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本文引用的文献

1
A novel nano-immunoassay method for quantification of proteins from CD138-purified myeloma cells: biological and clinical utility.一种用于从 CD138 纯化骨髓瘤细胞中定量检测蛋白质的新型纳米免疫分析方法:生物学和临床应用。
Haematologica. 2018 May;103(5):880-889. doi: 10.3324/haematol.2017.181628. Epub 2018 Mar 15.
2
DEPTOR maintains plasma cell differentiation and favorably affects prognosis in multiple myeloma.DEPTOR维持浆细胞分化并对多发性骨髓瘤的预后产生有利影响。
J Hematol Oncol. 2017 Apr 18;10(1):92. doi: 10.1186/s13045-017-0461-8.
3
Comparison and optimization of methods for the simultaneous extraction of DNA, RNA, proteins, and metabolites.同时提取DNA、RNA、蛋白质和代谢物方法的比较与优化
Anal Biochem. 2016 Sep 1;508:25-33. doi: 10.1016/j.ab.2016.05.011. Epub 2016 May 27.
4
Simultaneously extracting DNA, RNA, and protein using kits: is sample quantity or quality prejudiced?同时使用试剂盒提取 DNA、RNA 和蛋白质:样品数量或质量是否受到影响?
Anal Biochem. 2013 Feb 1;433(1):10-8. doi: 10.1016/j.ab.2012.10.006. Epub 2012 Oct 12.
5
A reagent for the single-step simultaneous isolation of RNA, DNA and proteins from cell and tissue samples.一种用于从细胞和组织样本中一步同时分离RNA、DNA和蛋白质的试剂。
Biotechniques. 1993 Sep;15(3):532-4, 536-7.

用于定量分析从CD138纯化的骨髓瘤细胞中蛋白质的毛细管纳米免疫测定法。

Capillary Nano-immunoassay for Quantification of Proteins from CD138-purified Myeloma Cells.

作者信息

Misiewicz-Krzeminska Irena, Isidro Isabel, Gutiérrez Norma C

机构信息

The Institute for Biomedical Research (IBSAL), Salamanca 37007, Spain.

Cancer Research Center-IBMCC (USAL-CSIC), Salamanca 37007, Spain.

出版信息

Bio Protoc. 2019 Jun 20;9(12):e3267. doi: 10.21769/BioProtoc.3267.

DOI:10.21769/BioProtoc.3267
PMID:33654787
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7854265/
Abstract

Protein analysis in bone marrow samples from patients with multiple myeloma (MM) has been limited by the low concentration of proteins obtained after CD138 cell selection. A novel approach based on capillary nano-immunoassay could make it possible to quantify dozens of proteins from each CD138 purified MM sample in an automated manner. Up to now, the knowledge of protein level in those cells was limited because a relatively small quantity of sample is available after the diagnostic procedure. Moreover, the sample often is required for nucleic acids analysis. We have developed the procedure for obtaining proteins from bone marrow samples preserved in RLT+ buffer, and we have successfully applied this approach for the quantification of proteins in the setting of patients with MM. Proteins are extracted from RLT+ buffer, the content is quantified by total protein assay with WES machine and finally, the particular protein expression level is evaluated using specific antibodies by capillary nano-immunoassay with WES machine. The present protocol enables us to quantify many proteins from a limited amount of sample, without losing the opportunity to obtain nucleic acids at the same time. Proteins are quantified automatically in an assay with a low probability of human errors, which makes it a useful tool for biomarkers development.

摘要

多发性骨髓瘤(MM)患者骨髓样本中的蛋白质分析一直受到CD138细胞分选后所得蛋白质浓度较低的限制。一种基于毛细管纳米免疫分析的新方法能够以自动化方式对每个经CD138纯化的MM样本中的数十种蛋白质进行定量。到目前为止,由于诊断程序后可获得的样本量相对较少,对这些细胞中蛋白质水平的了解有限。此外,样本通常还需要用于核酸分析。我们已经开发出从保存在RLT +缓冲液中的骨髓样本中获取蛋白质的程序,并已成功将该方法应用于MM患者蛋白质的定量分析。从RLT +缓冲液中提取蛋白质,用WES仪器通过总蛋白测定法定量其含量,最后,使用特异性抗体通过WES仪器的毛细管纳米免疫分析法评估特定蛋白质的表达水平。本方案使我们能够从有限量的样本中定量多种蛋白质,同时又不会失去获取核酸的机会。蛋白质在检测中自动定量,人为误差概率低,这使其成为生物标志物开发的有用工具。