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最小抗酶肽完全能结合并抑制鸟氨酸脱羧酶和抗酶抑制剂。

Minimal antizyme peptide fully functioning in the binding and inhibition of ornithine decarboxylase and antizyme inhibitor.

机构信息

Department of Life Sciences and Institute of Bioinformatics, National Chung Hsing University, Taichung, Taiwan.

出版信息

PLoS One. 2011;6(9):e24366. doi: 10.1371/journal.pone.0024366. Epub 2011 Sep 9.

Abstract

Antizyme (AZ) is a protein with 228 amino acid residues that regulates ornithine decarboxylase (ODC) by binding to ODC and dissociating its homodimer, thus inhibiting its enzyme activity. Antizyme inhibitor (AZI) is homologous to ODC, but has a higher affinity than ODC for AZ. In this study, we quantified the biomolecular interactions between AZ and ODC as well as AZ and AZI to identify functional AZ peptides that could bind to ODC and AZI and inhibit their function as efficiently as the full-length AZ protein. For these AZ peptides, the inhibitory ability of AZ_95-228 was similar to that of AZ_WT. Furthermore, AZ_95-176 displayed an inhibition (IC(50): 0.20 µM) similar to that of AZ-95-228 (IC(50): 0.16 µM), even though a large segment spanning residues 177-228 was deleted. However, further deletion of AZ_95-176 from either the N-terminus or the C-terminus decreased its ability to inhibit ODC. The AZ_100-176 and AZ_95-169 peptides displayed a noteworthy decrease in ability to inhibit ODC, with IC(50) values of 0.43 and 0.37 µM, respectively. The AZ_95-228, AZ_100-228 and AZ_95-176 peptides had IC(50) values comparable to that of AZ_WT and formed AZ-ODC complexes with K(d,AZ-ODC) values of 1.5, 5.3 and 5.6 µM, respectively. Importantly, our data also indicate that AZI can rescue AZ peptide-inhibited ODC enzyme activity and that it can bind to AZ peptides with a higher affinity than ODC. Together, these data suggest that these truncated AZ proteins retain their AZI-binding ability. Thus, we suggest that AZ_95-176 is the minimal AZ peptide that is fully functioning in the binding of ODC and AZI and inhibition of their function.

摘要

抗酶(AZ)是一种由 228 个氨基酸残基组成的蛋白质,通过与 ODC 结合并使其同源二聚体解离,从而抑制其酶活性,从而调节鸟氨酸脱羧酶(ODC)。抗酶抑制剂(AZI)与 ODC 同源,但与 AZ 相比,其与 AZ 的亲和力更高。在这项研究中,我们定量测定了 AZ 与 ODC 以及 AZ 与 AZI 之间的生物分子相互作用,以鉴定能够与 ODC 和 AZI 结合并有效抑制其功能的功能性 AZ 肽,其抑制能力与全长 AZ 蛋白相当。对于这些 AZ 肽,AZ_95-228 的抑制能力与 AZ_WT 相似。此外,尽管缺失了 177-228 残基的大片段,但 AZ_95-176 仍显示出类似的抑制作用(IC50:0.20 µM)。然而,进一步从 N 端或 C 端缺失 AZ_95-176 会降低其抑制 ODC 的能力。AZ_100-176 和 AZ_95-169 肽显示出抑制 ODC 的能力明显下降,IC50 值分别为 0.43 和 0.37 µM。AZ_95-228、AZ_100-228 和 AZ_95-176 肽的 IC50 值与 AZ_WT 相当,并分别形成 Kd(AZ-ODC)值为 1.5、5.3 和 5.6 µM 的 AZ-ODC 复合物。重要的是,我们的数据还表明,AZI 可以挽救 AZ 肽抑制的 ODC 酶活性,并且它可以与 AZ 肽结合的亲和力高于 ODC。综上所述,这些数据表明这些截短的 AZ 蛋白保留了与 AZI 结合的能力。因此,我们认为 AZ_95-176 是一种完整的 AZ 肽,它可以完全与 ODC 和 AZI 结合,并抑制它们的功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f81/3170320/4122a6c81ea3/pone.0024366.g001.jpg

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