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从绿侧褶蛙皮肤分泌物中分离并鉴定一种新型缓激肽增强肽(BPP)

Isolation and characterization of a novel bradykinin potentiating peptide (BPP) from the skin secretion of Phyllomedusa hypochondrialis.

作者信息

Conceição Katia, Konno Katsuhiro, de Melo Robson Lopes, Antoniazzi Marta M, Jared Carlos, Sciani Juliana M, Conceição Isaltino M, Prezoto Benedito C, de Camargo Antônio Carlos Martins, Pimenta Daniel C

机构信息

Laboratório Especial de Toxinologia Aplicada, Center for Applied Toxinology (CAT/CEPID), Instituto Butantan, Avenida Vital Brasil 1500, São Paulo, SP 05503-900, Brazil.

出版信息

Peptides. 2007 Mar;28(3):515-23. doi: 10.1016/j.peptides.2006.10.002. Epub 2006 Nov 13.

Abstract

Bradykinin potentiating peptides (BPPs) from Bothrops jararaca venom were first described in the middle of 1960s and were the first natural inhibitors of the angiotensin-converting enzyme (ACE). BPPs present a classical motif and can be recognized by their typical pyroglutamyl (Pyr)/proline rich sequences presenting, invariably, a proline residue at the C-terminus. In the present study, we describe the isolation and biological characterization of a novel BPP isolated from the skin secretion of the Brazilian tree-frog Phyllomedusa hypochondrialis. This new BPP, named Phypo Xa presents the sequence Pyr-Phe-Arg-Pro-Ser-Tyr-Gln-Ile-Pro-Pro and is able to potentiate bradykinin activities in vivo and in vitro, as well as efficiently and competitively inhibit ACE. This is the first canonical BPP (i.e. Pyr-Aaa(n)-Gln-Ile-Pro-Pro) to be found not only in the frog skin but also in any other natural source other than the snake venoms.

摘要

来自巴西矛头蝮蛇毒液的缓激肽增强肽(BPPs)于20世纪60年代中期首次被描述,是最早的血管紧张素转换酶(ACE)天然抑制剂。BPPs具有一个经典基序,可通过其典型的焦谷氨酰(Pyr)/富含脯氨酸的序列识别,在C末端总是存在一个脯氨酸残基。在本研究中,我们描述了从巴西树蛙(Phyllomedusa hypochondrialis)皮肤分泌物中分离出的一种新型BPP的分离及生物学特性。这种新的BPP名为Phypo Xa,其序列为Pyr-Phe-Arg-Pro-Ser-Tyr-Gln-Ile-Pro-Pro,能够在体内和体外增强缓激肽活性,以及有效且竞争性地抑制ACE。这是首次在青蛙皮肤中发现,也是在蛇毒以外的任何其他天然来源中发现的首个典型BPP(即Pyr-Aaa(n)-Gln-Ile-Pro-Pro)。

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