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新型人基质金属蛋白酶-1(MMP-3)和基质金属蛋白酶-2(MMP-10)特异性鼠抗体制备用于生化和免疫组织化学分析。

Novel specific human and mouse stromelysin-1 (MMP-3) and stromelysin-2 (MMP-10) antibodies for biochemical and immunohistochemical analyses.

机构信息

Wound Repair Unit, Centre for Biomolecular Interactions Bremen, Department of Biology and Biochemistry, University of Bremen, Bremen, Germany.

Hannover Medical School, Institute for Laboratory Animal Science, Hannover, Germany.

出版信息

Wound Repair Regen. 2019 Jul;27(4):309-323. doi: 10.1111/wrr.12704. Epub 2019 Mar 7.

Abstract

Matrix metalloproteinases (MMP) are a family of more than 25 zinc-dependent enzymes that are centrally involved in cellular migration, tissue remodeling, cancer invasion and metastasis. Besides degrading extracellular matrix proteins, MMPs are crucial for growth factor and cytokine release and activation. At the same time, they can inactivate inflammatory mediators and enzymes themselves through protein degradation. Subclasses of MMPs include collagenases, gelatinases, stromelysins, membrane-bound MMPs, and others. With regard to the stromelysin subfamily, three members exist, e.g., stromelysin-1 (MMP-3), stromelysin-2 (MMP-10), and stromelysin-3 (MMP-11). MMP-3, and MMP-10 share extensive similarities at the amino acid level that made it difficult to develop specific antibodies distinguishing between MMP-3 and MMP-10. Scrutinizing published data on and performing different analyses with detection of both stromelysins with commercially available or lab-made antibodies showed ambiguous results with regard to specificity of antibodies used to date. We developed new specific antibodies against the most divergent parts of the active forms of both proteins. We assessed the specificity of our novel specific anti-human and anti-mouse MMP-3 and MMP-10 antibodies in cell lysates and different human and murine skin tissues. Tests analyzing specificity of the novel antibodies included Western immunoblotting, immunofluorescence, and immunohistochemistry on paraffin sections. Analyses demonstrated specific detection of respective protein for human or mouse samples except for the anti-human MMP-3 antibody. The aim of this summary was to call attention the MMP research community to distinguish clearly between both enzymes. Our new specific anti-mouse MMP-3 and both MMP-10 antibodies allow us to address this detection problem and to enable comparative studies between both stromelysins with regard to their respective location and function in the tissue.

摘要

基质金属蛋白酶(MMP)是一个锌依赖性酶家族,超过 25 种,它们主要参与细胞迁移、组织重塑、癌症侵袭和转移。除了降解细胞外基质蛋白外,MMP 对于生长因子和细胞因子的释放和激活也至关重要。同时,它们可以通过蛋白降解来失活炎症介质和自身的酶。MMP 的亚类包括胶原酶、明胶酶、基质溶解素、膜结合 MMP 等。就基质溶解素亚家族而言,存在三个成员,例如基质溶解素-1(MMP-3)、基质溶解素-2(MMP-10)和基质溶解素-3(MMP-11)。MMP-3 和 MMP-10 在氨基酸水平上有广泛的相似性,这使得很难开发出特异性抗体来区分 MMP-3 和 MMP-10。仔细审查已发表的数据,并使用商业上可用的或实验室制造的抗体对两种基质溶解素进行不同的分析,显示出迄今为止使用的抗体的特异性存在模糊的结果。我们针对这两种蛋白质的活性形式的最不同部分开发了新的特异性抗体。我们在细胞裂解物和不同的人和鼠皮肤组织中评估了我们新的特异性抗人 MMP-3 和 MMP-10 抗体的特异性。分析特异性的测试包括 Western 免疫印迹、免疫荧光和石蜡切片的免疫组织化学。分析表明,除了抗人 MMP-3 抗体外,针对人或鼠样本的特异性检测到各自的蛋白。本摘要的目的是引起 MMP 研究界的注意,以清楚地区分这两种酶。我们新的特异性抗鼠 MMP-3 和 MMP-10 抗体使我们能够解决这个检测问题,并能够在组织中对两种基质溶解素进行比较研究,以了解它们各自的位置和功能。

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