FRET-enhanced photostability allows improved single-molecule tracking of proteins and protein complexes in live mammalian cells.

ABSTRACT: A major challenge in single-molecule imaging is tracking the dynamics of proteins or complexes for long periods of time in the dense environments found in living cells. Here, we introduce the concept of using FRET to enhance the photophysical properties of photo-modulatable (PM) fluorophores commonly used in such studies. By developing novel single-molecule FRET pairs, consisting of a PM donor fluorophore (either mEos3.2 or PA-JF₅₄₉) next to a photostable acceptor dye JF₆₄₆, we demonstrate that FRET competes with normal photobleaching kinetic pathways to increase the photostability of both donor fluorophores. This effect was further enhanced using a triplet-state quencher. Our approach allows us to significantly improve single-molecule tracking of chromatin-binding pr

SUBMITTER: Basu S 

PROVIDER: S-EPMC6023872 | biostudies-literature | 2018 Jun

REPOSITORIES: biostudies-literature