Aureli Loretta, Gioia Magda, Cerbara Ilaria, Monaco Susanna, Fasciglione Giovanni Francesco, Marini Stefano, Ascenzi Paolo, Topai Alessandra, Coletta Massimo
Colosseum Combinatorial Chemistry Centre for Technology (C4T S.C.a r.l.), Via della Ricerca Scientifica s.n.c, I-00133 Roma, Italy.
Curr Med Chem. 2008;15(22):2192-222. doi: 10.2174/092986708785747490.
Matrix metalloproteinases (MMPs) are a family of zinc-dependent endopeptidases which are involved in the proteolytic processing of several components of the extracellular matrix. As a consequence, MMPs are implicated in several physiological and pathological processes, like skeletal growth and remodelling, wound healing, cancer, arthritis, and multiple sclerosis, raising a very widespread interest toward this class of enzymes as potential therapeutic targets. Here, structure-function relationships are discussed to highlight the role of different MMP domains on substrate/inhibitor recognition and processing and to attempt the formulation of advanced guidelines, based on natural substrates, for the design of inhibitors more efficient in vivo.
基质金属蛋白酶(MMPs)是一类锌依赖性内肽酶,参与细胞外基质多种成分的蛋白水解过程。因此,MMPs与多种生理和病理过程相关,如骨骼生长与重塑、伤口愈合、癌症、关节炎和多发性硬化症,这引发了人们对这类酶作为潜在治疗靶点的广泛关注。本文讨论了结构-功能关系,以突出不同MMP结构域在底物/抑制剂识别与加工中的作用,并尝试基于天然底物制定先进的指导方针,用于设计在体内更有效的抑制剂。