A yeast genetic system for selecting small molecule inhibitors of protein-protein interactions in nanodroplets

被引:109
作者
Huang, J [1 ]
Schreiber, SL [1 ]
机构
[1] HARVARD UNIV,HOWARD HUGHES MED INST,DEPT CHEM & BIOL CHEM,CAMBRIDGE,MA 02138
基金
澳大利亚研究理事会;
关键词
D O I
10.1073/pnas.94.25.13396
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cellular processes are mediated by complex networks of molecular interactions. Dissection of their role most: commonly is achieved by using genetic mutations that alter, for example, protein-protein interactions, Small molecules that accomplish the same result would provide a powerful camplement to the genetic approach, but it generally is believed that: such molecules are rare, There art several natural products, however, that illustrate the feasibility of this approach. Split-pool synthesis now provides a simple mechanical means to prepare vast numbers of complex, even natural product-like, molecules individually attached to cell-sized polymer beads. Here, we describe a genetic system compatible with split-pool synthesis that allows the detection of cell-permeable, small molecule inhibitors of protein-protein interactions in 100- to ZOO-nr cell culture droplets, prepared by a recently described technique that: arrays large numbers df such droplets. These ''nanodroplets'' contain defined media, cells, and. one or more beads containing approximate to 100 pmol of a photoreleasable small molecule and a controlled number of cells. The engineered Saccharomyces cerevisiae cells used in this study express two interacting proteins after induction with galactose whose interaction results in cell death in the presence of 5-fluoroorotic acid (inducible reverse two-hybrid assay). Disruption of the interaction by a small molecule allows growth, and the small molecule can be introduced into the system hours before induction of the toxic interaction, We demonstrate that the interaction between the activin receptor R1 and the immunophilin protein FKB12 can be disrupted by the small molecule FK506 at nanomolar concentrations in nanodroplets. This system should provide a general method for selecting cell-permeable ligands that can ire used to study the relevance of protein-protein interactions in living cells or organisms.
引用
收藏
页码:13396 / 13401
页数:6
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