Literature DB >> 16113120

Pulsed interleaved excitation.

Barbara K Müller1, Evgeny Zaychikov, Christoph Bräuchle, Don C Lamb.   

Abstract

In this article, we demonstrate the new method of pulsed interleaved excitation (PIE), which can be used to extend the capabilities of multiple-color fluorescence imaging, fluorescence cross-correlation spectroscopy (FCCS), and single-pair fluorescence resonance energy transfer (spFRET) measurements. In PIE, multiple excitation sources are interleaved such that the fluorescence emission generated from one pulse is complete before the next excitation pulse arrives. Hence, the excitation source for each detected photon is known. Typical repetition rates used for PIE are between approximately 1 and 50 MHz. PIE has many applications in various fluorescence methods. Using PIE, dual-color measurements can be performed with a single detector. In fluorescence imaging with multicolor detection, spectral cross talk can be removed, improving the contrast of the image. Using PIE with FCCS, we can eliminate spectral cross talk, making the method sensitive to weaker interactions. FCCS measurements with complexes that undergo FRET can be analyzed quantitatively. Under specific conditions, the FRET efficiency can be determined directly from the amplitude of the measured correlation functions without any calibration factors. We also show the application of PIE to spFRET measurements, where complexes that have low FRET efficiency can be distinguished from those that do not have an active acceptor.

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Year:  2005        PMID: 16113120      PMCID: PMC1366845          DOI: 10.1529/biophysj.105.064766

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  36 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-30       Impact factor: 11.205

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5.  Cross talk free fluorescence cross correlation spectroscopy in live cells.

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6.  Single-molecule measurement of protein folding kinetics.

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7.  Triplet-state monitoring by fluorescence correlation spectroscopy.

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Journal:  J Fluoresc       Date:  1994-09       Impact factor: 2.217

8.  Monitoring conformational dynamics of a single molecule by selective fluorescence spectroscopy.

Authors:  C Eggeling; J R Fries; L Brand; R Günther; C A Seidel
Journal:  Proc Natl Acad Sci U S A       Date:  1998-02-17       Impact factor: 11.205

9.  Fluorescence correlation spectroscopy. II. An experimental realization.

Authors:  D Magde; E L Elson; W W Webb
Journal:  Biopolymers       Date:  1974-01       Impact factor: 2.505

10.  Purification of polyethylenimine polyplexes highlights the role of free polycations in gene transfer.

Authors:  Sabine Boeckle; Katharina von Gersdorff; Silke van der Piepen; Carsten Culmsee; Ernst Wagner; Manfred Ogris
Journal:  J Gene Med       Date:  2004-10       Impact factor: 4.565

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  149 in total

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4.  Single-molecule tools elucidate H2A.Z nucleosome composition.

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5.  Effects of Hofmeister ions on the α-helical structure of proteins.

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6.  Disentangling subpopulations in single-molecule FRET and ALEX experiments with photon distribution analysis.

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Journal:  Biophys J       Date:  2012-03-06       Impact factor: 4.033

7.  Factors affecting the quantification of biomolecular interactions by fluorescence cross-correlation spectroscopy.

Authors:  Yong Hwee Foo; Nikolaus Naredi-Rainer; Don C Lamb; Sohail Ahmed; Thorsten Wohland
Journal:  Biophys J       Date:  2012-03-06       Impact factor: 4.033

8.  Relaxation Kinetics by Fluorescence Correlation Spectroscopy: Determination of Kinetic Parameters in the Presence of Fluorescent Impurities.

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Journal:  J Phys Chem Lett       Date:  2010-04-09       Impact factor: 6.475

9.  Single-molecule spectroscopy of protein folding in a chaperonin cage.

Authors:  Hagen Hofmann; Frank Hillger; Shawn H Pfeil; Armin Hoffmann; Daniel Streich; Dominik Haenni; Daniel Nettels; Everett A Lipman; Benjamin Schuler
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10.  Substrate discrimination of the chaperone BiP by autonomous and cochaperone-regulated conformational transitions.

Authors:  Moritz Marcinowski; Matthias Höller; Matthias J Feige; Danae Baerend; Don C Lamb; Johannes Buchner
Journal:  Nat Struct Mol Biol       Date:  2011-01-09       Impact factor: 15.369

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