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Development of Cyclic NGR Peptides with Thioether Linkage:Structure and Dynamics Determining Deamidation and Bioactivity

Enyedi, Kata N. and Czajlik, András and Knapp, Krisztina and Láng, András and Majer, Zsuzsa and Lajkó, Eszter and Kőhidai, László and Perczel, András and Mező, Gábor (2015) Development of Cyclic NGR Peptides with Thioether Linkage:Structure and Dynamics Determining Deamidation and Bioactivity. Journal of Medicinal Chemistry, 589. pp. 1806-1817. ISSN 0022-2623

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Abstract

NGR peptides that recognize CD13 receptors in tumor neovasculature are of high interest, in particular due to their potential applications in drug targeting. Here we report the synthesis and structural analysis of novel thioether bond-linked cyclic NGR peptides. Our results show that their chemostability (resistance against spontaneous decomposition forming isoAsp and Asp derivatives) strongly depends on both sample handling conditions and structural properties. A significant correlation was found between chemostability and structural measures, such as NHGly−COAsn‑sc distances. The sidechain orientation of Asn is a key determining factor; if it is turned away from HNGly, the chemostability increases. Structure stabilizing factors (e.g., H-bonds) lower their internal dynamics, and thus biomolecules become even more resistant against spontaneous decomposition. The effect of cyclic NGR peptides on cell adhesion was examined in A2058 melanoma cell lines. It was found that some of the investigated peptides gradually increased cell adhesion with long-term characteristics, indicating time-dependent formation of integrin binding isoAsp derivatives that are responsible for the adhesion-inducing effect.

Item Type: Article
Subjects: Q Science / természettudomány > QD Chemistry / kémia > QD04 Organic chemistry / szerves kémia
R Medicine / orvostudomány > RM Therapeutics. Pharmacology / terápia, gyógyszertan
Depositing User: Dr Katalin Uray
Date Deposited: 13 Jan 2016 11:18
Last Modified: 03 Feb 2016 00:15
URI: http://real.mtak.hu/id/eprint/31715

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