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基于常见参考的串联质量标签多重分析用于肽的相对定量:在白喉类毒素降解组分析中的设计与应用。

Common Reference-Based Tandem Mass Tag Multiplexing for the Relative Quantification of Peptides: Design and Application to Degradome Analysis of Diphtheria Toxoid.

机构信息

Division of BioTherapeutics, Leiden Academic Centre for Drug Research (LACDR), Leiden University, 2333 CC Leiden, The Netherlands.

Intravacc, Institute for Translational Vaccinology, 3721 MA Bilthoven, The Netherlands.

出版信息

J Am Soc Mass Spectrom. 2021 Jun 2;32(6):1490-1497. doi: 10.1021/jasms.1c00070. Epub 2021 May 13.

Abstract

Currently, animal tests are being used to confirm the potency and lack of toxicity of toxoid vaccines. In a consistency approach, animal tests could be replaced if production consistency (compared to known good products) can be proven in a panel of in vitro assays. By mimicking the in vivo antigen processing in a simplified in vitro approach, it may be possible to distinguish aberrant products from good products. To demonstrate this, heat-exposed diphtheria toxoid was subjected to partial digestion by cathepsin S (an endoprotease involved in antigen processing), and the peptide formation/degradation kinetics were mapped for various heated toxoids. To overcome the limitations associated with the very large number of samples, we used common reference-based tandem mass tag (TMT) labeling. Instead of using one label per condition with direct comparison between the set of labels, we compared multiple labeled samples to a common reference (a pooled sample containing an aliquot of each condition). In this method, the number of samples is not limited by the number of unique TMT labels. This TMT multiplexing strategy allows for a 15-fold reduction of analysis time while retaining the reliability advantage of TMT labeling over label-free quantification. The formation of the most important peptides could be followed over time and compared among several conditions. The changes in enzymatic degradation kinetics of diphtheria toxoid revealed several suitable candidate peptides for use in a quality control assay that can distinguish structurally aberrant diphtheria toxoid from compliant toxoids.

摘要

目前,正在通过动物试验来确认类毒素疫苗的效力和无毒性。如果可以在一组体外检测中证明生产一致性(与已知的良好产品相比),则可以采用一致性方法来替代动物试验。通过在简化的体外方法中模拟体内抗原处理,可能可以区分异常产品和良好产品。为了证明这一点,对热暴露的白喉类毒素进行了组织蛋白酶 S(一种参与抗原加工的内肽酶)的部分消化,并且针对各种加热的类毒素映射了肽形成/降解的动力学。为了克服与大量样本相关的限制,我们使用了常见的基于参考的串联质量标签(TMT)标记。我们没有使用每个条件一个标签,并在一组标签之间进行直接比较,而是将多个标记的样本与一个共同的参考(包含每个条件的等分试样的混合样本)进行比较。在这种方法中,样本数量不受唯一 TMT 标签数量的限制。这种 TMT 多重化策略允许将分析时间减少 15 倍,同时保留 TMT 标记相对于无标记定量的可靠性优势。可以随时间跟踪最重要的肽的形成并在几种条件之间进行比较。白喉类毒素的酶降解动力学的变化揭示了几个适合用作质量控制测定的候选肽,该测定可将结构异常的白喉类毒素与合规的类毒素区分开。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed88/8176455/1dd0459b9d39/js1c00070_0001.jpg

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