de Paula Fernando Fonseca Pereira, Ribeiro Juliana Uema, Santos Livia Mara, de Souza Dulce Helena Ferreira, Leonardecz Eduardo, Henrique-Silva Flávio, Selistre-de-Araújo Heloisa Sobreiro
Departamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos, SP, Brazil; Universidade de Brasília, Campus Planaltina - UnB/FUP Brazil, Brazil.
Departamento de Ciências Fisiológicas, Universidade Federal de São Carlos, São Carlos, SP, Brazil.
Comp Biochem Physiol Part D Genomics Proteomics. 2014 Dec;12:74-83. doi: 10.1016/j.cbd.2014.09.001. Epub 2014 Oct 27.
We have previously demonstrated that alternagin-C (ALT-C), a disintegrin-like, Cys-rich protein isolated from Bothrops alternatus snake venom, induces human vascular endothelial cell (HUVEC) proliferation and angiogenesis in in vitro and in vivo assays. Therefore this protein could be interesting as a new approach for tissue regeneration studies. However, its primary sequence was not completely determined since the protein isolated from crude venom is usually a mixture of isoforms. Here we describe the transcriptome analysis of B. alternatus from the venom glands of a single male specimen. About 800 good-quality contigs were screened for snake venom metalloproteases/disintegrins, resulting in the following expression profile for these enzymes: 4% for P-I, 7% for P-II and 89% for P-III SVMPs. The PII-SVMP sequence code for RGD-disintegrins and all the expressed PIII-sequences have the ECD adhesive motif. A cDNA sequence coding for an ALT-C homolog was completely sequenced and characterized. Comparative sequence and structural analyses suggested new features that distinguish SVMP classes such as two prolyl endopetidase cleavage sites. All these data add new information on the expression pattern of metalloproteases of B. alternatus venom and may have practical applications for the production of recombinant disintegrins for cell adhesion studies.
我们之前已经证明,从矛头蝮蛇毒中分离出的一种去整合素样、富含半胱氨酸的蛋白质——交替糖蛋白-C(ALT-C),在体外和体内试验中均可诱导人血管内皮细胞(HUVEC)增殖和血管生成。因此,这种蛋白质作为组织再生研究的一种新方法可能很有意义。然而,由于从粗毒液中分离出的蛋白质通常是多种异构体的混合物,其一级序列尚未完全确定。在此,我们描述了对单个雄性标本毒腺中的矛头蝮进行的转录组分析。针对蛇毒金属蛋白酶/去整合素筛选了约800个高质量重叠群,得出这些酶的以下表达谱:P-I型占4%,P-II型占7%,P-III型蛇毒金属蛋白酶占89%。PII型蛇毒金属蛋白酶序列编码RGD-去整合素,所有表达的PIII型序列都具有ECD粘附基序。编码ALT-C同源物的cDNA序列已被完全测序和表征。比较序列和结构分析揭示了区分蛇毒金属蛋白酶类别的新特征,如两个脯氨酰内肽酶切割位点。所有这些数据为矛头蝮蛇毒金属蛋白酶的表达模式增添了新信息,可能在生产用于细胞粘附研究的重组去整合素方面具有实际应用价值。