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利用纤维蛋白原微阵列同时测定两种转谷氨酰胺酶同工酶、凝血因子 XIII 和转谷氨酰胺酶 2 的活性。

Simultaneous activity assay of two transglutaminase isozymes, blood coagulation factor XIII and transglutaminase 2, by use of fibrinogen arrays.

机构信息

Department of Molecular and Cellular Biochemistry and Institute of Medical Science, Kangwon National University School of Medicine, Chuncheon, Kangwon-Do, South Korea.

出版信息

Anal Chem. 2011 Nov 15;83(22):8718-24. doi: 10.1021/ac202178g. Epub 2011 Oct 21.

Abstract

We developed an on-chip activity assay system to simultaneously determine the transamidating activities of blood coagulation factor XIII (FXIII) and transglutaminase 2 (TG2) by use of fibrinogen arrays. FXIII and TG2 are transglutaminase family members that are involved in various physiological functions, including vascular pathophysiology, bone development, and cancer progression. However, investigation of their differential functions is limited by the lack of high-throughput and isozyme-specific activity assays. For the on-chip activity assay, we fabricated protein arrays by immobilizing fibrinogen onto the 3-aminopropyltrimethoxysilane surface of well-type arrays, and we determined transamidating activity by probing biotinylated fibrinogen with Cy3-conjugated streptavidin on arrays. We optimized assay conditions, such as buffer pH, concentrations of dithiothreitol and 5-(biotinamido)pentylamine, and incubation time, and we created equations to determine specific FXIII and TG2 activities in samples. We successfully applied this assay system to monitor changes in FXIII and TG2 activities in THP-1 monocytic cells differentiated with phorbol 12-myristate13-acetate and interleukin-4. This activity assay is sensitive and suitable for high-throughput determination of FXIII and TG2 activities and thus has a strong potential for investigating the differential functions of these isozymes in cell signaling and cardiovascular pathophysiology research.

摘要

我们开发了一种芯片上的活性测定系统,通过使用纤维蛋白原阵列同时测定血液凝固因子 XIII (FXIII) 和转谷氨酰胺酶 2 (TG2) 的转酰胺活性。FXIII 和 TG2 是转谷氨酰胺酶家族的成员,参与多种生理功能,包括血管病理生理学、骨发育和癌症进展。然而,由于缺乏高通量和同工酶特异性活性测定方法,对它们的差异功能的研究受到限制。在芯片上的活性测定中,我们通过将纤维蛋白原固定在井型阵列的 3-氨丙基三甲氧基硅烷表面上来制造蛋白质阵列,并通过在阵列上用 Cy3 缀合的链霉亲和素探测生物素化纤维蛋白原来测定转酰胺活性。我们优化了测定条件,例如缓冲液 pH 值、二硫苏糖醇和 5-(生物素氨基)戊基胺的浓度以及孵育时间,并创建了用于确定样品中特定 FXIII 和 TG2 活性的方程。我们成功地将该测定系统应用于监测用佛波醇 12-肉豆蔻酸 13-乙酸酯和白细胞介素 4 分化的 THP-1 单核细胞中 FXIII 和 TG2 活性的变化。该活性测定方法灵敏且适用于 FXIII 和 TG2 活性的高通量测定,因此在研究这些同工酶在细胞信号转导和心血管病理生理学研究中的差异功能方面具有很大的潜力。

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