Methods for screening proteins using DNA encoded chemical libraries as templates for enzyme catalysis
Disclosed are methods, compositions and devices for screening a protein library for proteins having a desired activity, such as capable of catalyzing the formation of a bond between two reactants. In an exemplary embodiments, a plurality of proteins are expressed in vitro from a plurality of nucleic acids, the plurality of proteins are exposed with two single stranded oligonucleotides having complementary sequences, each oligonucleotide having a reactant and a fluorophore, the fluorescence of the protein-reactant-oligonucleotide-fluorophore complexes is detected and the complexes showing detectable fluorescence energy transfer are isolated, thereby isolating proteins having the desired enzymatic activity.
1. A method for screening a protein library for a protein having a desired activity, the method comprising:
a) providing, at distinct features of a solid support, a plurality of nucleic acids, each nucleic acid having a predefined sequence;
b) expressing in vitro a plurality of proteins from the plurality of nucleic acids;
c) exposing the plurality of proteins to a first and a second oligonucleotide each, at one end, having a first and a second reactant, respectively, wherein a protein having a desired activity binds to the first and second reactants, thereby forming a complex; and
d) ligating free ends of the first and second oligonucleotides complexed with the protein having the desired activity.
2. The method of claim 1 wherein the first and second oligonucleotides are double-stranded oligonucleotides.
3. The method of claim 1 wherein the first and second oligonucleotides are single-stranded oligonucleotides.
4. The method of claim 3 further comprising adding a helper oligonucleotide capable of bridging the single-stranded oligonucleotides bound to the protein having the desired activity.
5. The method of claim 1 wherein each distinct feature is a well of a micro well plate.