Inter-Dye Distance Distributions Studied by a Combination of Single-Molecule FRET-Filtered Lifetime Measurements and a Weighted Accessible Volume (wAV) Algorithm

Förster resonance energy transfer (FRET) is an important tool for studying the structural and dynamical properties of biomolecules. The fact that both the internal dynamics of the biomolecule and the movements of the biomolecule-attached dyes can occur on similar timescales of nanoseconds is an inherent problem in FRET studies. By performing single-molecule FRET-filtered lifetime measurements, we are able to characterize the amplitude of the motions of fluorescent probes attached to double-stranded DNA standards by means of flexible linkers. With respect to previously proposed experimental approaches, we improved the precision and the accuracy of the inter-dye distance distribution parameters by filtering out the donor-only population with pulsed interleaved excitation. A coarse-grained model is employed to reproduce the experimentally determined inter-dye distance distributions. This approach can easily be extended to intrinsically flexible proteins allowing, under certain conditions, to decouple the macromolecule amplitude of motions from the contribution of the dye linkers.

[1]  J M Beechem,et al.  Global analysis of biochemical and biophysical data. , 1992, Methods in enzymology.

[2]  J. Fisz Fluorescence polarization spectroscopy at combined high-aperture excitation and detection: application to one-photon-excitation fluorescence microscopy. , 2007, The journal of physical chemistry. A.

[3]  Giridharan Gokulrangan,et al.  Orientational dynamics and dye-DNA interactions in a dye-labeled DNA aptamer. , 2005, Biophysical journal.

[4]  Jeremy C. Smith,et al.  Fluorescence quenching of dyes by tryptophan: interactions at atomic detail from combination of experiment and computer simulation. , 2003, Journal of the American Chemical Society.

[5]  B. Schuler,et al.  Unfolded protein and peptide dynamics investigated with single-molecule FRET and correlation spectroscopy from picoseconds to seconds. , 2008, The journal of physical chemistry. B.

[6]  Kai Zhang,et al.  Photon-by-photon determination of emission bursts from diffusing single chromophores. , 2005, The journal of physical chemistry. B.

[7]  H. Grubmüller,et al.  Structural Heterogeneity and Quantitative FRET Efficiency Distributions of Polyprolines through a Hybrid Atomistic Simulation and Monte Carlo Approach , 2011, PloS one.

[8]  C. Bustamante,et al.  Overstretching B-DNA: The Elastic Response of Individual Double-Stranded and Single-Stranded DNA Molecules , 1996, Science.

[9]  C. Seidel,et al.  Triphosphate induced dimerization of human guanylate binding protein 1 involves association of the C-terminal helices: a joint double electron-electron resonance and FRET study. , 2014, Biochemistry.

[10]  John R. Wolberg Data Analysis Using the Method of Least Squares , 2013 .

[11]  Jens Michaelis,et al.  A nano-positioning system for macromolecular structural analysis , 2008, Nature Methods.

[12]  Christoph Bräuchle,et al.  Pulsed interleaved excitation. , 2005, Biophysical journal.

[13]  Michael Wahl,et al.  Time-Correlated Single Photon Counting , 2009 .

[14]  H. Grubmüller,et al.  Simulation of fluorescence anisotropy experiments: probing protein dynamics. , 2005, Biophysical journal.

[15]  E. Katchalski‐Katzir,et al.  Distribution of end-to-end distances of oligopeptides in solution as estimated by energy transfer. , 1975, Proceedings of the National Academy of Sciences of the United States of America.

[16]  E. Haas,et al.  Domain motions in phosphoglycerate kinase: determination of interdomain distance distributions by site-specific labeling and time-resolved fluorescence energy transfer. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[17]  Alexandre M. J. J. Bonvin,et al.  3D-DART: a DNA structure modelling server , 2009, Nucleic Acids Res..

[18]  J M Beechem,et al.  Simultaneous determination of intramolecular distance distributions and conformational dynamics by global analysis of energy transfer measurements. , 1989, Biophysical journal.

[19]  J. Lakowicz Principles of fluorescence spectroscopy , 1983 .

[20]  Christian Eggeling,et al.  Quantitative identification of different single molecules by selective time-resolved confocal fluorescence spectroscopy. , 1998 .

[21]  M. Sanborn,et al.  Fluorescence properties and photophysics of the sulfoindocyanine Cy3 linked covalently to DNA. , 2007, The journal of physical chemistry. B.

[22]  A Grinvald,et al.  Evaluation of the distribution of distances between energy donors and acceptors by fluorescence decay. , 1972, Proceedings of the National Academy of Sciences of the United States of America.

[23]  A. Szabó,et al.  Single-molecule FRET with diffusion and conformational dynamics. , 2007, The journal of physical chemistry. B.

[24]  Th. Förster Zwischenmolekulare Energiewanderung und Fluoreszenz , 1948 .

[25]  Claus A M Seidel,et al.  A toolkit and benchmark study for FRET-restrained high-precision structural modeling , 2012, Nature Methods.

[26]  H. Scheraga,et al.  Conformational unfolding in the N-terminal region of ribonuclease A detected by nonradiative energy transfer. , 1986, Biochemistry.

[27]  Shimon Weiss,et al.  Shot-noise limited single-molecule FRET histograms: comparison between theory and experiments. , 2006, The journal of physical chemistry. B.

[28]  P. Kapusta,et al.  Instrument response standard in time-resolved fluorescence. , 2009, The Review of scientific instruments.

[29]  Irina V Gopich Concentration effects in "single-molecule" spectroscopy. , 2008, The journal of physical chemistry. B.

[30]  C. Seidel,et al.  Accurate single-molecule FRET studies using multiparameter fluorescence detection. , 2010, Methods in enzymology.

[31]  Helmut Grubmüller,et al.  Single-molecule FRET measures bends and kinks in DNA , 2008, Proceedings of the National Academy of Sciences.

[32]  Suren Felekyan,et al.  On the origin of broadening of single-molecule FRET efficiency distributions beyond shot noise limits. , 2010, The journal of physical chemistry. B.

[33]  Sabine Müller,et al.  Accurate distance determination of nucleic acids via Förster resonance energy transfer: implications of dye linker length and rigidity. , 2011, Journal of the American Chemical Society.

[34]  R. Winkler,et al.  Conformational state distributions and catalytically relevant dynamics of a hinge-bending enzyme studied by single-molecule FRET and a coarse-grained simulation. , 2014, Biophysical journal.

[35]  P. Kapusta,et al.  Evaluation of instrument response functions for lifetime imaging detectors using quenched Rose Bengal solutions , 2009 .

[36]  W. Webb,et al.  Mechanisms of quenching of Alexa fluorophores by natural amino acids. , 2010, Journal of the American Chemical Society.

[37]  J. Beechem,et al.  Design and characterization of a multisite fluorescence energy-transfer system for protein folding studies: a steady-state and time-resolved study of yeast phosphoglycerate kinase. , 1997, Biochemistry.

[38]  W. Eaton,et al.  Characterizing the unfolded states of proteins using single-molecule FRET spectroscopy and molecular simulations , 2007, Proceedings of the National Academy of Sciences.