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Today’s take-home lessons: FRET (i. e
Today’s take-home lessons: FRET (i.e. what you should be able to answer at end of lecture) How to measure: Donor Intensity, Lifetime Acceptor Intensity (very good way but more difficult) Why is E.T. a to (R/Ro)-6 [it depends on the near-field component of the electric field, which goes like R-3 with some normalization constant Ro-3
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FRET: measuring conformational changes of biomolecules
FRET useful for 20-80Å Distance dependent interactions between green and red light bulbs can be used to deduce the shape of the scissors during the function.
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Fluorescence Resonance Energy Transfer (FRET)
Spectroscopic Ruler for measuring nm-scale distances, binding R (Å) E Ro 50 Å Energy Transfer Donor Acceptor Dipole-Dipole distant-dependent energy transfer Time Time Look at relative amounts of green & red
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Donor Intensity or Donor Lifetime
FRET Measured by Donor Intensity or Donor Lifetime Call the Donor Intensity ID , Lifetime tD Donor Intensity in the presence of Acceptor IDA , tDA E = 1 – IDA/ID E = 1 – tDA/tD In FRET, there is a drop in donor’s intensity and lifetime k = krad + kn.r. tD = 1/k = trad + tn.r. QY = krad/(krad + kn.r) k = krad + kn.r. + kFRET tDA = 1/k = trad + tn.r + tFRET QY = krad/(krad + kn.r + kFRET)
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Example of FRET What is the end-to-end distance on a dsDNA?
D= Fluorescein A = Tetramethylrhodamine
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Example of FRET (on DNA)
E.T. by decreases in donor emission. Need to compare two samples, d-only, and D-A. Where are the donors intensity, and excited state lifetime in the presence of acceptor; without the acceptor. Donor quenching Acceptor “sensitized” emission The more Energy Transfer (donor and acceptor closer together)… more donor decreases, more the acceptor increases.
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Example of FRET (on DNA)
Donor quenching Acceptor “sensitized” emission What if the acceptor doesn’t fluoresce? Is E=0? (It has a quantum yield of fluorescence = 0) But it accepts just fine (Absorption is normal) No! Sensitized emission = 0, but donor quenching still happens
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Example of FRET (on DNA) Measured w Acceptor’s Sensitized Emission
E.T. by increase in acceptor fluorescence and compare it to residual donor emission. Need to compare one sample at two l and also measure their quantum yields. Ideal case, where direct acceptor’s emission = 0 (Next slide, subtract it off) Donor quenching Acceptor “sensitized” emission Energy Transfer (E) is an indication of excitations, not emission. Must divide by quantum yields.
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Example of FRET (on DNA) Measured w Acceptor’s Sensitized Emission
Real case, where direct acceptor’s emission ≠ 0. How to subtract it off? Donor quenching Acceptor “sensitized” emission [Below not discussed in lecture] Use two lasers, one to induce FRET, the other where only the acceptor excites. (e.g. 488 nm for Fl: 532 nm for TMR: see next slide) Then take an acceptor-only sample, excite at the two wavelengths and multiply by the ratio of the acceptors absorption at these two wavelengths.
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Why does E.T. go like (R/Ro)-6
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E.T. a 1/R6 :How is kET dependent on R?
How does the energy go with distance? Think of a source emitting and look at R1, then 2R1, 3R1. U ≈1/R2 (Traveling: photons) How does electric field go like? U ≈ E2 ; E ≈ 1/R This is in the “Far-field”: (d >> l) In the Near-field (d << l) (must remember your E&M) E ≈1/R3 peE = pe/R3 Dipole emitting: Energy = U = Dipole absorption: paE Probability that absorbing molecule (dipole) absorbs the light So light emission goes like paE x peE = papeE2, pepa/R6 ≈ E.T. So (classically) E.T. goes like R-6 and pepa ~ Ro6 (a constant with right units) E.T. =1/(1 +knd/kET) = 1/(1 + (R6/Ro6)) = 1/(1 + 1/kETtD)
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