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多价相互作用:促黑素多聚体的合成与评估——黑色素瘤靶向工具

Multivalent Interactions: Synthesis and Evaluation of Melanotropin Multimers - Tools for Melanoma Targeting.

作者信息

Brabez Nabila, Saunders Kara, Nguyen Kevin L, Jayasundera Thanuja B M, Weber Craig, Lynch Ronald M, Chassaing Gerard, Lavielle Solange, Hruby Victor J

机构信息

UPMC Paris 06, UMR 7203, Laboratoire des BioMolécules, Université P. et M. Curie, 75005 Paris France ; CNRS, UMR 7203, France ; ENS, UMR 7203, Département de Chimie, Ecole Normale Supérieure, 75005 Paris France ; University of Arizona, Department of Chemistry and Biochemistry, Tucson, AZ 85721, USA.

出版信息

ACS Med Chem Lett. 2013 Jan 1;4(1):98-102. doi: 10.1021/ml300312b. Epub 2012 Nov 24.

Abstract

In order to develop agents for early detection and selective treatment of melanomas, high affinity and high specificity molecular tools are required. Enhanced specificity may be obtained by simultaneously binding to multiple cell surface targets the use of multimeric analogs of naturally occurring ligands. Trimers targeting overexpressed melanocortin receptors have been found to be potential candidates for this purpose. In the present letter, we describe the synthesis and study of multimers based on a dendrimer-like scaffold. The binding affinity and activity results revealed that dendrimers promote multivalent interactions via statistical and/or cooperative effects on binding. Moreover, viability studies showed no significant toxicity at micromolar concentrations, which will allow these molecular complexes to be used . Finally, imaging studies showed effective internalization for all the molecules confirming their potential as delivery agents.

摘要

为了开发用于黑色素瘤早期检测和选择性治疗的药物,需要高亲和力和高特异性的分子工具。通过同时结合多个细胞表面靶点(使用天然存在的配体的多聚体类似物)可以提高特异性。已发现靶向过表达的黑皮质素受体的三聚体是实现这一目的的潜在候选物。在本信函中,我们描述了基于树枝状支架的多聚体的合成与研究。结合亲和力和活性结果表明,树枝状大分子通过对结合的统计和/或协同效应促进多价相互作用。此外,活力研究表明在微摩尔浓度下无明显毒性,这将使这些分子复合物得以应用。最后,成像研究表明所有分子都能有效内化,证实了它们作为递送剂的潜力。

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