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Multicolor Fluorescence Nanoscopy by Photobleaching : Concept Verification and its Application to Resolve Selective Storage of Proteins in Platelets

Rönnlund, Daniel, 1984- (författare)
KTH,Experimentell biomolekylär fysik
Xu, Lei (författare)
KTH,Experimentell biomolekylär fysik
Perols, Anna (författare)
KTH,Proteinteknologi
visa fler...
Eriksson Karlström, Amelie (författare)
KTH,Proteinteknologi
Auer, Gert (författare)
Karolinska Institutet
Widengren, Jerker (författare)
KTH,Experimentell biomolekylär fysik
Gad, AKB (författare)
Karolinska Institutet
visa färre...
 (creator_code:org_t)
2014-04-24
2014
Engelska.
Ingår i: ACS Nano. - : American Chemical Society (ACS). - 1936-0851 .- 1936-086X. ; 8:5, s. 4358-4365
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Fluorescence nanoscopy provides means to discernthe finer details of protein localization and interaction in cells by offeringan order of magnitude higher resolution than conventional optical imagingtechniques. However, these super resolution techniques put higher demands onthe optical system as well as on the fluorescent probes, making multicolorfluorescence nanoscopy a challenging task. Here we present a new and simpleprocedure which exploits the photostability and excitation spectra of dyes toincrease the number of simultaneous recordable targets in STED nanoscopy. Weuse this procedure to demonstrate four color STED imaging of platelets with ≤40 nm resolution and low crosstalk. Platelets can selectively store, sequesterand release a multitude of different proteins, and in a manner specific fordifferent physiological and disease states. By applying multicolor nanoscopy tostudy platelets, we can achieve spatial mapping of the protein organizationwith a high resolution, for multiple proteins at the same time and in the samecell. This provides a means to identify specific platelet activation states fordiagnostic purposes and to understand the underlying protein storage andrelease mechanisms. We studied the organization of the pro- and anti-angiogenicproteins VEGF and PF-4 together with fibrinogen and filamentous actin, andfound distinct features in their respective protein localization. Further,colocalization analysis revealed only minor overlap between the proteins VEGFand PF-4 indicating that they have separate storage and release mechanisms,corresponding well with their opposite rules as pro- and anti-angiogenicproteins, respectively.

Ämnesord

NATURVETENSKAP  -- Fysik (hsv//swe)
NATURAL SCIENCES  -- Physical Sciences (hsv//eng)

Nyckelord

multicolor
super resolution microscopy
photobleaching
STED
platelets
thrombocytes
α-granules
Biological Physics
Biologisk fysik

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