Laboratory of Peptide and Protein Chemistry, Centro de Investigación Príncipe Felipe, E-46012 Valencia, Spain.
J Biol Chem. 2011 Dec 30;286(52):44457-66. doi: 10.1074/jbc.M111.255364. Epub 2011 Nov 7.
The caspase recruitment domain (CARD) is present in a large number of proteins. Initially, the CARD was recognized as part of the caspase activation machinery. CARD-CARD interactions play a role in apoptosis and are responsible for the Apaf-1-mediated activation of procaspase-9 in the apoptosome. CARD-containing proteins mediate the inflammasome-dependent activation of proinflammatory caspase-1. More recently, new roles for CARD-containing proteins have been reported in signaling pathways associated with immune responses. The functional role of CARD-containing proteins and CARDs in coordinating apoptosis and inflammatory and immune responses is not completely understood. We have explored the putative cross-talk between apoptosis and inflammation by analyzing the modulatory activity on both the Apaf-1/procaspase-9 interaction and the inflammasome-mediated procaspase-1 activation of CARD-derived polypeptides. To this end, we analyzed the activity of individual recombinant CARDs, rationally designed CARD-derived peptides, and peptides derived from phage display.
半胱氨酸天冬氨酸蛋白酶募集结构域(CARD)存在于大量蛋白质中。最初,CARD 被认为是半胱氨酸天冬氨酸蛋白酶激活机制的一部分。CARD-CARD 相互作用在细胞凋亡中起作用,并负责衔接蛋白(Apaf-1)介导的前胱冬蛋白酶-9 在凋亡小体中的激活。含 CARD 的蛋白质介导炎症小体依赖性前炎症性胱冬蛋白酶-1 的激活。最近,在与免疫反应相关的信号通路中,报道了含 CARD 的蛋白质和 CARD 的新作用。含 CARD 的蛋白质和 CARD 在协调细胞凋亡和炎症及免疫反应中的功能作用尚未完全理解。我们通过分析对 Apaf-1/前胱冬蛋白酶-9 相互作用和炎症小体介导的前胱冬蛋白酶-1 激活的调节活性,探索了细胞凋亡和炎症之间的潜在串扰。为此,我们分析了单个重组 CARD、合理设计的 CARD 衍生肽以及噬菌体展示衍生肽的活性。