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使用“快速 Western 印迹”方法进行蛋白质定量。

Protein Quantification Using the "Rapid Western Blot" Approach.

机构信息

Medizinisches Proteom-Center (MPC), Medical Faculty, Ruhr-University Bochum, Bochum, Germany.

Medical Proteome Analysis, Center for Proteindiagnostics (PRODI), Ruhr-University Bochum, Bochum, Germany.

出版信息

Methods Mol Biol. 2021;2228:29-39. doi: 10.1007/978-1-0716-1024-4_3.

Abstract

For the quantification of certain proteins of interest within a complex sample, Western blot analysis is the most widely used method. It enables detection of a target protein based on the use of specific antibodies. However, the whole procedure is often very time-consuming. Nevertheless, with the development of fast blotting systems and further development of immunostaining methods, a reduction of the processing time can be achieved. Major challenges for the reliable protein quantification by Western blotting are adequate data normalization and stable protein detection. Usually, normalization of the target protein signal is performed based on housekeeping proteins (e.g., glyceraldehyde 3-phosphate dehydrogenase, ß-actin) with the assumption that those proteins are expressed constitutively at the same level across experiments. However, several studies have already shown that this is not always the case making this approach suboptimal. Another strategy uses total protein normalization where the abundance of the target protein is related to the total protein amount in each lane. This approach is independent of a single loading control, and precision of quantification and reliability is increased. For Western blotting several detection methods are available, e.g., colorimetric, chemiluminescent, radioactive, fluorescent detection. Conventional colorimetric staining tends to suffer from low sensitivity, limited dynamic range, and low reproducibility. Chemiluminescence-based methods are straightforward, but the detected signal does not linearly correlate to protein abundance (from protein amounts >5μg) and have a relatively narrow dynamic range. Radioactivity is harmful to health. To overcome these limitations, stain-free methods were developed allowing the combination of fluorescent standards and a stain-free fluorescence-based visualization of total protein in gels and after transfer to the membrane. Here, we present a rapid Western blot protocol, which combines fast blotting using the iBlot system and fast immunostaining utilizing ReadyTector all-in-one solution with the Smart Protein Layers (SPL) approach.

摘要

对于复杂样本中特定感兴趣蛋白的定量分析,Western blot 分析是最广泛使用的方法。它基于使用特定抗体来检测靶蛋白。然而,整个过程通常非常耗时。尽管如此,随着快速印迹系统的发展和免疫染色方法的进一步发展,可以实现处理时间的缩短。Western blot 可靠进行蛋白定量的主要挑战是充分的数据归一化和稳定的蛋白检测。通常,靶蛋白信号的归一化是基于管家蛋白(例如,甘油醛 3-磷酸脱氢酶、β-肌动蛋白)进行的,假设这些蛋白在实验中以相同的水平持续表达。然而,已有多项研究表明,情况并非总是如此,这使得这种方法并不理想。另一种策略是使用总蛋白归一化,其中靶蛋白的丰度与每个泳道中的总蛋白量相关。这种方法不依赖于单一的加载对照,从而提高了定量的精度和可靠性。Western blot 有多种检测方法,例如比色法、化学发光法、放射性、荧光检测。传统的比色染色往往存在灵敏度低、动态范围有限和重现性差的问题。基于化学发光的方法简单直接,但检测到的信号与蛋白丰度(蛋白量>5μg)不成线性相关,且动态范围相对较窄。放射性对健康有害。为了克服这些限制,开发了无染色方法,可以将荧光标准品与无染色荧光凝胶和转膜后的总蛋白可视化相结合。在这里,我们提出了一种快速 Western blot 方案,该方案结合了 iBlot 系统的快速印迹和 ReadyTector all-in-one 溶液的快速免疫染色,以及 Smart Protein Layers(SPL)方法。

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