发明名称 Molecular switches and methods for making and using the same
摘要 The invention provides molecular switches which couple external signals to functionality and to methods of making and using the same. The switches according to the invention can be used, for example, to regulate gene transcription, target drug delivery to specific cells, transport drugs intracellularly, control drug release, provide conditionally active proteins, perform metabolic engineering, and modulate cell signaling pathways. Libraries comprising the switches and expression vectors and host cells for expressing the switches are also provided.
申请公布号 US9273319(B2) 申请公布日期 2016.03.01
申请号 US201313779788 申请日期 2013.02.28
申请人 The Johns Hopkins University 发明人 Ostermeier Marc
分类号 A61K31/70;C12N15/64;C12N15/74;C07H21/04;C12N15/63;C12N15/10;C12N15/62;A61K48/00 主分类号 A61K31/70
代理机构 Johns Hopkins Technology Transfer 代理人 Johns Hopkins Technology Transfer
主权项 1. A method for modulating a cellular activity in a cell or population of cells, comprising providing a fusion molecule to the cell or population of cells wherein the fusion molecule is encoded by a nucleic acid sequence and is generated according to the method comprising: a) creating an insertion nucleic acid sequence library in vitro comprising the steps of: i) obtaining an insertion nucleic acid sequence which encodes a polypeptide that recognizes a signal of interest;ii) ligating the insertion nucleic acid sequence under conditions sufficient to circularize the insertion nucleic acid sequence;iii) digesting the insertion nucleic acid sequence of ii) under conditions sufficient to randomly introduce a double-stranded break to create the insertion nucleic acid sequence library; b) creating an acceptor nucleic acid sequence library in vitro comprising the steps of: i) obtaining an acceptor nucleic acid sequence which encodes a polypeptide that produces a measurable change in a desired state, provided the measurable change in state is not fluorescence;ii) ligating the acceptor nucleic acid sequence under conditions sufficient to circularize an acceptor nucleic acid sequence;iii) digesting the acceptor nucleic acid sequence of ii) under conditions sufficient to randomly introduce a double-stranded break to create an acceptor nucleic acid sequence library; c) ligating the nucleic acids of the libraries of a) and b) in vitro under sufficient conditions such that an insertion nucleic acid sequence will randomly insert into the randomly introduced double strand break in an acceptor nucleic acid sequence, d) transforming a suitable host cell in vitro with the ligated libraries of c); e) selecting for a transformed host cell in vitro expressing the modulatable fusion polypeptide by exposing the transformed host cell to the signal of interest and identifying the transformed host cell which exhibits a measurable change of the desired state; f) isolating the nucleic acid sequence encoding the fusion molecule from the transformed host cell of e); g) cloning the nucleic acid sequence encoding the fusion molecule into a suitable expression vector; h) transferring the suitable expression vector of g) to the host cell or population of cells in vitro or in vivo; and exposing the cell or population of cells to the signal of interest and changing the state of the acceptor portion of the fusion molecule, thereby modulating the cellular activity of the cell or population of cells.
地址 Baltimore MD US