON MICROSCOPY; FLUORESCENCE MICROSCOPY; GENE MUTATION; MICROSCOPY; MOLECULAR SIZE; NEUROTRANSMITTER RELEASE; NONHUMAN; PROTEIN FOLDING; PROTEIN FUNCTION; PROTEIN INTERACTION; PROTEIN LOCALIZATION; PROTEIN PROTEIN INTERACTION; STIMULATED EMISSION DEPLETION MICROSCOPY; SYNAPSE VESICLE;

HUMANS; IMAGE INTERPRETATION, COMPUTER-ASSISTED; MICROSCOPY; MOLECULAR IMAGING; PHYSICAL PROCESSES; R-SNARE PROTEINS; SYNAPTOSOMAL-ASSOCIATED PROTEIN 25; SYNTAXIN 1;

EID: 84859856039     PISSN: 02659247     EISSN: 15211878     Source Type: Journal    
DOI: 10.1002/bies.201100080     Document Type: Article

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