A distributable LC-MS/MS method for the measurement of serum thyroglobulin

IF 3.1 4区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY Journal of Mass Spectrometry and Advances in the Clinical Lab Pub Date : 2022-11-01 DOI:10.1016/j.jmsacl.2022.09.005
Junyan Shi , William S. Phipps , Benjamin Y. Owusu , Clark M. Henderson , Thomas J. Laha , Jessica O. Becker , Morteza Razavi , Michelle A. Emrick , Andrew N. Hoofnagle
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引用次数: 5

Abstract

Background

Despite its clear advantages over immunoassay-based testing, the measurement of serum thyroglobulin by mass spectrometry remains limited to a handful of institutions. Slow adoption by clinical laboratories could reflect limited accessibility to existing methods that have sensitivity comparable to modern immunoassays, as well as a lack of tools for calibration and assay harmonization.

Methods

We developed and validated a liquid chromatography-tandem mass spectrometry-based assay for the quantification of serum thyroglobulin. The protocol combined peptide immunoaffinity purification using a commercially available, well-characterized monoclonal antibody and mobile phase modification with dimethylsulfoxide (DMSO) for enhanced sensitivity. To facilitate harmonization with other laboratories, we developed a novel, serum-based 5-point distributable reference material (Husky Ref).

Results

The assay demonstrated a lower limit of quantification of 0.15 ng/mL (<20 %CV). Mobile phase DMSO increased signal intensity of the target peptide at least 3-fold, improving quantification at low concentrations. Calibration traceable to Husky Ref enabled harmonization between laboratories in an interlaboratory study.

Conclusions

Sensitive mass spectrometry-based thyroglobulin measurement can be achieved using a monoclonal antibody during peptide immunoaffinity purification and the addition of mobile phase DMSO. Laboratories interested in deploying this assay can utilize the provided standard operating procedure and freely-available Husky Ref reference material.

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可分配LC-MS/MS法测定血清甲状腺球蛋白
背景:尽管质谱法比基于免疫分析的检测有明显的优势,但它仍然局限于少数机构。临床实验室采用缓慢可能反映了现有方法的可及性有限,这些方法具有与现代免疫测定相当的敏感性,以及缺乏校准和测定统一的工具。方法建立并验证了一种基于液相色谱-串联质谱的血清甲状腺球蛋白定量分析方法。该方案结合了多肽免疫亲和纯化,使用市售的、特性良好的单克隆抗体和二甲基亚砜(DMSO)的流动相修饰,以提高灵敏度。为了促进与其他实验室的协调,我们开发了一种新的、基于血清的5点可分发参考物质(Husky Ref)。结果该方法的定量下限为0.15 ng/mL (20% CV)。流动相DMSO使目标肽的信号强度增加了至少3倍,在低浓度下提高了定量。校准可追溯到赫斯基Ref使实验室之间的协调实验室间的研究。结论在多肽免疫亲和纯化和加入流动相DMSO的过程中,采用单克隆抗体可实现基于质谱法的甲状腺球蛋白检测。有兴趣部署此分析的实验室可以利用提供的标准操作程序和免费提供的赫斯基参考材料。
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来源期刊
Journal of Mass Spectrometry and Advances in the Clinical Lab
Journal of Mass Spectrometry and Advances in the Clinical Lab Health Professions-Medical Laboratory Technology
CiteScore
4.30
自引率
18.20%
发文量
41
审稿时长
81 days
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