4.8 Article

Real-Time Measurements of Protein Dynamics Using Fluorescence Activation-Coupled Protein Labeling Method

期刊

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 133, 期 17, 页码 6745-6751

出版社

AMER CHEMICAL SOC
DOI: 10.1021/ja200225m

关键词

-

资金

  1. Ministry of Education, Culture, Sports, Science and Technology of Japan (Center of Education and Research for Chemical Biology of the Diseases) [20117003, 19205021, 22000006]
  2. Hoh-ansha Foundation
  3. Japanese Society for the Promotion of Science
  4. Grants-in-Aid for Scientific Research [21500301, 20670002, 20117003] Funding Source: KAKEN

向作者/读者索取更多资源

We present a fluorescence activation-coupled protein labeling (FAPL) method, which employs small-molecular probes that exhibit almost no basal fluorescence but acquire strong fluorescence upon covalent binding to tag-proteins. This method enables real-time imaging of protein labeling without any washout process and is uniquely suitable for real-time imaging of protein dynamics on the cell surface. We applied this method to address the spatiotemporal dynamics of the EGF receptor during cell migration.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据