绿色荧光蛋白
蛋白质亚细胞定位预测
维多利亚多管发光水母
亚细胞定位
融合蛋白
转化(遗传学)
细胞生物学
蛋白质标签
格斯报告系统
生物
分子生物学
化学
生物化学
基因
农杆菌
重组DNA
出处
期刊:CSH Protocols
[Cold Spring Harbor Laboratory Press]
日期:2007-02-01
卷期号:2007 (2): pdb.prot4689-pdb.prot4689
被引量:28
摘要
INTRODUCTIONRecombinant tags (i.e., reporter proteins) offer an excellent alternative to antibodies for determining the subcellular localization of proteins. The most user-friendly tags are the ß-glucuronidase (GUS) reporter enzyme from Escherichia coli and fluorescent proteins derived primarily from the green fluorescent protein (GFP) of the jellyfish Aequorea victoria. GUS is useful primarily as a tag to address nuclear localization, whereas GFP is more versatile. Moreover, GFP is detectable directly in living cells, whereas GUS is only detected indirectly by staining of fixed tissue. This may lead to artifacts or it may obscure problems with protein solubility. In this protocol, protein localization is routinely assayed after particle-mediated transient transformation of onion epidermal cells. With this method it can be determined rapidly whether a given fusion protein is active, and preliminary targeting data can be obtained.
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