Using polarized Total Synchronous Fluorescence Spectroscopy (pTSFS) with PARAFAC analysis for characterizing intrinsic protein emission
Steiner-Browne, Marina Elcoroaristizabal, Saioa Ryder, Alan G.
Steiner-Browne, Marina
Elcoroaristizabal, Saioa
Ryder, Alan G.
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Publication Date
2019-10-15
Type
Article
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Steiner-Browne, Marina, Elcoroaristizabal, Saioa, & Ryder, Alan G. (2019). Using polarized Total Synchronous Fluorescence Spectroscopy (pTSFS) with PARAFAC analysis for characterizing intrinsic protein emission. Chemometrics and Intelligent Laboratory Systems, 194, 103871. doi: 10.1016/j.chemolab.2019.103871
Abstract
Using polarized Excitation Emission Matrix (pEEM) spectroscopy to measure the intrinsic emission of proteins offers a potentially useful methodology for a wide variety of potential applications. However, the presence of Rayleigh light scatter causes significant problems when attempting to use Parallel Factor (PARAFAC) and for anisotropy calculations. The use of polarized Total Synchronous Fluorescence Spectroscopy (pTSFS) can minimize Rayleigh scatter and avoid the use of complex data correction methods. Here, we investigated for the first time the use of pTSFS and PARAFAC to analyze the intrinsic emission of an Immunoglobulin (IgG) type protein in its native state. To enable PARAFAC analysis however, TSFS data (which is not trilinear) must first be transformed into an EEM like layout (t-EEM) and this generated a region with no experimentally acquired information (92% of the explained variance, and a much weaker, mostly Tyr related emission with ~3% of the explained variance. The recovery of this Tyr component was only possible because pTSFS measurements were less contaminated by Rayleigh scattering. Changes in Tyr-to-Trp energy transfer rates caused by thermal motion were detected as an increase in Tyr contribution, which could not be resolved with the equivalent pEEM measurements due to light scatter contamination. The increased selectivity, sensitivity, and reproducibility of pTSFS measurements shows that this is a better option than pEEM for fluorescence emission based monitoring of protein structural change or lot-to-lot variance of IgG type proteins.
Publisher
Elsevier
Publisher DOI
10.1016/j.chemolab.2019.103871
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Attribution-NonCommercial-NoDerivs 3.0 Ireland