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Principles of Fluorescence Spectroscopy

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934 INDEX<br />

<strong>Fluorescence</strong> correlation spectroscopy [cont'd]<br />

total internal reflection, 821–822<br />

with two-photon excitation, 822–823<br />

diffusion <strong>of</strong> intracellular kinase, 823<br />

<strong>Fluorescence</strong> in-situ hybridization (FISH), 727–730<br />

applications <strong>of</strong>, 729–730<br />

preparation <strong>of</strong> probe DNA, 728–729<br />

spectral karyotyping, 730–732<br />

<strong>Fluorescence</strong> intensity distribution analysis, 817–819<br />

<strong>Fluorescence</strong> lifetime imaging microscopy (FLM), 97–98, 630, 741–752<br />

calcium concentration from lifetime, 744–745<br />

cos cells images, 745–746<br />

early methods for, 743–744<br />

frequency-domain laser scanning microscopy, 750–751<br />

literature references, 754<br />

laser scanning TCSPC film, 748–750<br />

images <strong>of</strong> amyloid plaques, 750<br />

literature references, 754<br />

literature references, 753–755<br />

using gated-image intensifier, 747–748<br />

wide-field frequency-domain film, 746–747<br />

imaging cells containing GFPs, 747<br />

laser scanning TCSPC film <strong>of</strong> cellular biomolecules, 750<br />

protein kinase C activation, 746–747<br />

<strong>Fluorescence</strong> microscopy, filters for, 41<br />

<strong>Fluorescence</strong> polarization. See Polarization<br />

<strong>Fluorescence</strong>-polarization immunoassays (FPIs), 661–663, 691–692<br />

<strong>Fluorescence</strong> quenching. See Quenching<br />

<strong>Fluorescence</strong> recovery after photobleaching, 814–815<br />

<strong>Fluorescence</strong> resonance energy transfer (FRET), 443. See also<br />

Energy transfer<br />

<strong>Fluorescence</strong> scanning spectroscopy<br />

theory <strong>of</strong>, 839<br />

<strong>Fluorescence</strong> standards. See Standards<br />

Fluorogenic probes, 79–80<br />

Fluorophore blinking, 767, 768, 769<br />

Fluorophores, 1, 63–95<br />

anisotropy decay, time-dependent, 391<br />

anisotropy <strong>of</strong> planar fluorophores with high symmetry, 435<br />

biochemical, 15–16<br />

blinking <strong>of</strong>, 815<br />

brightness, 817–819<br />

chemical sensing probes, 78–79<br />

colloid interactions, 846–848<br />

concentration, 805–806<br />

DNA probes, 15, 75–78<br />

dual color, 824–826<br />

excitation <strong>of</strong> multiple, 618<br />

excitation photoselection <strong>of</strong>, 357–358<br />

extrinsic, 15, 67–74<br />

membrane potential probes, 72–74<br />

membrane probes, 72<br />

photostability, 70–71<br />

protein labeling, role <strong>of</strong> Stokes shift in, 69–70<br />

protein-labeling probes, non-covalent, 71–72<br />

protein-labeling reagents, 67–69<br />

fluorescent proteins, 81–86<br />

green fluorescent protein, 81–83<br />

phycobiliproteins, 84–86<br />

phyt<strong>of</strong>luors, 83–84<br />

fluorescence-lifetime imaging microscopy, 744<br />

glucose-sensitive, 650–651<br />

intercalated, 432–433<br />

intracellular proteins<br />

specific labeling <strong>of</strong>, 86<br />

intrinsic or natural, 15, 63–67<br />

enzyme c<strong>of</strong>actors, 63–65<br />

protein binding <strong>of</strong> NADH, 65–67<br />

lanthanides, 679–683<br />

fingerprint detection, 683<br />

nanoparticles, 682<br />

near-infrared emitting, 682, 683<br />

resonance energy transfer, 680–681<br />

sensors, 681–682<br />

long-lifetime metal–ligand complexes, 683–695<br />

long-lifetime probes, 86–88<br />

lanthanides, 87–88<br />

transition metal–ligand complexes, 88<br />

long-wavelength long-lifetime, 695–697<br />

mixtures, quenching-resolved emission spectra, 301–302<br />

multiphoton excitation for membrane-bound, 613<br />

photobleaching, 769<br />

photostability, 769–770, 849–850<br />

polarization, surface-bound, 786–787<br />

polarization <strong>of</strong> single immobilized, 786<br />

probe–probe interactions, 225–226<br />

proteins as sensors, 88–89<br />

quenchers <strong>of</strong>, 278, 279<br />

red and near-IR dyes, 74–75<br />

semiconductor nanoparticles, 675–678<br />

quantum dots, labeling cells with, 677–678<br />

quantum dots, resonance energy transfer, 678<br />

quantum dots, spectral properties, 676–677<br />

single-molecule detection, 23<br />

solvent effects on emission spectra, 226–228<br />

special probes<br />

fluorogenic, 79–80<br />

structural analogs <strong>of</strong> biomolecules, 80<br />

viscosity probes, 80–81<br />

two-photon excitation <strong>of</strong>, 610–612<br />

4-Fluorotryptophan (4FW), 565<br />

FluoSphereJ, 635–636<br />

Fluro-3, 645<br />

FMN, enzyme turnover, 781–782<br />

Focused-ion-beam (FIB), 778<br />

Folate receptor, 375–376<br />

Förster, Theodor, 448<br />

Förster cycle, 261–262<br />

Förster distance (R 0 ), 14, 19, 332–333, 366, 468<br />

anisotropy decay, time-dependent, 389<br />

distance distribution from steady-state, 499, 500<br />

donor–acceptor pairs, 443–444, 468<br />

homotransfer, 450<br />

indole acceptor pair, 500<br />

proteins, 540<br />

representative, 467–468<br />

RET in three dimensions, 511<br />

Fractal dimensions, 514<br />

Fractional accessibility, 288–290, 290–291, 549<br />

Fractional intensity, 413<br />

Franck-Condon principle, 5, 8, 12, 211<br />

Franck-Condon state, 237<br />

Frequency-domain decays<br />

anisotropy, time-dependent, 383–387, 390<br />

Frequency-domain films, wide-field, 746–747

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