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A Novel Approach for Purification and Selective Capture of Membrane Vesicles of the Periodontopathic Bacterium Porphyromonas gingivalis: Membrane Vesicles Bind to Magnetic Beads Coated with Epoxy Groups in a Noncovalent Species-Specific Manner

机译:一种纯化和选择性捕获牙周病性细菌牙龈卟啉单胞菌的膜囊泡的新方法:膜囊泡以非共价物种特异性的方式与涂有环氧基团的磁珠结合

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摘要

Membrane vesicles (MVs) of Porphyromonas gingivalis are regarded as an offensive weapon of the bacterium, leading to tissue deterioration in periodontal disease. Therefore, isolation of highly purified MVs is indispensable to better understand the pathophysiological role of MVs in the progression of periodontitis. MVs are generally isolated by a conventional method based on ultracentrifugation of the bacterial culture supernatant. However, the resulting MVs are often contaminated with co-precipitating bacterial appendages sheared from the live bacteria. Here, we report an intriguing property of P. gingivalis MVs–their ability to bind superparamagnetic beads coated with epoxy groups (SB-Epoxy). Analysis of fractions collected during the purification revealed that all MVs of five tested P. gingivalis stains bound to SB-Epoxy. In contrast, free fimbriae in the crude MV preparation did not bind to the SB-Epoxy. The SB-Epoxy-bound MVs were easily dissociated from the SB-Epoxy using a mild denaturation buffer. These results suggest that the surface chemistry conferred by epoxy on the beads is responsible for the binding, which is mediated by noncovalent bonds. Both the structural integrity and purity of the isolated MVs were confirmed by electron microscopy. The isolated MVs also caused cell detachment from culture dishes at a physiologically relevant concentration. Assays of competitive binding between the SB-Epoxy and mixtures of MVs from five bacterial species demonstrated that only P. gingivalis MVs could be selectively eliminated from the mixtures. We suggest that this novel approach enables efficient purification and selective elimination of P. gingivalis MVs.
机译:牙龈卟啉单胞菌的膜囊泡(MVs)被认为是细菌的攻击性武器,导致牙周疾病的组织恶化。因此,高纯度MV的分离对于更好地了解MV在牙周炎进展中的病理生理作用是必不可少的。通常通过基于细菌培养物上清液超速离心的常规方法分离MV。但是,所得的MV经常被从活菌中剪切下来的共沉淀细菌附肢所污染。在这里,我们报道了牙龈卟啉单胞菌MVs的一个有趣特性,即它们结合涂有环氧基团(SB-环氧)的超顺磁珠的能力。对纯化过程中收集的馏分的分析表明,五个测试的牙龈卟啉单胞菌染色剂的所有MV均与SB-环氧结合。相反,粗制MV制剂中的游离菌毛不与SB-环氧结合。使用温和的变性缓冲液可以轻松地将SB-环氧结合的MVs与SB-环氧解离。这些结果表明,在小珠上由环氧树脂赋予的表面化学作用是由非共价键介导的结合的原因。分离的MV的结构完整性和纯度均通过电子显微镜确认。分离出的MV还导致细胞从生理相关浓度的培养皿中脱离。 SB-环氧与来自五个细菌物种的MV混合物之间的竞争性结合测定表明,只有牙龈卟啉单胞菌MV可以从混合物中选择性清除。我们建议这种新颖的方法能够有效地纯化和选择性消除牙龈卟啉单胞菌MV。

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