Allosteric control of proteins by manipulating mechanical tension
View Patent ↗A method of altering the conformation of a polypeptide having a known three-dimensional structure is described. The method comprises attaching a first end of a polymer to a first portion of the polypeptide, attaching a second end of the polymer to a second portion of the polypeptide, and altering the mechanical tension of the polymer, thereby altering the conformation of the polypeptide. The alteration of the conformation of the polypeptide may increase or decrease the binding affinity of the polypeptide for a substrate bound by the polypeptide, or alter the catalytic rate of an enzyme. Typically, the polymer is a polynucleotide or polypeptide.
1. A method of altering the conformation of a polypeptide having a known three-dimensional structure, wherein the polypeptide comprises two domains and a binding cleft between the two domains, or an enzyme, the method comprising:
(a) covalently attaching a first end of a synthetic single stranded polynucleotide to a first portion of the polypeptide;
(b) covalently attaching a second end of the single stranded polynucleotide to a second portion of the polypeptide; and
(c) altering the mechanical tension of the single stranded polynucleotide by hybridizing the single stranded polynucleotide to a complementary polynucleotide;
thereby altering the conformation of the polypeptide.
2. The method of claim 1 , wherein the polynucleotide is DNA, or RNA.
3. The method of claim 1 , wherein the polynucleotide is from about 10 to about 100 bases in length.
4. The method of claim 1 , wherein the polypeptide is a kinase or a sugar-binding protein and the alteration of the conformation of the polypeptide lowers the binding affinity of the polypeptide for a substrate or other molecule bound by the polypeptide relative to the binding affinity for the substrate or other molecule prior to the alteration of the conformation of the polypeptide.
5. The method of claim 1 , wherein the polypeptide is a kinase or a sugar-binding protein and the alteration of the conformation of the polypeptide increases the binding affinity of the polypeptide for a substrate or other molecule bound by the polypeptide relative to the binding affinity for the substrate or other molecule prior to the alteration of the conformation of the polypeptide.
6. The method of claim 1 , wherein the alteration of the mechanical tension of the polypeptide is reversibly controlled by varying access of the polypeptide to the single stranded polynucleotide.
7. A composition comprising a polypeptide coupled to a synthetic single stranded polynucleotide, wherein a first end of the polynucleotide is covalently attached to a first portion of the polypeptide and a second end of the polynucleotide is covalently attached to a second portion of the polypeptide, wherein the polypeptide comprises (i) a sugar-binding protein comprising two domains and a binding cleft between the two domains, or (ii) a kinase, and wherein the single stranded polynucleotide is selected so that:
(a) upon contact with a chemical signal, the polynucleotide exerts an alteration of mechanical tension on the polypeptide of about 1 to about 10 pN; and
(b) the alteration of mechanical tension on the polypeptide effects an alteration of the binding affinity for a substrate or other molecule bound by the polypeptide and/or catalytic rate of the polypeptide.
8. The composition of claim 7 , wherein the chemical signal is a complementary polynucleotide.
9. The composition of claim 7 , wherein the polypeptide is a kinase.
10. The composition of claim 9 , wherein the alteration of the mechanical tension on the enzyme effects an alteration of the catalytic rate of the kinase.
11. The composition of claim 7 , wherein the alteration of the binding affinity for a substrate or other molecule bound by the polypeptide and/or catalytic rate effects production of a detectable signal.
12. The composition of claim 11 , wherein the detectable signal is mediated by a fluorescent agent, a chemiluminescent agent or a chromophore.
13. A method of detecting the presence of a target molecule in a sample comprising:
(a) contacting the sample with a composition according to claim 11 , wherein the target molecule is the chemical signal; and
(b) detecting the presence of the detectable signal, whereby presence of the detectable signal is indicative of the presence of the target molecule.
14. The method of claim 1 , wherein the polypeptide comprises an enzyme.
15. The method of claim 14 , wherein the enzyme catalyzes a reaction leading to the production of a fluorescent or chemo-luminescent molecule, or a chromophore.
16. The method of claim 14 , wherein the enzyme is a kinase.
17. The method of claim 1 , wherein the polypeptide comprises two domains and a binding cleft between the two domains.