In:
ChemBioChem, Wiley, Vol. 9, No. 8 ( 2008-05-23), p. 1251-1259
Abstract:
Ku is a predominantly nuclear protein that functions as a DNA double‐strand‐break (DSB) binding protein and regulatory subunit of the DNA‐dependent protein kinase (DNA‐PK). DNA‐PK is involved in synapsis and remodeling of broken DNA ends during nonhomologous end‐joining (NHEJ) of DNA DSBs. It has also recently been demonstrated that Ku plays roles in cytoplasmic and membrane processes, namely: interaction with matrix metalloproteinase 9, acting as a co‐receptor for parvoviral infection, and also interacting with cell polarity protein, Par3. We present a method for creating stable expression of Ku‐eGFP in CHO cells and extend the procedure to purify Ku‐eGFP for in vitro assaying. We demonstrated that Ku‐eGFP localizes to the nucleus of HeLa cells upon microinjection into the cytoplasm as well as localizing to laser induced DNA damage. We also characterized the diffusional dynamics of Ku in the nucleus and in the cytoplasm using fluorescence correlation spectroscopy (FCS). The FCS data suggest that whereas the majority of Ku (70 %) in the nucleus is mobile and freely diffusing, in a cellular context, there also exists a significant slow process fraction (30 %). Strikingly, in the cytoplasm, this immobile/slow moving fraction is even more pronounced (45 %).
Type of Medium:
Online Resource
ISSN:
1439-4227
,
1439-7633
DOI:
10.1002/cbic.200700750
Language:
English
Publisher:
Wiley
Publication Date:
2008
detail.hit.zdb_id:
2020469-3
SSG:
12
