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Anti-apoptosis Proteins Mcl-1 and Bcl-xL Have Different p53-Binding Profiles
Yao, H.; Mi, S.; Gong, W.; Lin, J.; Xu, N.; Perrett, S.; . . . Feng, Y.
2013
发表期刊Biochemistry
卷号52期号:37页码:6324-6334
摘要 One of the transcription-independent mechanisms of the tumor suppressor p53 discovered in recent years involves physical interaction between p53 and proteins of the Bcl-2 family. In this paper, significant differences between the interaction of p53 with Mcl-1 and Bcl-xL were demonstrated by NMR spectroscopy and isothermal titration calorimetry. Bcl-xL was found to bind strongly to the p53 DNA-binding domain (DBD) with a dissociation constant (Kd) of ∼600 nM, whereas Mcl-1 binds to the p53 DBD weakly with a dissociation constant in the mM range. In contrast, the p53 transactivation domain (TAD) binds weakly to Bcl-xL with a Kd ∼ 300−500 μM and strongly to Mcl-1 with a Kd ∼ 10−20 μM. NMR titrations indicate that although the p53 TAD binds to the BH3-binding grooves of both Bcl-xL and Mcl-1, Bcl-xL prefers to bind to the first subdomain (TAD1) in the p53 TAD, and Mcl-1 prefers to bind to the second subdomain (TAD2). Therefore, Mcl-1 and Bcl-xL have different p53-binding profiles. This indicates that the detailed interaction mechanisms are different, although both Mcl-1 and BclxLcan mediate transcription-independent cytosolic roles of p53. The revealed differences in binding sites and binding affinities should be considered when BH3 mimetics are used in cancer therapy development.
 
学科领域代谢物组学
收录类别SCI
语种英语
文献类型期刊论文
条目标识符http://ir.qibebt.ac.cn/handle/337004/1687
专题代谢物组学研究组
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GB/T 7714
Yao, H.,Mi, S.,Gong, W.,et al. Anti-apoptosis Proteins Mcl-1 and Bcl-xL Have Different p53-Binding Profiles[J]. Biochemistry,2013,52(37):6324-6334.
APA Yao, H..,Mi, S..,Gong, W..,Lin, J..,Xu, N..,...&. . . Feng, Y..(2013).Anti-apoptosis Proteins Mcl-1 and Bcl-xL Have Different p53-Binding Profiles.Biochemistry,52(37),6324-6334.
MLA Yao, H.,et al."Anti-apoptosis Proteins Mcl-1 and Bcl-xL Have Different p53-Binding Profiles".Biochemistry 52.37(2013):6324-6334.
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