Genetically encoded biosensors for visualizing live-cell biochemical activity at super-resolution

New fluorescent biosensors enable the first super-resolution imaging of enzyme activity in live cells via fluorescence fluctuation increase by contact (FLINC). Compartmentalized biochemical activities are essential to all cellular processes, but there is no generalizable method to visualize dynamic...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Nature methods 2017-04, Vol.14 (4), p.427-434
Hauptverfasser: Mo, Gary C H, Ross, Brian, Hertel, Fabian, Manna, Premashis, Yang, Xinxing, Greenwald, Eric, Booth, Chris, Plummer, Ashlee M, Tenner, Brian, Chen, Zan, Wang, Yuxiao, Kennedy, Eileen J, Cole, Philip A, Fleming, Karen G, Palmer, Amy, Jimenez, Ralph, Xiao, Jie, Dedecker, Peter, Zhang, Jin
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:New fluorescent biosensors enable the first super-resolution imaging of enzyme activity in live cells via fluorescence fluctuation increase by contact (FLINC). Compartmentalized biochemical activities are essential to all cellular processes, but there is no generalizable method to visualize dynamic protein activities in living cells at a resolution commensurate with cellular compartmentalization. Here, we introduce a new class of fluorescent biosensors that detect biochemical activities in living cells at a resolution up to threefold better than the diffraction limit. These 'FLINC' biosensors use binding-induced changes in protein fluorescence dynamics to translate kinase activities or protein–protein interactions into changes in fluorescence fluctuations, which are quantifiable through stochastic optical fluctuation imaging. A protein kinase A (PKA) biosensor allowed us to resolve minute PKA activity microdomains on the plasma membranes of living cells and to uncover the role of clustered anchoring proteins in organizing these activity microdomains. Together, these findings suggest that biochemical activities of the cell are spatially organized into an activity architecture whose structural and functional characteristics can be revealed by these new biosensors.
ISSN:1548-7091
1548-7105
DOI:10.1038/nmeth.4221