Biomolecular Mass Spectrometry & Proteomics, Bijvoet Center for Biomolecular Research & Utrecht Institute for Pharmaceutical Sciences, Utrecht University, Padualaan 8, 3584 CH Utrecht, The Netherlands.
Netherlands Proteomics Center, Padualaan 8, 3584 CH Utrecht, The Netherlands.
J Am Soc Mass Spectrom. 2024 Jun 5;35(6):1292-1300. doi: 10.1021/jasms.4c00076. Epub 2024 Apr 25.
Endogenous antibodies, or immunoglobulins (Igs), abundantly present in body fluids, represent some of the most challenging samples to analyze, largely due to the immense variability in their sequences and concentrations. It has been estimated that our body can produce billions of different Ig proteins with different isotypes, making their individual analysis seemingly impossible. However, recent advances in protein-centric proteomics using LC-MS coupled to Orbitrap mass analyzers to profile intact Fab fragments formed by selective cleavage at the IgG-hinge revealed that IgG repertoires may be less diverse, albeit unique for each donor. Serum repertoires seem to be dominated by a few hundred clones that cumulatively make up 50-95% of the total IgG content. Enabling such analyses required careful optimization of the chromatography and mass analysis, as all Fab analytes are highly alike in mass (46-51 kDa) and sequence. To extend the opportunities of this mass-spectrometry-based profiling of antibody repertoires, we here report the optimization and evaluation of an alternative MS platform, namely, the timsTOF, for antibody repertoire profiling. The timsTOF mass analyzer has gained traction in recent years for peptide-centric proteomics and found wide applicability in plasma proteomics, affinity proteomics, and HLA peptidomics, to name a few. However, for protein-centric analysis, this platform has been less explored. Here, we demonstrate that the timsTOF platform can be adapted to perform protein-centric LC-MS-based profiling of antibody repertoires. In a side-by-side comparison of the timsTOF and the Orbitrap we demonstrate that the extracted serum antibody repertoires are alike qualitatively and quantitatively, whereby in particular the sensitivity of the timsTOF platform excels. Future incorporation of advanced top-down capabilities on the timsTOF may make this platform a very valuable alternative for protein-centric proteomics and top-down proteomics and thus also for personalized antibody repertoire profiling.
内源性抗体,又称免疫球蛋白(Ig),在体液中大量存在,是最难分析的样本之一,主要是因为它们的序列和浓度存在巨大的可变性。据估计,我们的身体可以产生数十亿种不同的 Ig 蛋白,具有不同的同种型,这使得对它们进行单独分析似乎是不可能的。然而,最近使用 LC-MS 结合轨道阱质谱仪对完整 Fab 片段进行分析的蛋白质组学方法的进展表明,IgG 库可能没有那么多样化,尽管对每个供体来说都是独特的。血清库似乎由几百个克隆组成,这些克隆累积起来占总 IgG 含量的 50-95%。要实现这种分析,需要仔细优化色谱和质谱分析,因为所有 Fab 分析物在质量(46-51 kDa)和序列上都非常相似。为了扩展这种基于质谱的抗体库分析的机会,我们在此报告了一种替代 MS 平台,即 timsTOF,用于抗体库分析的优化和评估。timsTOF 质谱仪近年来在肽组学中得到了广泛应用,并在血浆蛋白质组学、亲和蛋白质组学和 HLA 肽组学等方面得到了广泛的应用。然而,对于蛋白质组学分析,这个平台的应用较少。在这里,我们证明了 timsTOF 平台可以适应基于 LC-MS 的蛋白质组学抗体库分析。我们在 timsTOF 和 Orbitrap 的平行比较中证明,提取的血清抗体库在质量和数量上是相似的,特别是 timsTOF 平台的灵敏度非常出色。未来在 timsTOF 上加入先进的自上而下的能力可能会使这个平台成为蛋白质组学和自上而下的蛋白质组学以及个性化抗体库分析的一个非常有价值的替代方案。