Li Fengping, Hooper Andrea T, Golas Jonathon, Chang Chao-Pei Betty, Neubert Hendrik, King Lindsay
BioMedicine Design, Pfizer Inc., 1 Burtt Road, Andover, Massachusetts 01810, United States.
Oncology Research & Development, Pfizer Inc., 401 N Middletown Rd, Pearl River, New York 10965, United States.
J Proteome Res. 2022 Oct 7;21(10):2331-2340. doi: 10.1021/acs.jproteome.2c00182. Epub 2022 Sep 1.
The fibronectin (FN) isoform including the extradomain B (EDB) segment (EDB + FN) is a promising tumor target and is highly expressed in some tumor types, such as breast, head, and neck cancer. To date, mostly immunohistochemistry (IHC) and Western blot have been used for the analysis of EDB + FN. However, complete quantitative measurements of EDB + FN expression in a tumor and circulation are important for the development of anti-EDB therapeutics. To this end, a method using protein enrichment followed by online antipeptide antibody enrichment coupled with a nanoflow LC-MS/MS was developed to quantify EDB + FN in human and cynomolgus plasma, patient-derived xenograft (PDX) tumors, and PDX formalin-fixed paraffin-embedded (FFPE) samples. Mouse plasma EDB + FN was analyzed using a protein immunoaffinity method followed by nanoflow LC-MS/MS. EDB + FN concentrations were 63.1 pmol/g in PDX breast cancer tumor and 49.6 pmol/g in PDX head and neck tumor. Mean plasma concentration was 1.1 nM (pmol/mL, 47.4 ng/mL) in normal healthy humans and 0.35 nM (15.1 ng/mL) in naive cynomolgus. The assay sensitivity was 0.018 nM based on calibration with recombinant human EDB + FN (rhEDB + FN).
包含额外结构域B(EDB)片段的纤连蛋白(FN)异构体(EDB + FN)是一种很有前景的肿瘤靶点,在某些肿瘤类型中高表达,如乳腺癌、头颈癌。迄今为止,主要使用免疫组织化学(IHC)和蛋白质印迹法来分析EDB + FN。然而,对肿瘤和循环中EDB + FN表达进行完整的定量测量对于抗EDB治疗药物的开发很重要。为此,开发了一种先进行蛋白质富集,然后在线进行抗肽抗体富集并结合纳流液相色谱-串联质谱(LC-MS/MS)的方法,以定量人血浆和食蟹猴血浆、患者来源异种移植瘤(PDX)肿瘤以及PDX福尔马林固定石蜡包埋(FFPE)样本中的EDB + FN。使用蛋白质免疫亲和法结合纳流LC-MS/MS分析小鼠血浆中的EDB + FN。PDX乳腺癌肿瘤中EDB + FN浓度为63.1 pmol/g,PDX头颈肿瘤中为49.6 pmol/g。正常健康人的平均血浆浓度为1.1 nM(pmol/mL,47.4 ng/mL),未接触过抗原的食蟹猴为0.35 nM(15.1 ng/mL)。基于重组人EDB + FN(rhEDB + FN)校准,该检测方法的灵敏度为0.018 nM。