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Nanometer-Sized Aggregates Generated Using Short Solubility Controlling Peptide Tags Do Increase the In Vivo Immunogenicity of a Nonimmunogenic Protein

机译:使用短溶解度控制肽标签产生的纳米尺寸的聚集体确实增加了非免疫蛋白的体内免疫原性

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Subvisible aggregates of proteins are suspected to cause adverse immune response, and a recent FDA guideline has recommended the monitoring of micrometer-sized aggregates (2-10 mu m) though recognizing that the underlying mechanism behind aggregation and immunogenicity remains unclear. Here, we report a correlation between the immunogenicity and the size of nanometer-scaled aggregates of a small 6.5 kDa model protein, bovine pancreatic trypsin inhibitor (BPTI) variant. BPTI-19A, a monomeric and nonimmunogenic protein, was oligomerized into subvisible aggregates with hydrodynamic radii (R-h) of 3-4 nm by attaching hydrophobic solubility controlling peptide (SCP) tags to its C-terminus. The results showed that the association of nonimmunogenic BPTI into nanometer-sized subvisible aggregates made it highly immunogenic, as assessed by the IgG antibody titers of the mice's sera. Overall, the study emphasizes that subvisible aggregates, as small as a few nanometers, which are presently ignored, are worth monitoring for deciphering the origin of undesired immunogenicity of therapeutic proteins.
机译:怀疑蛋白质的可疑蛋白质含量造成不良免疫应答,最近的FDA指南推荐监测微米尺寸的聚集体(2-10μm),尽管认识到聚集背后的潜在机制和免疫原性仍不清楚。在此,我们报告了小型6.5kDa模型蛋白,牛胰胰蛋白酶抑制剂(BPTI)变体的免疫原性和纳米缩放聚集体的尺寸之间的相关性。通过将疏水溶解度控制肽(SCP)标签连接到其C-末端,BPTI-19A,单体和非免化蛋白质,用疏水性溶解度控制肽(SCP)标签将疏水性溶解度控制(SCP)标签连接到3-4nm的水动力半径(R-H)中。结果表明,非免疫性BPTI与纳米尺寸的亚可残物聚集体的结合使其具有高度免疫原性,如通过小鼠血清的IgG抗体滴度评估。总的来说,该研究强调,该潜在的聚集体,如目前忽略的几纳米,值得监测用于解密治疗蛋白的不希望的免疫原性的起源。

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