Synthesis of steroid tracers with a oxyme ligation method and use thereof in fluorescent polarisation immunoassay

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A method for the synthesis of ketosteroid oxime conjugates with a fluorescein (6-FAM) derivative connected via a short bifunctional aminooxypropyl linker is proposed. The conjugates were used as tracers for fluorescence polarization immunoassay (FPIA) with monoclonal antibodies. Stereoisomers by the oxime group were separated by preparative RP TLC and HPLC and tested in the FPIA method. Binding parameters of of tracers with monoclonal antibodies (mAbs) to progesterone were studied. Tracers showed high efficiency in the analysis of steroid hormones, the detection limit of progesterone being lower than that for a previously described analog. The Z-isomer was found to be more sensitive in the FPIA analysis compared to the E-isomer.

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作者简介

I. Prokhorenko

Shemyakin–Ovchinnikov Institute of Bioorganic Chemistry RAS

编辑信件的主要联系方式.
Email: prig67@mail.ru
俄罗斯联邦, ul. Miklukho-Maklaya 16/10, Moscow, 117997

D. Glushchenko

Shemyakin–Ovchinnikov Institute of Bioorganic Chemistry RAS

Email: prig67@mail.ru
俄罗斯联邦, ul. Miklukho-Maklaya 16/10, Moscow, 117997

E. Gulyak

Shemyakin–Ovchinnikov Institute of Bioorganic Chemistry RAS

Email: prig67@mail.ru
俄罗斯联邦, ul. Miklukho-Maklaya 16/10, Moscow, 117997

I. Mikhura

Shemyakin–Ovchinnikov Institute of Bioorganic Chemistry RAS

Email: prig67@mail.ru
俄罗斯联邦, ul. Miklukho-Maklaya 16/10, Moscow, 117997

V. Korshun

Shemyakin–Ovchinnikov Institute of Bioorganic Chemistry RAS

Email: prig67@mail.ru
俄罗斯联邦, ul. Miklukho-Maklaya 16/10, Moscow, 117997

L. Mukhametova

Lomonosov Moscow State University

Email: prig67@mail.ru

Department of Chemistry

俄罗斯联邦, Leninskiye Gory 1/3, Moscow, 119991

S. Eremin

Lomonosov Moscow State University

Email: prig67@mail.ru

Department of Chemistry

俄罗斯联邦, Leninskiye Gory 1/3, Moscow, 119991

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补充文件

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1. JATS XML
2. Fig. 1. Structure of previously described tracers for FPIA based on steroid hormones: (a) – Pg3CMO-EDF (progesterone carboxymethyloxime amide with ethylenediamine fluorescein thiocarbamate); (b) – 11-α-hydroxyprogesterone, acylated with succinic anhydride.

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3. Fig. 2. Stereoisomeric fragments of oximes (VII) and (VIII).

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4. Fig. 3. Change in the fluorescence polarization signal of free tracers E(VII), Z(VII) and Pg3CMO-EDF (2.5 nM) during the formation of complexes with specific antibodies to progesterone MAb-Pg (20 nM) in comparison with nonspecific MAb-3G11 (30 nM ).

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5. Fig. 4. Dependence of changes in the fluorescence polarization signal on the concentration of antibodies for tracers E(VII) (curve 1), Z(VII) (curve 2) and Pg3CMO-EDF (curve 3) (tracer concentration 2.5 nM); pH 8.5, 25°C.

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6. Fig. 5. Calibration dependences (a) and normalized calibration dependences (b) for tracers E(VII) (curve 1), Z(VII) (curve 2) and Pg3CMO-EDF (curve 3) (tracer concentrations 2.5 nM); pH 8.5, 25°C.

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7. Scheme 1. Synthesis of bifunctional linker reagent (V).

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8. Scheme 2. Synthesis of the ethoxyethylidene-protected aminooxy derivative (VI) of 6-carboxyfluorescein (6-FAM) and fluorescent tracers (VII) and (VIII).

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