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人血浆激肽原中的一种新的激肽部分。

A new kinin moiety in human plasma kininogens.

作者信息

Mindroiu T, Carretero O A, Proud D, Walz D, Scicli A G

机构信息

Hypertension Research Division, Henry Ford Hospital, Detroit, MI.

出版信息

Biochem Biophys Res Commun. 1988 Apr 29;152(2):519-26. doi: 10.1016/s0006-291x(88)80068-8.

DOI:10.1016/s0006-291x(88)80068-8
PMID:3365237
Abstract

Recently, we isolated a new kinin from human urine and tentatively identified it as [Ala3]-Lys-bradykinin. However, there were inconsistencies between the properties of the naturally occurring new kinin and synthetic [Ala3]-Lys-bradykinin. In the present work, we determined whether the new kinin was released from human plasma kininogen, and further investigated the structure of the new kinin. After incubation of plasma (n = 6) with human urinary kallikrein, kinins were separated by HPLC and measured by RIA. The new kinin and Lys-bradykinin were found representing 23 +/- 3 and 76 +/- 6%, respectively, of total kinins released (2.0 +/- 0.4 micrograms/ml). The new kinin was also released from both purified low- and high-molecular-weight kininogens, representing 40-42% of total kinins released. Amino acid sequencing and composition analysis indicated that the structure of the new kinin was [Hyp3]-Lys-bradykinin (Lys-Arg-Pro-Hyp-Gly-Phe-Ser-Pro-Phe-Arg) and not [Ala3]-Lys-bradykinin. We conclude that an important proportion of human kininogens contain hydroxyproline instead of proline in position three of the bradykinin moiety.

摘要

最近,我们从人尿中分离出一种新的激肽,并初步鉴定为[丙氨酸3]-赖氨酸-缓激肽。然而,天然存在的新激肽与合成的[丙氨酸3]-赖氨酸-缓激肽的性质之间存在不一致。在本研究中,我们确定了这种新激肽是否从人血浆激肽原中释放出来,并进一步研究了新激肽的结构。将血浆(n = 6)与人尿激肽释放酶孵育后,通过高效液相色谱法分离激肽,并通过放射免疫分析法进行测定。发现新激肽和赖氨酸-缓激肽分别占释放的总激肽的23±3%和76±6%(2.0±0.4微克/毫升)。新激肽也从纯化的低分子量和高分子量激肽原中释放出来,占释放的总激肽的40 - 42%。氨基酸测序和组成分析表明,新激肽的结构是[羟脯氨酸3]-赖氨酸-缓激肽(赖氨酸-精氨酸-脯氨酸-羟脯氨酸-甘氨酸-苯丙氨酸-丝氨酸-脯氨酸-苯丙氨酸-精氨酸),而不是[丙氨酸3]-赖氨酸-缓激肽。我们得出结论,相当一部分人激肽原在缓激肽部分的第三位含有羟脯氨酸而非脯氨酸。

相似文献

1
A new kinin moiety in human plasma kininogens.人血浆激肽原中的一种新的激肽部分。
Biochem Biophys Res Commun. 1988 Apr 29;152(2):519-26. doi: 10.1016/s0006-291x(88)80068-8.
2
Identification of a new kinin in human urine.人尿中一种新激肽的鉴定。
J Biol Chem. 1986 Jun 5;261(16):7407-11.
3
Identification of [hydroxyproline3]-lysyl-bradykinin released from human kininogens by human urinary kallikrein.人尿激肽释放酶从人激肽原释放的[羟脯氨酸3]-赖氨酰缓激肽的鉴定。
FEBS Lett. 1988 May 23;232(2):395-8. doi: 10.1016/0014-5793(88)80778-6.
4
Identification of [hydroxyproline3]-lysyl-bradykinin released from human plasma protein by kallikrein.激肽释放酶从人血浆蛋白中释放出的[羟脯氨酸3]-赖氨酰缓激肽的鉴定。
Biochem Biophys Res Commun. 1988 Jan 15;150(1):511-6. doi: 10.1016/0006-291x(88)90550-5.
5
Demonstration of arginyl-bradykinin moiety in rat HMW kininogen: direct evidence for liberation of bradykinin by rat glandular kallikreins.大鼠高分子量激肽原中精氨酰缓激肽部分的证实:大鼠腺体激肽释放酶释放缓激肽的直接证据。
Biochem Biophys Res Commun. 1985 Feb 28;127(1):289-95. doi: 10.1016/s0006-291x(85)80157-1.
6
Isolation of [hydroxyproline3]Lysyl-bradykinin formed by kallikrein from human plasma protein.从人血浆蛋白中分离激肽释放酶形成的[羟脯氨酸3]赖氨酰缓激肽。
Adv Exp Med Biol. 1989;247A:539-44. doi: 10.1007/978-1-4615-9543-4_83.
7
Inhibition of human and rat tissue kallikreins by peptide analog antagonists of bradykinin.
Adv Exp Med Biol. 1989;247B:277-81. doi: 10.1007/978-1-4615-9546-5_46.
8
Isolation and properties of two rat plasma T-kininogens.
Adv Exp Med Biol. 1986;198 Pt A:69-75. doi: 10.1007/978-1-4684-5143-6_10.
9
Ornitho-kininogen and ornitho-kinin: isolation, characterization and chemical structure.
Adv Exp Med Biol. 1989;247A:359-67. doi: 10.1007/978-1-4615-9543-4_54.
10
Release of [hydroxyproline3]-kinins by tissue kallikreins of pig, rat and man.猪、大鼠和人组织激肽释放酶释放[羟脯氨酸3]-激肽
Biochem Pharmacol. 1990 Feb 1;39(3):549-53. doi: 10.1016/0006-2952(90)90062-p.

引用本文的文献

1
Degradation pathway of kinins in tumor ascites and inhibition by kininase inhibitors: analysis by HPLC.肿瘤腹水中激肽的降解途径及激肽酶抑制剂的抑制作用:高效液相色谱分析
Agents Actions. 1990 Mar;29(3-4):172-80. doi: 10.1007/BF01966443.
2
Structure-activity studies on bradykinin and related peptides: agonists.缓激肽及相关肽的构效关系研究:激动剂
Br J Pharmacol. 1990 Mar;99(3):445-8. doi: 10.1111/j.1476-5381.1990.tb12947.x.