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    • 10. 发明授权
    • Mass spectrometric methods for biomolecular screening
    • 用于生物分子筛选的质谱法
    • US06329146B1
    • 2001-12-11
    • US09260310
    • 1999-03-02
    • Stanley T. CrookeRichard GriffeySteven Hofstadler
    • Stanley T. CrookeRichard GriffeySteven Hofstadler
    • C12Q168
    • C12Q1/6816B01J2219/00702B01J2219/00722C12Q1/6806C12Q1/6811C40B40/06H01J49/004Y10T436/24C12Q2565/627C12Q2525/101C12Q2565/133C12Q2525/121C12Q2565/607
    • The present invention provides methods for the determination of the structure of biomolecular targets, as well as the site and nature of the interaction between ligands and biomolecular targets. The present invention also provides methods for the determination of the relative affinity of a ligand for the biomolecular target it interacts with. Also provided are methods for screening ligand or combinatorial libraries of compounds against one or more than one biological target molecules. The methods of the invention also allow determination of the relative binding affinity of combinatorial and other compounds for a biomolecular target. The present invention further provides methods for the use of mass modifying tags for screening multiple biomolecular targets. In a preferred embodiment, ligands which have great specificity and affinity for molecular interaction sites on biomolecules, especially RNA can be identified. In preferred embodiments, such identification can be made simultaneously with libraries of ligands.
    • 本发明提供了用于确定生物分子靶标的结构的方法,以及配体和生物分子靶标之间的相互作用的位点和性质。 本发明还提供了确定配体与其相互作用的生物分子靶的相对亲和力的方法。 还提供了用于筛选针对一种或多于一种生物靶分子的化合物的配体或组合文库的方法。 本发明的方法还允许确定组合和其它化合物对于生物分子靶标的相对结合亲和力。 本发明还提供使用质量修饰标签筛选多个生物分子靶标的方法。 在优选的实施方案中,可以鉴定对生物分子,特别是RNA上的分子相互作用位点具有极大特异性和亲和力的配体。 在优选的实施方案中,这种鉴定可以与配体文库同时进行。