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通过对带3中38000道尔顿片段进行蛋白水解消化来调节人红细胞膜中的阴离子转运活性。

Anion transport activity in the human erythrocyte membrane modulated by proteolytic digestion of the 38,000-dalton fragment in Band 3.

作者信息

Matsuyama H, Kawano Y, Hamasaki N

出版信息

J Biol Chem. 1983 Dec 25;258(24):15376-81.

PMID:6654917
Abstract

Extracellular treatment of human erythrocytes with papain completely converted the chymotryptic 38,000-dalton fragment of Band 3 to the 29,000-dalton fragment and inhibited the transport of inorganic phosphate in the cells. The inhibition, however, was not complete, indicating the presence of two components in the anion-transport system: the one resistant to papain digestion and the other sensitive to the digestion. The latter activity is well correlated with the degradation of the 38,000-dalton fragment. The activity remaining in the cells treated with papain was markedly different from that of the control cells. The remaining activity was not inhibited by pyridoxal phosphate and dinitrostilbene-2,2'-disulfonic acid, potent inhibitors to the anion transport, whereas phenyl phosphate inhibited the activities of both papain-treated and control cells. The results indicate that the anion-transport system consists of multiple anion-binding sites and a part of the system which is sensitive to pyridoxal phosphate and dinitrostilbene-2,2'-disulfonic acid was located in the papain-sensitive portion of 38,000-dalton fragment. A possible model of the anion-transport system was presented.

摘要

用木瓜蛋白酶对人红细胞进行细胞外处理,可使带3的胰凝乳蛋白酶作用产生的38000道尔顿片段完全转化为29000道尔顿片段,并抑制细胞中无机磷酸的转运。然而,这种抑制并不完全,这表明阴离子转运系统中存在两种成分:一种对木瓜蛋白酶消化有抗性,另一种对消化敏感。后一种活性与38000道尔顿片段的降解密切相关。用木瓜蛋白酶处理的细胞中剩余的活性与对照细胞的活性明显不同。剩余活性不受阴离子转运的有效抑制剂磷酸吡哆醛和二硝基芪-2,2'-二磺酸的抑制,而磷酸苯酯则抑制木瓜蛋白酶处理细胞和对照细胞的活性。结果表明,阴离子转运系统由多个阴离子结合位点组成,对磷酸吡哆醛和二硝基芪-2,2'-二磺酸敏感的系统部分位于38000道尔顿片段的木瓜蛋白酶敏感部分。提出了阴离子转运系统的一种可能模型。

相似文献

1
Anion transport activity in the human erythrocyte membrane modulated by proteolytic digestion of the 38,000-dalton fragment in Band 3.通过对带3中38000道尔顿片段进行蛋白水解消化来调节人红细胞膜中的阴离子转运活性。
J Biol Chem. 1983 Dec 25;258(24):15376-81.
2
Anion transport across the erythrocyte membrane, in situ proteolysis of band 3 protein, and cross-linking of proteolytic fragments by 4,4'-diisothiocyano dihydrostilbene-2,2'-disulfonate.阴离子跨红细胞膜转运、带3蛋白的原位蛋白水解以及4,4'-二异硫氰酸二氢芪-2,2'-二磺酸盐对蛋白水解片段的交联作用。
Biochim Biophys Acta. 1979 Jul 5;554(2):498-519. doi: 10.1016/0005-2736(79)90387-0.
3
The interaction of human erythrocyte Band 3 with cytoskeletal components.人类红细胞带3与细胞骨架成分的相互作用。
Arch Biochem Biophys. 1983 Nov;227(1):31-8. doi: 10.1016/0003-9861(83)90345-4.
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Alterations in pyridoxal 5'-phosphate inhibition of human erythrocyte anion transport associated with osmotic hemolysis and resealing.与渗透性溶血和重新封闭相关的5'-磷酸吡哆醛对人红细胞阴离子转运抑制作用的改变。
J Biol Chem. 1987 Nov 25;262(33):15974-8.
5
Effect of gossypol on erythrocyte membrane function: specific inhibition of inorganic anion exchange and interaction with band 3.棉酚对红细胞膜功能的影响:对无机阴离子交换的特异性抑制以及与带3蛋白的相互作用。
J Pharmacol Exp Ther. 1985 Sep;234(3):575-83.
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Intrinsic segments of band 3 that are associated with anion transport across red blood cell membranes.与阴离子跨红细胞膜转运相关的带3内在片段。
J Membr Biol. 1980 Dec 15;57(2):95-102. doi: 10.1007/BF01868996.
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Peptides of human erythrocyte band 3 protein produced by extracellular papain cleavage.细胞外木瓜蛋白酶切割产生的人红细胞带3蛋白的肽段。
J Biol Chem. 1984 Apr 10;259(7):4652-60.
8
Inhibition of anion transport associated with chymotryptic cleavages of red blood cell band 3 protein.抑制与红细胞带3蛋白胰凝乳蛋白酶裂解相关的阴离子转运。
Biochim Biophys Acta. 1981 Sep 7;646(3):471-8. doi: 10.1016/0005-2736(81)90317-5.
9
The location of a chymotrypsin cleavage site and of other sites in the primary structure of the 17,000-dalton transmembrane segment of band 3, the anion transport protein of red cell.红细胞阴离子转运蛋白带3的17000道尔顿跨膜片段一级结构中胰凝乳蛋白酶切割位点及其他位点的位置。
Membr Biochem. 1982;4(4):259-69. doi: 10.3109/09687688209065435.
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Erythrocyte band 3 protein: evidence for multiple membrane-crossing segments in the 17 000-dalton chymotryptic fragment.红细胞带3蛋白:17000道尔顿胰凝乳蛋白酶片段中多个跨膜区段的证据。
Biochemistry. 1984 Dec 18;23(26):6432-6. doi: 10.1021/bi00321a024.

引用本文的文献

1
Cell physiology and molecular mechanism of anion transport by erythrocyte band 3/AE1.红细胞带 3/AE1 转运阴离子的细胞生理学和分子机制。
Am J Physiol Cell Physiol. 2021 Dec 1;321(6):C1028-C1059. doi: 10.1152/ajpcell.00275.2021. Epub 2021 Oct 20.
2
Transport domain of the erythrocyte anion exchange protein.红细胞阴离子交换蛋白的转运结构域。
J Membr Biol. 1990 May;115(3):217-28. doi: 10.1007/BF01868637.