Adhesiomics - Testing Protein-Protein Interaction of Cell Adhesion Proteins on Microarrays

C. Zeilinger
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Abstract

Protein microarray technology was used recently for targetoriented screening of chemically synthesized compound libraries or isolated natural compounds on Heat-Shock Proteins (Hsp), since Hsps together with the accompanied stress proteome are relevant targets in cancer and pathogenic organism [1-9]. An extended application of this method showed recently that the microarray technology enables also studies of protein-protein interaction to enable a broader application range [4,7]. The basic prerequisite for the formation of multicellular organisms is the ability of a single cell to communicate with neighboring cells. Molecules responsible for this intercellular communication are adhesion molecules like IgCAMs or gap junctions. The adhesion molecules represent a member of the immunoglobulin superfamily of Cell Adhesion Molecules (Ig-CAM). The protein has an extracellular domain, a transmembrane domain, as well as a highly conserved cytoplasmic tail.
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粘附组学-在微阵列上测试细胞粘附蛋白的蛋白质-蛋白质相互作用
蛋白微阵列技术最近被用于热休克蛋白(Heat-Shock Proteins, Hsp)上化学合成的化合物文库或分离的天然化合物的靶向筛选,因为热休克蛋白及其伴随的应激蛋白质组是癌症和致病性生物的相关靶标[1-9]。该方法的扩展应用最近表明,微阵列技术还可以研究蛋白质-蛋白质相互作用,从而实现更广泛的应用范围[4,7]。多细胞生物形成的基本先决条件是单个细胞与邻近细胞交流的能力。负责这种细胞间通讯的分子是粘附分子,如igcam或间隙连接。粘附分子是细胞粘附分子(Ig-CAM)免疫球蛋白超家族的一员。该蛋白具有胞外结构域、跨膜结构域以及高度保守的细胞质尾部。
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