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Time-Resolved Tryptophan Fluorescence as an Indicator of Alterations in Serum Proteins in Melancholic Depression

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Abstract—The goal of this work was to search for blood serum parameters that would be associated with the state of patients with mental disorders. Such indicators are needed for an objective assessment of this state versus the prevailing subjective evaluation methodologies. The kinetics of tryptophan fluorescence decay in the serum albumin fraction was compared in patients with melancholic depression (before treatment) and in healthy volunteers. Albumin fluorescence is mainly due to the tryptophan 214 residue, which is located in the immediate vicinity of the first drug-binding center of the molecule. The decay kinetics were described as a sum of three exponential functions with lifetimes τi (in the 6.5, 2.8 and 1.0 ns region) and the amplitudes Ai. The τi values were similar in both groups of individuals. In contrast, there was a significant difference between patients and controls in the A1/A3 amplitude ratio. It is suggested that the A1/A3 value can be considered as a potential marker indicating the presence or absence of melancholic depression in patients before treatment.

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COMPLIANCE WITH ETHICAL STANDARDS

Conflict of interests. The authors declare that they have no conflict of interest.

Statement of compliance with standards of research involving humans as subjects. All subjects gave their informed consent to participation in the study. The study was conducted in agreement with the Helsinki Declaration on the Ethical Principles of Medical Research in Human Subjects and the conclusion of the Ethics Committee of the Moscow Research Institute of Psychiatry (protocol no. 16 from March 13, 2017).

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Correspondence to N. V. Smolina.

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Translated by D. Timchenko

Abbreviation: HSA, human serum albumin.

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Syrejshchikova, T.I., Smolina, N.V., Brilliantova, V.V. et al. Time-Resolved Tryptophan Fluorescence as an Indicator of Alterations in Serum Proteins in Melancholic Depression. BIOPHYSICS 64, 95–99 (2019). https://doi.org/10.1134/S0006350919010184

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  • DOI: https://doi.org/10.1134/S0006350919010184

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