Myelopeptide MP-5 and fluorescent derivatives: Synthesis and biological activity

The Val-Val-Tyr-Pro-Asp bone marrow peptide (MP-5) and its analogue (MP-5-Lys) were synthesized. Fluorescent derivatives, Ftc-MP-5 and MP-5-Lys(Ftc), were prepared. The iological activity of MP-5 and MP-5-Lys was studied in vitro and in vivo. The MP-5 peptide caused 60–84% inhibition of growth of th...

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Veröffentlicht in:Russian journal of bioorganic chemistry 2008-07, Vol.34 (4), p.404-408
Hauptverfasser: Fonina, L. A., Az’muko, A. A., Kalikhevich, V. N., Lewit, M. L., Ardemasova, Z. A., Gur’yanov, S. A., Belevskaya, R. G., Efremov, M. A., Treshchalina, E. M., Mikhailova, A. A.
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container_end_page 408
container_issue 4
container_start_page 404
container_title Russian journal of bioorganic chemistry
container_volume 34
creator Fonina, L. A.
Az’muko, A. A.
Kalikhevich, V. N.
Lewit, M. L.
Ardemasova, Z. A.
Gur’yanov, S. A.
Belevskaya, R. G.
Efremov, M. A.
Treshchalina, E. M.
Mikhailova, A. A.
description The Val-Val-Tyr-Pro-Asp bone marrow peptide (MP-5) and its analogue (MP-5-Lys) were synthesized. Fluorescent derivatives, Ftc-MP-5 and MP-5-Lys(Ftc), were prepared. The iological activity of MP-5 and MP-5-Lys was studied in vitro and in vivo. The MP-5 peptide caused 60–84% inhibition of growth of the following mouse cancers: lymphatic leukemia P388, melanoma B-16, and cervical carcinoma CUC-5. These peptides also restored functional activity of T-lymphocytes that was inhibited by metabolic products of the HL-60 leukemic cell line. MP-5-Lys(Ftc) was shown to preserve the functional properties of MP-5 towards T-lymphocytes, but Ftc-MP-5 was practically inactive.
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subjects Biochemistry
Biomedical and Life Sciences
Biomedicine
Bioorganic Chemistry
Life Sciences
Organic Chemistry
Review Articles
title Myelopeptide MP-5 and fluorescent derivatives: Synthesis and biological activity
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