Temperature-cycle microscopy reveals single-molecule conformational heterogeneity
Author(s) -
Haifeng Yuan,
Alexander Gaiduk,
Joanna R. Siekierzycka,
Satoru Fujiyoshi,
Michio M. Matsushita,
Daniel Nettels,
Benjamin Schuler,
Claus A. M. Seidel,
Michel Orrit
Publication year - 2015
Publication title -
physical chemistry chemical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.053
H-Index - 239
eISSN - 1463-9084
pISSN - 1463-9076
DOI - 10.1039/c4cp05486e
Subject(s) - molecule , crystallography , chemistry , microscopy , materials science , chemical physics , physics , optics , organic chemistry
Our previous temperature-cycle study reported FRET transitions between different states on FRET-labeled polyprolines [Yuan et al., PCCP, 2011, 13, 1762]. The conformational origin of such transitions, however, was left open. In this work, we apply temperature-cycle microscopy of single FRET-labeled polyproline and dsDNA molecules and compare their responses to resolve the conformational origin of different FRET states. We observe different steady-state FRET distributions and different temperature-cycle responses in the two samples. Our temperature-cycle results on single molecules resemble the results in steady-state measurements but reveal a dark state which could not be observed otherwise. By comparing the timescales and probabilities of different FRET states in temperature-cycle traces, we assign the conformational heterogeneity reflected by different FRET states to linker dynamics, dye-chain and dye-dye interactions. The dark state and low-FRET state are likely due to dye-dye interactions at short separations.
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