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Measuring enzyme binding using shaped ultrafast laser pulses

  • Dickinson College, Pennsylvania
  • Stony Brook University

Research output: Chapter in Book/Report/Conference proceedingConference contributionpeer-review

Abstract

We use multiphoton quantum-control spectroscopy to discriminate between enzyme-bound and unbound NADH (reduced nicotinamide adenine dinucleotide) molecules in solution. Shaped ultrafast laser pulses are used to illuminate both forms of NADH, and the ratio of the fluorescence from the bound and unbound molecules for different pulse shapes allows us to measure binding without spectrally resolving the emitted fluorescence or relying on the absolute fluorescence yield. This permits determination of enzyme binding in situations where spectrally resolved measurements and absolute fluorescence yields are difficult to obtain, and makes the approach ideal for multiphoton microscopy with molecular discrimination.

Original languageEnglish
Title of host publication18th International Conference on Ultrafast Phenomena, UP 2012
DOIs
StatePublished - 2013
Event18th International Conference on Ultrafast Phenomena, UP 2012 - Lausanne, Switzerland
Duration: Jul 8 2012Jul 13 2012

Publication series

NameEPJ Web of Conferences
Volume41
ISSN (Print)2101-6275
ISSN (Electronic)2100-014X

Conference

Conference18th International Conference on Ultrafast Phenomena, UP 2012
Country/TerritorySwitzerland
CityLausanne
Period07/8/1207/13/12

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