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F luorescence Correlation Spectroscopy technique and its applications to DNA dynamics Oleg Krichevsky Ben-Gurion University in t he Negev. Outline. Tutorial on FCS The basic idea of the technique Instrumentation Standard applications: - measurements of concentrations
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Fluorescence Correlation Spectroscopy technique and its applications to DNA dynamics Oleg Krichevsky Ben-Gurion University in the Negev
Outline • Tutorial on FCS • The basic idea of the technique • Instrumentation • Standard applications: - measurements of concentrations - diffusion kinetics - binding assay • DNA dynamics
DNA hairpin • opening-closing kinetics to (k-) tc (k+) 2) DNA “breathing” 3) Polymer conformational dynamics - flexible polymers (ssDNA) - semi-flexible polymers (dsDNA) - semi-rigid polymers (F-actin)
Tools: • specific fluorescence labeling: • attaching fluorophores at precise positions • Fluorescence Correlation Spectroscopy (FCS)
t (ms) Fluorescence Correlation Spectroscopy (FCS) Magde, Elson & Webb (1972); Rigler et al (1993)
General Properties of FCS Correlation Function
Rh6G t (ms) Correlation function for simple diffusion:
Principles of confocal setup Sampling volume 0.5 fl (Ø 0.45 x 2 mm) Incident light power 10 - 50mW 0.1-300 molecules per sampling volume on average
Enhancements and variations of the standard setup: • Two-color FCS (Schwille et al) • Two-photon FCS (Berland et al) • Scanning FCS(Petersen et al) References and technical details in G. Bonnet and O.K., Reports on Progress in Physics, 65(2002), 251-297
Standard applications: • Amplitude of G(t)→ concentration of moving molecules • Decay → diffusion kinetics (in vitro and in vivo) • Binding assay
Fast Diffusion DNA + Few mm Slow Diffusion FCS as a Binding Assay Protein Few nm
In general, for two-component diffusion: Methyltransferase + Lambda-DNA (methyltransferase – courtesy of Albert Jeltsch and Vikas Handa)
DNA hairpin • opening-closing kinetics to (k-) tc (k+) with Grégore Altan-Bonnet Noel Goddard Albert Libchaber Rockefeller University
DNA hairpin fluctuations: Molecular beacon design Tyagi&Kramer (1996) to (k-) tc (k+) 5’ - Rh6G – CCCAA – (Xn) – TTGGG – [DABCYL] – 3’ (n=12-30) Signal/background:Io/ Ic ~ 50-100 I (kHz) T (oC)
FCS on Molecular beacons: two processes – two characteristic time scales
HOPE!!! Correlation function of a molecular beacon: G t (ms) structural fluctuations diffusion
to (k-) tc (k+) to (k-) tc (k+) Control: Beacon:
t (ms) Correlation functions of beacon & control Ratio of the correlation functions: pure conformational kinetics
Conformational kinetics at different temperatures: Gconf t (ms)
The experimental procedure: 1) Melting curves: I(T) I T 2) FCS on beacons: 3) FCS on controls:
Characteristic time scales of opening and closing of T21 loop hairpin:
The loops of equal length but different sequence: T21 vs. A21
Stacking interaction between bases
Closing enthalpy (kcal/mol) vs. loop length (poly-A) 0.55 kcal/mol/stacked base Opening and closing times of different poly-A loops
Placing a defect in a poly-A loop no defect PNAS 95, 8602-8606 (1998) Phys. Rev. Letters85, 2400-2403 (2000)
In some simple situations we have some understanding of the sequence-dependence of hairpin closing kinetics • In a number of other situations we have no undersanding • poly-C loops • short poly-T loops (below 7 bases(
2) DNA “breathing” The experimental construct:
Conformational dynamics of polymers in good solvents: on the model of dsDNA and ssDNA molecules
G(t) lag (ms) lag (ms) Diffusion of dsDNA 6700bp
Polymer Statistics Freely Jointed Chain model: Random Walks inSpace b Ree Ree
center of mass polymer end • The kinetics of monomer random motion: • double-stranded DNA (dsDNA) • single-stranded DNA (ssDNA) Polymer conformational dynamics: Rouse (1953) Zimm (1956)
Theory: b2 t
Basic length scale: b Basic timescale: Polymer size: N Rouse theory of Polymer Dynamics: b g
Mean-square displacement of an end-monomer: Center-of-mass internal Rouse modes: n 0 N
r Exact: Rouse model: connectivity + friction of polymer segments
1) Experimental measurements of polymer coil diffusion (dynamic light scattering) 2) Hydrodynamic interactions between polymer segments cannot be neglected Rouse model is nice but wrong:
Zimm model: Rouse model + hydrodynamic interactions Diverge with N => cannot be neglected even for distant monomers
Hydrodynamic shell: r Exact Zimm model: Rouse model + hydrodynamic interactions