为便于从融合蛋白中解离出目的多肽，这个载体中含有特异的蛋白酶裂解位点。
This vector also contains thrombin protease cleavage site to facilitate proteolysis of the bacterial fusion proteins.
通道表面的结合位点是动力学位点，药物更容易结合，同时也更容易解离。
Our study is the first computational work that provides both kinetic and thermodynamic energy information on these drug binding sites.
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