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SMaRT M-Seq:单克隆丙种球蛋白病中M蛋白测序的优化分步方案。

SMaRT M-Seq: an optimized step-by-step protocol for M protein sequencing in monoclonal gammopathies.

作者信息

Nevone Alice, Lattarulo Francesca, Russo Monica, Cascino Pasquale, Merlini Giampaolo, Palladini Giovanni, Nuvolone Mario

机构信息

Department of Molecular Medicine, University of Pavia, Pavia, 27100, Italy.

Amyloidosis Research and Treatment Center, Fondazione IRCCS Policlinico San Matteo, Pavia, 27100, Italy.

出版信息

Biol Methods Protoc. 2024 Oct 3;9(1):bpae074. doi: 10.1093/biomethods/bpae074. eCollection 2024.

Abstract

In patients with monoclonal gammopathies, tumor B cells or plasma cells secrete a monoclonal antibody (M protein) that not only serves as a biomarker for tumor tracking but can also cause potentially life-threatening organ damage. This damage is driven by the patient-specific sequence of the M protein. Methods for sequencing M proteins have been limited by their high cost and time-consuming nature, and while recent approaches using next-generation sequencing or mass spectrometry offer advancements, they may require tumor cell sorting, are limited to subsets of immunoglobulin genes or patients, and/or lack extensive validation. To address these limitations, we have recently developed a novel method, termed Single Molecule Real-Time Sequencing of the M protein (SMaRT M-Seq), which combines the unbiased amplification of expressed immunoglobulin genes via inverse PCR from circularized cDNA with long-read DNA sequencing, followed by bioinformatic and immunogenetic analyses. This approach enables the unambiguous identification of full-length variable sequences of M protein genes across diverse patient cohorts, including those with low tumor burden. Our protocol has undergone technical validation and has been successfully applied to large patient cohorts with monoclonal gammopathies. Here we present the step-by-step protocol for SMaRT M-Seq. By enabling the parallel sequencing of M proteins from a large number of samples in a cost-effective and time-efficient manner, SMaRT M-Seq facilitates access to patient-specific M protein sequences, advancing personalized medicine approaches and enabling deeper mechanistic studies in monoclonal gammopathies.

摘要

在单克隆丙种球蛋白病患者中,肿瘤B细胞或浆细胞分泌一种单克隆抗体(M蛋白),它不仅可作为肿瘤追踪的生物标志物,还可能导致危及生命的器官损伤。这种损伤是由M蛋白的患者特异性序列驱动的。M蛋白测序方法一直受到高成本和耗时特性的限制,虽然最近使用下一代测序或质谱的方法有了进展,但它们可能需要肿瘤细胞分选,仅限于免疫球蛋白基因的子集或患者,和/或缺乏广泛的验证。为了解决这些限制,我们最近开发了一种新方法,称为M蛋白单分子实时测序(SMaRT M-Seq),它将通过反向PCR从环化cDNA对表达的免疫球蛋白基因进行无偏差扩增与长读长DNA测序相结合,随后进行生物信息学和免疫遗传学分析。这种方法能够明确鉴定不同患者群体中M蛋白基因的全长可变序列,包括那些肿瘤负荷低的患者。我们的方案已经过技术验证,并已成功应用于大量单克隆丙种球蛋白病患者群体。在这里,我们展示了SMaRT M-Seq的详细方案。通过以经济高效且省时的方式对大量样本中的M蛋白进行平行测序,SMaRT M-Seq有助于获取患者特异性M蛋白序列,推动个性化医疗方法的发展,并使单克隆丙种球蛋白病的机制研究更深入。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00a6/11520399/7058ab6a43a3/bpae074f1.jpg

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