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Biological Characterization of Commercial Recombinantly Expressed Immunomodulating Proteins Contaminated with Bacterial Products in the Year 2020: The SAA3 Case

机译:2020年含有细菌产品污染的商业重组表达免疫调节蛋白的生物学特征:SAA3案例

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The serum amyloid A (SAA) gene family is highly conserved and encodes acute phase proteins that are upregulated in response to inflammatory triggers. Over the years, a considerable amount of literature has been published attributing a wide range of biological effects to SAAs such as leukocyte recruitment, cytokine and chemokine expression and induction of matrix metalloproteinases. Furthermore, SAAs have also been linked to protumorigenic, proatherogenic and anti-inflammatory effects. Here, we investigated the biological effects conveyed by murine SAA3 (mu rSAA3) recombinantly expressed in Escherichia coli. We observed the upregulation of a number of chemokines including CCL2, CCL3, CXCL1, CXCL2, CXCL6 or CXCL8 following stimulation of monocytic, fibroblastoid and peritoneal cells with mu rSAA3. Furthermore, this SAA variant displayed potent in vivo recruitment of neutrophils through the activation of TLR4. However, a major problem associated with proteins derived from recombinant expression in bacteria is potential contamination with various bacterial products, such as lipopolysaccharide, lipoproteins and formylated peptides. This is of particular relevance in the case of SAA as there currently exists a discrepancy in biological activity between SAA derived from recombinant expression and that of an endogenous source, i.e. inflammatory plasma. Therefore, we subjected commercial recombinant mu rSAA3 to purification to homogeneity via reversed-phase high-performance liquid chromatography (RP-HPLC) and re-assessed its biological potential. RP-HPLC-purified mu rSAA3 did not induce chemokines and lacked in vivo neutrophil chemotactic activity, but retained the capacity to synergize with CXCL8 in the activation of neutrophils. In conclusion, experimental results obtained when using proteins recombinantly expressed in bacteria should always be interpreted with care.
机译:血清淀粉样蛋白A(SAA)基因族是高度保守的,并且编码响应于炎性触发器而上调的急性期蛋白质。多年来,已发表了相当数量的文献,其归因于萨斯,如白细胞募集,细胞因子和趋化因子表达和基质金属蛋白酶的诱导。此外,SaaS还与促象素,亲炎和抗炎作用有关。在这里,我们研究了在大肠杆菌中重组表达的鼠SAA3(MU RSA3)传达的生物学效应。我们观察到在用mu RSAA3刺激单核细胞,肌细胞骨和腹膜细胞后,包括CCl2,CCl3,CXCL1,CXCl2,CXCL6或CXCL8的许多趋化因子的上调。此外,这种SAA变体通过激活TLR4在体内募集中性粒细胞的高效显示。然而,与细菌中的重组表达衍生的蛋白质相关的主要问题是用各种细菌产物的潜在污染,例如脂多糖,脂蛋白和甲型蛋白化肽。这在SAA的情况下是特别的相关性,因为目前在SAA之间存在于重组表达的生物活性和内源源的生物活性差异,即炎症血浆。因此,我们通过反相高效液相色谱(RP-HPLC)使商业重组MU RSAA3进行纯化至均匀性,并重新评估其生物潜力。 RP-HPLC纯化的MU RSAA3没有诱导趋化因子并缺乏体内嗜嗜来自嗜嗜嗜来自嗜嗜中性粒细胞的活性,但保留了在中性粒细胞的激活中用CXCL8进行协同的能力。总之,使用在细菌中重组表达的蛋白质时获得的实验结果应始终用护理解释。

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