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流感病毒样颗粒的通用无标记过程中定量分析。

Universal label-free in-process quantification of influenza virus-like particles.

作者信息

Carvalho Sofia B, Moleirinho Mafalda G, Wheatley David, Welsh John, Gantier René, Alves Paula M, Peixoto Cristina, Carrondo Manuel J T

机构信息

iBET, Instituto de Biologia Experimental e Tecnológica, Oeiras, Portugal.

Instituto de Tecnologia Química e Biológica António Xavier, Universidade Nova de Lisboa, Oeiras, Portugal.

出版信息

Biotechnol J. 2017 Aug;12(8). doi: 10.1002/biot.201700031. Epub 2017 Jul 5.

Abstract

Virus-like particles (VLPs) are becoming established as vaccines, in particular for influenza pandemics, increasing the interest in the development of VLPs manufacturing bioprocess. However, for complex VLPs, the analytical tools used for quantification are not yet able to keep up with the bioprocess progress. Currently, quantification for Influenza relies on traditional methods: hemagglutination assay or Single Radial Immunodiffusion. These analytical technologies are time-consuming, cumbersome, and not supportive of efficient downstream process development and monitoring. Hereby we report a label-free tool that uses Biolayer interferometry (BLI) technology applied on an Octet platform to quantify Influenza VLPs at all stages of bioprocess. Human (α2,6-linked sialic acid) and avian (α2,3-linked sialic acid) biotinylated receptors associated with streptavidin biosensors were used, to quantify hemagglutinin content in several mono- and multivalent Influenza VLPs. The applied method was able to quantify hemagglutinin from crude samples up to final bioprocessing VLP product. BLI technology confirmed its value as a high throughput analytical tool with high sensitivity and improved detection limits compared to traditional methods. This simple and fast method allowed for real-time results, which are crucial for in-line monitoring of downstream processing, improving process development, control and optimization.

摘要

病毒样颗粒(VLPs)正逐渐成为疫苗,尤其是针对流感大流行的疫苗,这增加了人们对开发VLPs生产生物工艺的兴趣。然而,对于复杂的VLPs,用于定量的分析工具还无法跟上生物工艺的进展。目前,流感病毒的定量依赖于传统方法:血凝试验或单向辐射免疫扩散法。这些分析技术耗时、繁琐,不利于高效的下游工艺开发和监测。在此,我们报告一种无标记工具,该工具利用应用于Octet平台的生物层干涉术(BLI)技术,在生物工艺的各个阶段对流感病毒VLPs进行定量。使用与链霉亲和素生物传感器相关的人源(α2,6-连接唾液酸)和禽源(α2,3-连接唾液酸)生物素化受体,来定量几种单价和多价流感病毒VLPs中的血凝素含量。所应用的方法能够对从粗样品到最终生物工艺VLP产品中的血凝素进行定量。与传统方法相比,BLI技术证实了其作为一种高通量分析工具的价值,具有高灵敏度和更低的检测限。这种简单快速的方法可实现实时结果,这对于下游工艺的在线监测、改进工艺开发、控制和优化至关重要。

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