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抑制红细胞内蛋白酶体可延缓血红素的生成。

Inhibition of intraerythrocytic proteasome retards the generation of hemorphins.

机构信息

Initiative Project of Translational Medicine, Shandong Academy of Medical Sciences, Jinan 250062, China.

出版信息

Peptides. 2012 Jan;33(1):170-3. doi: 10.1016/j.peptides.2011.11.021. Epub 2011 Dec 2.

DOI:10.1016/j.peptides.2011.11.021
PMID:22154669
Abstract

Hemorphins are a set of hemoglobin-derived opioid peptides. The production mechanism of these structural overlap peptides remains unclear. Based on the sequences of hemorphins, it could be inferred that hemorphins are probably generated by cleavage of hemoglobin β chain at sites favored by the chymotrypsin-like protease. 20S proteasome possesses the chymotrypsin-like activity and still persists in mature erythrocytes. This study attempts to clarify whether the intraerythrocytic proteasome involves in the formation of hemorphins. Hemorphins containing hemorphin-7 and V-hemorphin-7 are isolated by immunoprecipitation from culture supernatant of human erythrocytes. Bortezomib inhibits the chymotrypsin-like activity of intraerythrocytic proteasome and prevents the yield of hemorphins in a dose-dependent manner. The present study suggests that intraerythrocytic proteasome contributes to the generation of hemorphins.

摘要

血红蛋白衍生的阿片样肽是一组血红蛋白衍生的阿片样肽。这些结构重叠肽的产生机制尚不清楚。根据血红蛋白的序列,可以推断血红蛋白可能是由糜蛋白酶样蛋白酶偏好的位点切割血红蛋白β链产生的。20S 蛋白酶体具有糜蛋白酶样活性,并且仍然存在于成熟的红细胞中。本研究试图阐明细胞内蛋白酶体是否参与了血红蛋白的形成。从人红细胞培养上清液中通过免疫沉淀分离含有血红蛋白-7 和 V-血红蛋白-7 的血红蛋白。硼替佐米抑制细胞内蛋白酶体的糜蛋白酶样活性,并以剂量依赖性方式阻止血红蛋白的产生。本研究表明,细胞内蛋白酶体有助于血红蛋白的生成。

相似文献

1
Inhibition of intraerythrocytic proteasome retards the generation of hemorphins.抑制红细胞内蛋白酶体可延缓血红素的生成。
Peptides. 2012 Jan;33(1):170-3. doi: 10.1016/j.peptides.2011.11.021. Epub 2011 Dec 2.
2
Opioid peptides derived from hemoglobin: hemorphins.源自血红蛋白的阿片样肽:血啡肽。
Biopolymers. 1997;43(2):75-98. doi: 10.1002/(SICI)1097-0282(1997)43:2<75::AID-BIP2>3.0.CO;2-X.
3
The hemorphins: a new class of opioid peptides derived from the blood protein hemoglobin.血啡肽:一类源自血液蛋白血红蛋白的新型阿片肽。
Biopolymers. 1997;43(2):147-56. doi: 10.1002/(SICI)1097-0282(1997)43:2<147::AID-BIP8>3.0.CO;2-V.
4
Increased expression and altered subunit composition of proteasomes induced by continuous proteasome inhibition establish apoptosis resistance and hyperproliferation of Burkitt lymphoma cells.持续的蛋白酶体抑制诱导的蛋白酶体表达增加和亚基组成改变导致伯基特淋巴瘤细胞的凋亡抗性和过度增殖。
J Cell Biochem. 2008 Jan 1;103(1):270-83. doi: 10.1002/jcb.21405.
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Effect of noncompetitive proteasome inhibition on bortezomib resistance.非竞争性蛋白酶体抑制对硼替佐米耐药性的影响。
J Natl Cancer Inst. 2010 Jul 21;102(14):1069-82. doi: 10.1093/jnci/djq198. Epub 2010 May 26.
6
Cathepsin D is a good candidate for the specific release of a stable hemorphin from hemoglobin in vivo: VV-hemorphin-7.组织蛋白酶D是体内从血红蛋白中特异性释放稳定的血啡肽(VV-血啡肽-7)的良好候选物。
Biochem Biophys Res Commun. 1998 May 29;246(3):719-24. doi: 10.1006/bbrc.1998.8614.
7
Hemorphins: substrates and/or inhibitors of dipeptidyl peptidase IV. Hemorphins N-terminus sequence influence on the interaction between hemorphins and DPPIV.血红素吗啡:二肽基肽酶IV的底物和/或抑制剂。血红素吗啡N端序列对血红素吗啡与二肽基肽酶IV相互作用的影响。
Biochimie. 2004 Jan;86(1):31-7. doi: 10.1016/j.biochi.2003.11.001.
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Point mutation of the proteasome beta5 subunit gene is an important mechanism of bortezomib resistance in bortezomib-selected variants of Jurkat T cell lymphoblastic lymphoma/leukemia line.蛋白酶体β5亚基基因的点突变是硼替佐米选择的人急性T淋巴细胞白血病细胞系中硼替佐米耐药的重要机制。
J Pharmacol Exp Ther. 2008 Aug;326(2):423-31. doi: 10.1124/jpet.108.138131. Epub 2008 May 23.
9
Proteasome inhibitors: poisons and remedies.蛋白酶体抑制剂:毒药与解药。
Med Res Rev. 2008 Mar;28(2):309-27. doi: 10.1002/med.20111.
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BCL-2 family regulation by the 20S proteasome inhibitor bortezomib.20S蛋白酶体抑制剂硼替佐米对BCL-2家族的调控
Oncogene. 2008 Feb 21;27(9):1189-97. doi: 10.1038/sj.onc.1210744. Epub 2007 Sep 10.

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