组合化学与大规模筛选相结合用于识别与治疗用靶蛋白结合的化合物即潜在新药。
Combinatorial chemistry is used in tandem with high-throughput screening to identify compounds that bind to a therapeutic target protein and are thus potential new drugs.
发现,麦胶蛋白的浓度影响单宁酸与麦胶蛋白结合的方式,也影响二者的结合比例。
It was found that the con-centration influences the mode and the ratio of complexation of tannic acid with gliadin.
这些分子结合在一起,在蛋白质中形成所谓的希夫碱。
The molecules combine, forming what is called a Schiff base within the protein.
When the ligand is present it binds to the receptor outside the cell and it activates this G-protein.
当配体存在并与细胞表面的受体结合时,就会激活G蛋白
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