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, wherein the polypeptide is a sugar-binding protein or a kinase, 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) exerting a force of about 1 to about 10 pN on the polypeptide by hybridizing the single stranded polynucleotide to a complementary polynucleotide to alter the mechanical tension on the polypeptide, wherein the alteration of mechanical tension on the polypeptide effects an alteration of (i) the binding affinity for a kinase substrate, (ii) the binding affinity for a sugar, or (iii) the catalytic rate of the kinase, thereby altering the conformation of the polypeptide.
2. The method of claim 1 , wherein the polynucleotide comprises DNA or RNA.
3. The method of claim 1 , wherein the single stranded polynucleotide is from about 10 to about 100 bases in length.
4. The method of claim 1 , wherein the alteration of the conformation of the polypeptide lowers the binding affinity of the polypeptide for a kinase substrate bound by the polypeptide.
5. The method of claim 1 , wherein the alteration of the conformation of the polypeptide increases the binding affinity of the polypeptide for a kinase substrate bound by the polypeptide.
6. The method of claim 1 , wherein the alteration of the mechanical tension on the polypeptide is reversibly controlled by varying access of the polypeptide to the complementary polynucleotide.
7. A composition comprising a polypeptide coupled to a synthetic single stranded polynucleotide, wherein the polypeptide is a sugar-binding protein or a kinase, 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, and wherein the single stranded polynucleotide is selected so that:
(a) upon hybridization with a complementary polynucleotide, the polynucleotide coupled to the polypeptide 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 (i) the binding affinity for a kinase substrate, (ii) the binding affinity for a sugar, or (iii) the catalytic rate of the kinase.
8. The composition of claim 7 , wherein the polypeptide is a kinase and the alteration of the mechanical tension on the kinase effects an alteration of the catalytic rate of the kinase.
9. The composition of claim 7 , wherein the alteration of the binding affinity and/or catalytic rate effects production of a detectable signal.
10. The composition of claim 9 , wherein the detectable signal is mediated by a fluorescent agent, a chemiluminescent agent or a chromophore.
11. A method of detecting the presence of a target molecule in a sample comprising:
(a) contacting the sample with the composition of claim 9 ; and
(b) detecting the presence of a detectable signal, whereby the presence of a detectable signal is indicative of the presence of the target molecule,
wherein the target molecule is a polynucleotide which is complementary to the single stranded polynucleotide coupled to the polypeptide of the composition of claim 9 , wherein hybridization of the target molecule to the single stranded polynucleotide results in an alteration of mechanical tension on the polypeptide of about 1 to about 10 pN, wherein the alteration of mechanical tension on the polypeptide effects an alteration of (i) the binding affinity for a kinase substrate, (ii) the binding affinity for a sugar, or (iii) the catalytic rate of the kinase, and wherein the alteration of the binding affinity and/or the catalytic rate results in the production of a detectable signal.
12. The composition of claim 7 , wherein the polypeptide is a kinase.
13. The composition of claim 12 , wherein the kinase is guanylate kinase or protein kinase A.
14. The composition of claim 7 , wherein the polypeptide is a sugar-binding protein.
15. The composition of claim 14 , wherein the sugar-binding protein is maltose binding protein.
16. The composition of claim 7 , wherein the single stranded polynucleotide is about 10 to about 100 bases in length.
17. The composition of claim 7 , wherein the single stranded polynucleotide is about 20 to about 80 bases in length.