即使我们能抓住蛋白质折叠的规律，下一步就是通过分析数百万蛋白质和其它分子之间的相互作用，来预测细胞的结构。
Even if we could solve protein-folding, the next stage would be to predict the structure of cells on the basis of the interactions of millions of proteins and other molecules.
这些实验为解答T细胞迁移及与肿瘤细胞相互作用的分子条件提供了基础。
These experiments set the basis for unraveling the molecular requirements for t cell migration and t cell-tumor cell interactions.
G -蛋白偶联受体分布于细胞膜，与行使细胞通讯的分子(如神经递质和激素)发生相互作用。
Found in the cell membrane, GPCRs interact with molecules responsible for cellular communication such as neurotransmitters and hormones.
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