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本文引用的文献

1
Parallel Reaction Monitoring: A Targeted Experiment Performed Using High Resolution and High Mass Accuracy Mass Spectrometry.平行反应监测:一种使用高分辨率和高质量精度质谱进行的靶向实验。
Int J Mol Sci. 2015 Dec 2;16(12):28566-81. doi: 10.3390/ijms161226120.
2
Elucidation of the CHO Super-Ome (CHO-SO) by Proteoinformatics.通过蛋白质信息学阐明中国仓鼠卵巢细胞超级组(CHO-SO)
J Proteome Res. 2015 Nov 6;14(11):4687-703. doi: 10.1021/acs.jproteome.5b00588. Epub 2015 Oct 13.
3
Toward the complete characterization of host cell proteins in biotherapeutics via affinity depletions, LC-MS/MS, and multivariate analysis.通过亲和去除、液相色谱-串联质谱(LC-MS/MS)和多变量分析实现生物治疗药物中宿主细胞蛋白的全面表征。
MAbs. 2015;7(6):1128-37. doi: 10.1080/19420862.2015.1082017. Epub 2015 Aug 20.
4
Quantitative host cell protein analysis using two dimensional data independent LC-MS(E).使用二维数据独立液相色谱-质谱联用(E)进行宿主细胞蛋白定量分析。
Anal Chem. 2015 Sep 15;87(18):9186-93. doi: 10.1021/acs.analchem.5b01377. Epub 2015 Aug 27.
5
Enhanced Detection of Low-Abundance Host Cell Protein Impurities in High-Purity Monoclonal Antibodies Down to 1 ppm Using Ion Mobility Mass Spectrometry Coupled with Multidimensional Liquid Chromatography.使用离子淌度质谱联用多维液相色谱法增强对高纯度单克隆抗体中低丰度宿主细胞蛋白杂质的检测,检测限低至百万分之一。
Anal Chem. 2015 Oct 20;87(20):10283-91. doi: 10.1021/acs.analchem.5b02103. Epub 2015 Sep 10.
6
More similar than different: Host cell protein production using three null CHO cell lines.相似之处多于不同:使用三种无特定蛋白的中国仓鼠卵巢细胞系生产宿主细胞蛋白。
Biotechnol Bioeng. 2015 Oct;112(10):2068-83. doi: 10.1002/bit.25615. Epub 2015 May 12.
7
SWATH enables precise label-free quantification on proteome scale.SWATH技术能够在蛋白质组规模上实现精确的无标记定量分析。
Proteomics. 2015 Apr;15(7):1215-23. doi: 10.1002/pmic.201400270.
8
Quantitation of 47 human tear proteins using high resolution multiple reaction monitoring (HR-MRM) based-mass spectrometry.使用基于高分辨率多反应监测(HR-MRM)的质谱法定量47种人泪液蛋白质。
J Proteomics. 2015 Feb 6;115:36-48. doi: 10.1016/j.jprot.2014.12.002. Epub 2014 Dec 19.
9
Host cell protein testing by ELISAs and the use of orthogonal methods.通过酶联免疫吸附测定法进行宿主细胞蛋白检测以及正交方法的应用。
Biotechnol Bioeng. 2014 Dec;111(12):2367-79. doi: 10.1002/bit.25327. Epub 2014 Sep 10.
10
A mass spectrometry-based approach to host cell protein identification and its application in a comparability exercise.一种基于质谱法的宿主细胞蛋白鉴定方法及其在可比性研究中的应用。
Anal Biochem. 2014 Oct 15;463:1-6. doi: 10.1016/j.ab.2014.06.005. Epub 2014 Jun 17.

一个基于模块化和适应性质谱的平台,用于支持生物工艺开发以实现最佳宿主细胞蛋白清除。

A modular and adaptive mass spectrometry-based platform for support of bioprocess development toward optimal host cell protein clearance.

作者信息

Walker Donald E, Yang Feng, Carver Joseph, Joe Koman, Michels David A, Yu X Christopher

机构信息

a Protein Analytical Chemistry , Genentech, A Member of the Roche Group , South San Francisco , CA , USA.

出版信息

MAbs. 2017 May/Jun;9(4):654-663. doi: 10.1080/19420862.2017.1303023. Epub 2017 Mar 27.

DOI:10.1080/19420862.2017.1303023
PMID:28346045
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5419088/
Abstract

A modular and adaptive mass spectrometry (MS)-based platform was developed to provide fast, robust and sensitive host cell protein (HCP) analytics to support process development. This platform relies on one-dimensional ultra-high performance liquid chromatography (1D UHPLC) combined with several different MS data acquisition strategies to meet the needs of purification process development. The workflow was designed to allow HCP composition and quantitation for up to 20 samples per day, a throughput considered essential for real time bioprocess development support. With data-dependent acquisition (DDA), the 1D UHPLC-MS/MS method had excellent speed and demonstrated robustness in detecting unknown HCPs at ≥ 50 ng/mg (ppm) level. Combining 1D UHPLC with sequential window acquisition of all theoretical spectra (SWATH) MS enabled simultaneous detection and quantitation of all HCPs in single-digit ng/mg range within 1 hour, demonstrating for the first time the benefit of SWATH MS as a technique for HCP analysis. As another alternative, a targeted MS approach can be used to track the clearance of specific known HCP under various process conditions. This study highlights the importance of designing a robust LC-MS/MS workflow that not only allows HCP discovery, but also affords greatly improved process knowledge and capability in HCP removal. As an orthogonal and complementary detection approach to traditional HCP analysis by enzyme-linked immunosorbent assay, the reported LC-MS/MS workflow supports the development of bioprocesses with optimal HCP clearance and the production of safe and high quality therapeutic biopharmaceuticals.

摘要

开发了一种基于模块化和自适应质谱(MS)的平台,以提供快速、稳健且灵敏的宿主细胞蛋白(HCP)分析,以支持工艺开发。该平台依靠一维超高效液相色谱(1D UHPLC)结合几种不同的MS数据采集策略,以满足纯化工艺开发的需求。工作流程的设计允许每天对多达20个样品进行HCP组成分析和定量,这种通量对于实时生物工艺开发支持而言至关重要。采用数据依赖型采集(DDA)时,1D UHPLC-MS/MS方法速度极快,并且在检测≥50 ng/mg(ppm)水平的未知HCP时表现出稳健性。将1D UHPLC与所有理论谱图的顺序窗口采集(SWATH)MS相结合,能够在1小时内同时检测和定量单位数ng/mg范围内的所有HCP,首次证明了SWATH MS作为一种HCP分析技术的优势。作为另一种选择,可以使用靶向MS方法来跟踪特定已知HCP在各种工艺条件下的清除情况。本研究强调了设计稳健的LC-MS/MS工作流程的重要性,该流程不仅能实现HCP的发现,还能极大地提升对HCP去除的工艺认知和能力。作为一种与传统酶联免疫吸附测定法进行HCP分析的正交且互补的检测方法,所报道的LC-MS/MS工作流程有助于开发具有最佳HCP清除效果的生物工艺,并生产安全、高质量的治疗性生物药物。