Suppr超能文献

BYC,一种来自微小扇头蜱(微小牛蜱)卵的非典型天冬氨酸内肽酶。

BYC, an atypical aspartic endopeptidase from Rhipicephalus (Boophilus) microplus eggs.

作者信息

Nascimento-Silva Maria Clara L, Leal Alexandre T, Daffre Sirlei, Juliano Luiz, da Silva Vaz Itabajara, Paiva-Silva Gabriela de O, Oliveira Pedro L, Sorgine Marcos Henrique F

机构信息

Instituto de Bioquímica Médica, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.

出版信息

Comp Biochem Physiol B Biochem Mol Biol. 2008 Apr;149(4):599-607. doi: 10.1016/j.cbpb.2007.12.007. Epub 2007 Dec 28.

Abstract

An aspartic endopeptidase was purified in our laboratory from Rhipicephalus (Boophilus) microplus eggs [Logullo, C., Vaz, I.S., Sorgine, M.H., Paiva-Silva, G.O., Faria, F.S., Zingali, R.B., De Lima, M.F., Abreu, L., Oliveira, E.F., Alves, E.W., Masuda, H., Gonzales, J.C., Masuda, A., and Oliveira, P.L., 1998. Isolation of an aspartic proteinase precursor from the egg of a hard tick, Rhipicephalus (Boophilus) microplus. Parasitology 116, 525-532]. Boophilus yolk cathepsin (BYC) was tested as component of a protective vaccine against the tick, inducing a significant immune response in cattle [da Silva, V.I., Jr., Logullo, C., Sorgine, M., Velloso, F.F., Rosa de Lima, M.F., Gonzales, J.C., Masuda, H., Oliveira, P.L., and Masuda, A., 1998. Immunization of bovines with an aspartic proteinase precursor isolated from Rhipicephalus (Boophilus) microplus eggs. Vet. Immunol. Immunopathol. 66, 331-341]. In this work, BYC was cloned and its primary sequence showed high similarity with other aspartic endopeptidases. In spite of this similarity, BYC sequence shows many important differences in relation to other aspartic peptidases, the most important being the lack of the second catalytic Asp residue, considered to be essential for the catalysis of this class of endopeptidases. When we determined BYC cleavage specificity by LC-MS, we found out that it presents a preference for hydrophobic residues in P1 and P1' in accordance to most aspartic endopeptidases. Also, when analyzed by circular dicroism, BYC presented high beta sheet content, also a characteristic of aspartic endopeptidases. On the other hand, although both native and recombinant BYC are catalytically active, they present a very low specific activity, what seems to indicate that this peptidase will digest its natural substrate, vitellin, very slowly. We speculate that such a slow Vn degradative process might constitute an important strategy to preserve egg protein content to the hatching larvae.

摘要

我们实验室从微小扇头蜱(Rhipicephalus (Boophilus) microplus)的卵中纯化出一种天冬氨酸内肽酶[洛古洛,C.,瓦斯,I.S.,索尔金,M.H.,派瓦 - 席尔瓦,G.O.,法里亚,F.S.,津加利,R.B.,德利马,M.F.,阿布雷乌,L.,奥利维拉,E.F.,阿尔维斯,E.W.,增田,H.,冈萨雷斯,J.C.,增田,A.,以及奥利维拉,P.L.,1998年。从硬蜱微小扇头蜱的卵中分离出一种天冬氨酸蛋白酶前体。《寄生虫学》116卷,525 - 532页]。已对扇头蜱卵组织蛋白酶(BYC)作为蜱的保护性疫苗成分进行了测试,它能在牛体内诱导显著的免疫反应[小达席尔瓦,V.I.,洛古洛,C.,索尔金,M.,维洛索,F.F.,罗莎·德利马,M.F.,冈萨雷斯,J.C.,增田,H.,奥利维拉,P.L.,以及增田,A.,1998年。用从微小扇头蜱卵中分离出的天冬氨酸蛋白酶前体免疫牛。《兽医免疫学与免疫病理学》66卷,331 - 341页]。在这项研究中,BYC被克隆,其一级序列与其他天冬氨酸内肽酶具有高度相似性。尽管存在这种相似性,但BYC序列与其他天冬氨酸肽酶相比仍有许多重要差异,其中最重要的是缺少第二个催化性天冬氨酸残基,而该残基被认为是这类内肽酶催化所必需的。当我们通过液相色谱 - 质谱法测定BYC的切割特异性时,发现它与大多数天冬氨酸内肽酶一样,对P1和P1'位的疏水性残基有偏好。此外,通过圆二色性分析发现,BYC具有较高的β折叠含量,这也是天冬氨酸内肽酶的一个特征。另一方面,尽管天然和重组的BYC都具有催化活性,但它们的比活性非常低,这似乎表明这种肽酶对其天然底物卵黄磷蛋白的消化非常缓慢。我们推测,如此缓慢的卵黄磷蛋白降解过程可能是一种将卵蛋白含量保留给孵化幼虫的重要策略。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验