生物
热休克蛋白
蛋白质组学
分子生物学
热休克蛋白70
生物化学
基因
作者
Youngbin Lim,Bo‐Jeong Pyun,Hae‐June Lee,Sang‐Rok Jeon,Yeung Bae Jin,Yun‐Sil Lee
出处
期刊:Proteomics
[Wiley]
日期:2011-02-09
卷期号:11 (7): 1254-1263
被引量:23
标识
DOI:10.1002/pmic.201000332
摘要
Abstract Increasing efforts are being made to develop more sensitive and faster molecular methodologies at the genomic and proteomic levels for the identification of protein markers after exposure to ionizing radiation (IR). However, few specific protein markers, especially organ‐specific markers, have been identified. In this study, we analyzed altered protein expressions in various tissues, namely, brain, lung, spleen, and intestine, from 1 Gy‐irradiated mice by employing 2‐DE analysis. MALDI‐TOF MS and peptide mapping identified 25 proteins that showed greater than twofold expressional changes. In order to confirm significant differences between control and IR‐treated samples, ten identified proteins with available commercial antibodies were selected for immunoblotting. Of these, only five showed protein expression patterns that were similar to 2‐DE data. These were heat shock protein 5 (HSP 5), HSP 90 kDa β, HSP 1, transaldolase 1 (TA1), and phosphoglycerate kinase 1 (PGK1). In particular, PGK1 was specifically upregulated in mouse intestine, and TA1 was specifically downregulated in brain by irradiation. TA1 expression was unaltered in other tissues. Based on these data, we suggest that TA1 and PGK1 can be considered as candidate tissue‐specific protein markers of IR exposure.
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