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Clickable Methyltetrazine-lndocarbocyanine Lipids: A Multicolor Tool Kit for Efficient Modifications of Cell Membranes

机译:可点击的甲基四苯胺 - 氯萘碳菁脂质:一种用于有效修饰细胞膜的多色工具试剂盒

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摘要

Cell-based therapeutics are one of the most promising and exciting breakthroughs in modern medicine. Modification of the cell surface with ligands, biologics, drugs, and nanoparticles can further enhance the functionality. Previously, we described the synthesis of a dioctadecyl indocarbocyanine Cy3 analog (aminomethyl-DiI) for efficient and stable modification (painting) of mouse erythrocytes with small molecules, enzymes, and biologics. Here, we synthesized a near-infrared aminomethyl dioctadecyl derivative of Cy7 (aminomethyl-DOCy7) and systematically compared it to aminomethyl-DiI as an anchor for the modification of human erythrocytes, Jurkat cells, and primary T cells with immunoglobulin G. To enable copper-free click chemistry modification of cell membranes, we conjugated a methyltetrazine (MTz) group to the amino-indocyanine lipids via a polyethylene glycol (PEG) linker. DOCy7-PEG3400-MTz showed over 99% modification efficiency of human red blood cells (RBCs) at 25 mu M. Reaction of trans-cyclooctene (TCO) modified immunoglobulin G (IgG) with DOCy7-PEG(4)-MTz-modified RBCs (2-step method) resulted in similar to 80,000 IgG molecules per erythrocyte, whereas modification with a preconjugated DOCy7-PEG3400-IgG construct (1-step method) resulted in similar to 20,000 IgG molecules per erythrocyte as detected by immuno dot-blot. The number of IgG/RBC was controlled by the concentration of IgG. The incubation of RBCs with DiI-PEG3400-MTz resulted in a similar number of IgG/RBC. Modification of the T-lymphocyte cell line Jurkat with IgG resulted in similar to 1 x 10(6) IgG/cell with the 1-step and 2-step methods, and the efficiency was similar for DOCy7 and DiI constructs. Finally, we used DOCy7 and DiI constructs to demonstrate efficient modification of primary CD3+T cells from healthy donors. In conclusion, click indocarbocyanine conjugates represent a novel multicolor chemical biology tool kit for efficient surface modification of different cells types and can be used for potential imaging and drug delivery applications involving engineered cells.
机译:基于细胞的治疗方法是现代医学中最有前途和最令人兴奋的突破之一。用配体,生物学,药物和纳米颗粒改性细胞表面可以进一步增强功能。以前,我们描述了用小分子,酶和生物学的小鼠红细胞的高效稳定改性(涂料)的二辛酰吲哚碳菁Cy3(氨基甲基-III)的合成。在此,我们合成Cy7(氨基甲基-Cocy7)的近红外氨基甲基二甲基二烯基衍生物,并系统地将其与氨基甲基-III相比作为用于改性人的红细胞,Jurkat细胞和用免疫球蛋白G的初级T细胞的锚。实现铜 - 用聚乙二醇(PEG)接头将甲基四氮(MTZ)基团与氨基 - 吲哚菁脂质缀合的化学改性。 Docy7-PEG3400-MTZ在25μmMMMMMM中显示出超过99%的人红细胞(RBC)的改性效率(RBCS)。反式环辛烯(TCO)改性免疫球蛋白G(IgG)与Docy7-PEG(4)-MTZ改性的RBCs的反应(2步方法)导致每种红细胞的80,000个IgG分子相似,而用预缀合的Docy7-PEG3400-IgG构建体(1步法)改性导致每种红细胞的20,000 IgG分子相似,如通过免疫点印检测到的每种红细胞。 IgG / RBC的数量由IgG的浓度控制。用DII-PEG3400-MTZ孵育RBCS导致类似数量的IgG / RBC。用IgG的改性T淋巴细胞细胞系Jurkat导致与1×10(6)个IgG /电池相似,具有1步和2步方法,对于Docy7和DII构建体的效率类似。最后,我们使用Docy7和DII构建体来证明来自健康供体的主要CD3 + T细胞的有效修饰。总之,点击室内氰基缀合物代表新型多色化学生物学工具试剂盒,用于有效的不同细胞类型的表面改性,可用于涉及工程细胞的潜在成像和药物递送应用。

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  • 来源
    《Bioconjugate Chemistry》 |2019年第8期|共9页
  • 作者单位

    Univ Colorado Skaggs Sch Pharm &

    Pharmaceut Sci Translat Bionanosci Lab Anschutz Med Campus Aurora CO 80045 USA;

    Univ Colorado Skaggs Sch Pharm &

    Pharmaceut Sci Translat Bionanosci Lab Anschutz Med Campus Aurora CO 80045 USA;

    Univ Colorado Skaggs Sch Pharm &

    Pharmaceut Sci Translat Bionanosci Lab Anschutz Med Campus Aurora CO 80045 USA;

    Univ Colorado Denver Dept Biochem &

    Mol Genet Anschutz Med Campus Aurora CO 80045 USA;

    Univ Colorado Denver Dept Biochem &

    Mol Genet Anschutz Med Campus Aurora CO 80045 USA;

    Univ Colorado Sch Med Div Hematol Anschutz Med Campus Aurora CO 80045 USA;

    Univ Colorado Sch Med Div Hematol Anschutz Med Campus Aurora CO 80045 USA;

    Univ Colorado Skaggs Sch Pharm &

    Pharmaceut Sci Translat Bionanosci Lab Anschutz Med Campus Aurora CO 80045 USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物化学;
  • 关键词

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