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基于 HPMA 共聚物的生物相容糖基纳米材料,用于半乳糖凝集素-3 的特异性靶向。

Biocompatible glyconanomaterials based on HPMA-copolymer for specific targeting of galectin-3.

机构信息

Institute of Microbiology, Czech Academy of Sciences, Vídeňská 1083, 14220, Prague 4, Czech Republic.

Institute of Macromolecular Chemistry, Czech Academy of Sciences, Heyrovský Sq. 2, 16206, Prague 6, Czech Republic.

出版信息

J Nanobiotechnology. 2018 Sep 20;16(1):73. doi: 10.1186/s12951-018-0399-1.

Abstract

BACKGROUND

Galectin-3 (Gal-3) is a promising target in cancer therapy with a high therapeutic potential due to its abundant localization within the tumor tissue and its involvement in tumor development and proliferation. Potential clinical application of Gal-3-targeted inhibitors is often complicated by their insufficient selectivity or low biocompatibility. Nanomaterials based on N-(2-hydroxypropyl)methacrylamide (HPMA) nanocarrier are attractive for in vivo application due to their good water solubility and lack of toxicity and immunogenicity. Their conjugation with tailored carbohydrate ligands can yield specific glyconanomaterials applicable for targeting biomedicinally relevant lectins like Gal-3.

RESULTS

In the present study we describe the synthesis and the structure-affinity relationship study of novel Gal-3-targeted glyconanomaterials, based on hydrophilic HPMA nanocarriers. HPMA nanocarriers decorated with varying amounts of Gal-3 specific epitope GalNAcβ1,4GlcNAc (LacdiNAc) were analyzed in a competitive ELISA-type assay and their binding kinetics was described by surface plasmon resonance. We showed the impact of various linker types and epitope distribution on the binding affinity to Gal-3. The synthesis of specific functionalized LacdiNAc epitopes was accomplished under the catalysis by mutant β-N-acetylhexosaminidases. The glycans were conjugated to statistic HPMA copolymer precursors through diverse linkers in a defined pattern and density using Cu(I)-catalyzed azide-alkyne cycloaddition. The resulting water-soluble and structurally flexible synthetic glyconanomaterials exhibited affinity to Gal-3 in low μM range.

CONCLUSIONS

The results of this study reveal the relation between the linker structure, glycan distribution and the affinity of the glycopolymer nanomaterial to Gal-3. They pave the way to specific biomedicinal glyconanomaterials that target Gal-3 as a therapeutic goal in cancerogenesis and other disorders.

摘要

背景

半乳糖凝集素-3(Gal-3)是癌症治疗中很有前途的靶点,因为它在肿瘤组织中丰富的定位及其参与肿瘤的发展和增殖。Gal-3 靶向抑制剂的潜在临床应用常常受到其选择性不足或生物相容性低的限制。基于 N-(2-羟丙基)甲基丙烯酰胺(HPMA)纳米载体的纳米材料由于其良好的水溶性、缺乏毒性和免疫原性,对于体内应用具有吸引力。它们与定制的碳水化合物配体的缀合可以产生特定的糖纳米材料,适用于靶向与生物医学相关的凝集素,如 Gal-3。

结果

在本研究中,我们描述了基于亲水性 HPMA 纳米载体的新型 Gal-3 靶向糖纳米材料的合成和结构亲和力关系研究。用不同数量的 Gal-3 特异性表位半乳糖-N-乙酰氨基半乳糖(GalNAcβ1,4GlcNAc,LacdiNAc)修饰的 HPMA 纳米载体在竞争性 ELISA 型测定中进行了分析,并通过表面等离子体共振描述了它们的结合动力学。我们展示了不同连接体类型和表位分布对与 Gal-3 结合亲和力的影响。在突变的β-N-乙酰氨基己糖苷酶的催化下,完成了特定功能化 LacdiNAc 表位的合成。通过铜(I)催化的叠氮-炔环加成反应,以定义的模式和密度,将糖苷通过各种连接体连接到统计 HPMA 共聚物前体上。所得的水溶性和结构灵活的合成糖纳米材料在低μM 范围内对 Gal-3 具有亲和力。

结论

这项研究的结果揭示了连接体结构、糖分布与糖聚合物纳米材料与 Gal-3 亲和力之间的关系。它们为靶向 Gal-3 作为癌症发生和其他疾病的治疗目标的特定生物医学糖纳米材料铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fb7/6146777/e01a1269875f/12951_2018_399_Sch1_HTML.jpg

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