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用光敏脂质体纳米载体对 Siglecs 进行定制化多价靶向。

Tailored Multivalent Targeting of Siglecs with Photosensitizing Liposome Nanocarriers.

机构信息

Department of Organic Chemistry, Universidad Autónoma de Madrid, Campus de Cantoblanco, 28049, Madrid, Spain.

Department of Molecules & Materials, MESA+ Institute for Nanotechnology, Faculty of Science and Technology, University of Twente, P.O. Box 217, 7500 AE, Enschede, The Netherlands.

出版信息

Angew Chem Int Ed Engl. 2022 Aug 1;61(31):e202206900. doi: 10.1002/anie.202206900. Epub 2022 Jun 21.

Abstract

The modification of surfaces with multiple ligands allows the formation of platforms for the study of multivalency in diverse processes. Herein we use this approach for the implementation of a photosensitizer (PS)-nanocarrier system that binds efficiently to siglec-10, a member of the CD33 family of siglecs (sialic acid (SA)-binding immunoglobulin-like lectins). In particular, a zinc phthalocyanine derivative bearing three SA moieties (PcSA) has been incorporated in the membrane of small unilamellar vesicles (SUVs), retaining its photophysical properties upon insertion into the SUV's membrane. The interaction of these biohybrid systems with human siglec-10-displaying supported lipid bilayers (SLBs) has shown the occurrence of weakly multivalent, superselective interactions between vesicle and SLB. The SLB therefore acts as an excellent cell membrane mimic, while the binding with PS-loaded SUVs shows the potential for targeting siglec-expressing cells with photosensitizing nanocarriers.

摘要

通过表面的多重配体修饰,可以形成用于研究多种过程中多价相互作用的平台。在此,我们采用这种方法构建了一种光敏剂(PS)-纳米载体系统,该系统能够有效地与 Siglec-10 结合,Siglec-10 是 Siglec 家族(唾液酸(SA)结合免疫球蛋白样凝集素)的成员之一。具体来说,带有三个 SA 部分的锌酞菁衍生物(PcSA)已被掺入到小单层囊泡(SUV)的膜中,在插入 SUV 膜后保留其光物理性质。这些生物杂化系统与展示人 Siglec-10 的支持脂质双层(SLB)的相互作用表明,囊泡和 SLB 之间发生了弱多价、超选择性相互作用。因此,SLB 可以作为出色的细胞膜模拟物,而与负载 PS 的 SUV 的结合则显示出使用光敏纳米载体靶向表达 Siglec 的细胞的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b83/9401027/121ef6a08ac0/ANIE-61-0-g006.jpg

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