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利用微流控免疫印迹技术进行炎症反应分析。

Profiling inflammatory responses with microfluidic immunoblotting.

机构信息

Michigan Nanotechnology Institute for Medicine and Biological Sciences, University of Michigan, Ann Arbor, Michigan, United States of America.

出版信息

PLoS One. 2013 Nov 27;8(11):e81889. doi: 10.1371/journal.pone.0081889. eCollection 2013.

Abstract

Rapid profiling of signaling pathways has been a long sought after goal in biological sciences and clinical medicine. To understand these signaling pathways, their protein components must be profiled. The protein components of signaling pathways are typically profiled with protein immunoblotting. Protein immunoblotting is a powerful technique but has several limitations including the large sample requirements, high amounts of antibody, and limitations in assay throughput. To overcome some of these limitations, we have designed a microfluidic protein immunoblotting device to profile multiple signaling pathways simultaneously. We show the utility of this approach by profiling inflammatory signaling pathways (NFκB, JAK-STAT, and MAPK) in cell models and human samples. The microfluidic immunoblotting device can profile proteins and protein modifications with 5380-fold less antibody compared to traditional protein immunoblotting. Additionally, this microfluidic device interfaces with commonly available immunoblotting equipment, has the ability to multiplex, and is compatible with several protein detection methodologies. We anticipate that this microfluidic device will complement existing techniques and is well suited for life science applications.

摘要

在生物科学和临床医学中,快速分析信号通路一直是人们长期追求的目标。为了了解这些信号通路,必须对其蛋白质成分进行分析。信号通路的蛋白质成分通常通过蛋白质免疫印迹进行分析。蛋白质免疫印迹是一种强大的技术,但存在几个限制,包括大样本需求、大量抗体和检测通量限制。为了克服这些限制中的一些,我们设计了一种微流控蛋白质免疫印迹设备,可同时分析多个信号通路。我们通过在细胞模型和人类样本中分析炎症信号通路(NFκB、JAK-STAT 和 MAPK)展示了这种方法的实用性。与传统的蛋白质免疫印迹相比,微流控免疫印迹设备使用的抗体少了 5380 倍,可对蛋白质和蛋白质修饰进行分析。此外,这种微流控设备与常用的免疫印迹设备接口兼容,具有多路复用的能力,并且与几种蛋白质检测方法兼容。我们预计这种微流控设备将补充现有的技术,非常适合生命科学应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6302/3842271/d2c4d1edcfeb/pone.0081889.g001.jpg

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