Oi Jiro, Terashima Tomoya, Kojima Hideto, Fujimiya Mineko, Maeda Kengo, Arai Ryohachi, Chan Lawrence, Yasuda Hitoshi, Kashiwagi Atsunori, Kimura Hiroshi
Department of Medicine, Shiga University of Medical Science, Otsu, Shiga 520-2192, Japan.
Neurosci Lett. 2008 Apr 4;434(3):266-72. doi: 10.1016/j.neulet.2008.01.062. Epub 2008 Feb 3.
We isolated peptides that home to mouse dorsal root ganglion (DRG) from a phage library expressing random 7-mer peptides fused to a minor coat protein (pIII) of the M13 phage. An in vitro biopanning procedure yielded 113 phage plaques after five cycles of enrichment by incubation with isolated DRG neurons and two cycles of subtraction by exposure to irrelevant cell lines. Analyses of the sequences of this collection identified three peptide clones that occurred repeatedly during the biopanning procedure. Phage-antibody staining revealed that the three peptides bound to DRG neurons of different sizes. To determine if the peptides would recognize neuronal cells in vivo, we injected individual GST-peptide-fusion proteins into the subarachnoid space of mice and observed the appearance of immunoreactive GST in the cytosol of DRG neurons with a similar size distribution as that observed in vitro, indicating that the GST-peptide-fusion proteins were recognized and taken up by different DRG neurons in vivo. The identification of homing peptide sequences provides a powerful tool for future studies on DRG neuronal function in vitro and in vivo, and opens up the possibility of neuron-specific drug and gene delivery in the treatment of diseases affecting DRG neurons.
我们从一个噬菌体文库中分离出靶向小鼠背根神经节(DRG)的肽段,该文库表达与M13噬菌体的次要外壳蛋白(pIII)融合的随机7肽。通过体外生物淘选程序,在与分离的DRG神经元孵育进行五个富集循环以及与无关细胞系接触进行两个减除循环后,获得了113个噬菌斑。对该集合的序列分析确定了在生物淘选过程中反复出现的三个肽克隆。噬菌体 - 抗体染色显示这三种肽与不同大小的DRG神经元结合。为了确定这些肽在体内是否能识别神经元细胞,我们将单个GST - 肽融合蛋白注射到小鼠蛛网膜下腔,并观察到DRG神经元胞质溶胶中出现免疫反应性GST,其大小分布与体外观察到的相似,这表明GST - 肽融合蛋白在体内被不同的DRG神经元识别并摄取。归巢肽序列的鉴定为未来体外和体内DRG神经元功能研究提供了强大工具,并为治疗影响DRG神经元的疾病时进行神经元特异性药物和基因递送开辟了可能性。