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Micro-Volume Couette Flow Sample Orientation for Absorbance and Fluorescence Linear Dichroism

Rachel Marrington ^*, Timothy R. Dafforn , David J. Halsall  and Alison Rodger ^*

^* Department of Chemistry, University of Warwick, Coventry, CV4 7AL, United Kingdom; Biosciences, University of Birmingham, Edgbaston, Birmingham, B15 2TT, United Kingdom; and Department of Clinical Biochemistry, Addenbrooke's Hospital, Cambridge, CB2 2QQ, United Kingdom

Correspondence: Address reprint requests to Alison Rodger, E-mail: a.rodger{at}warwick.ac.uk.

Linear dichroism (LD) can be used to study the alignment of absorbing chromophores within long molecules. In particular, Couette flow LD has been used to good effect in probing ligand binding to DNA and to fibrous proteins. This technique has been previously limited by large sample requirements. Here we report the design and application of a new micro-volume Couette flow cell that significantly enhances the potential applications of flow LD spectroscopy by reducing the sample requirements for flow linear dichroism to 25 µL (with concentrations such that the absorbance maximum of the sample in a 1-cm pathlength cuvette is 1). The micro-volume Couette cell has also enabled the measurement of fluorescence-detected Couette flow linear dichroism. This new technique enables the orientation of fluorescent ligands to be probed even when their electronic transitions overlap with those of the macromolecule and conversely. The potential of flow-oriented fluorescence dichroism and application of the micro-volume Couette LD cell are illustrated by the collection of data for DNA with minor groove and intercalating ligands: DAPI, Hoechst, and ethidium bromide. As with conventional fluorescence, improved sensitivity compared with absorbance LD is to be expected after instrumentation optimization.

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