Structural models of carnitine acyltransferases and uses thereof
OwnerLiang Tong, Gerwald Joglinventors
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Abstract
The present invention relates to structural models of carnitine acyltransferases, and, in particular, to models of the reactive sites of these enzymes. It is based, at least in part, on the X-ray crystallographic structures of murine carnitine acetyltransferase (“mCRAT”), both in pure form and in complex with its substrates carnitine and coenzyme A (“CoA”). The structural information provides a basis for designing modulators of the activity of CRAT and related enzymes.
Claims45
Atomic coordinates for murine carnitine acetyltransferase, as set forth in FIG. 7, or coordinates having a root mean square deviation (RMSD) therefrom, with respect to at least 50% of Cα atoms, of not more than 4.0 Å, in computer readable form.
Atomic coordinates for human carnitine acetyltransferase, as set forth in FIG. 10, or coordinates having a RMSD therefrom, with respect to at least 50% of Cα atoms, of not more than 4.0 Å, in computer readable form.
Atomic coordinates for murine carnitine acetyltransferase bound to carnitine, as set forth in FIG. 8, or coordinates having a RMSD therefrom, with respect to at least 50% of Cα atoms, of not more than 4.0 Å, in computer readable form.
Atomic coordinates for murine carnitine acetyltransferase bound to coenzyme A, as set forth in FIG. 9, or coordinates having a RMSD therefrom, with respect to at least 50% of Cα atoms, of not more than 4.0 Å, in computer readable form.
A virtual model of the reactive site of murine carnitine acetyltransferase.
A computer displaying the virtual model of the reactive site of murine carnitine acetyltransferase.
A virtual model of the reactive site of human carnitine acetyltransferase.
A computer displaying the virtual model of the reactive site of human carnitine acetyltransferase.
A method for rationally designing a modulator of a carnitine acyltransferase, comprising, the steps of (i) producing a computer readable model of a molecule comprising a carnitine acyltransferase reactive site;
- and (ii) using the model to design a test compound having a structure and a charge distribution compatable with the reactive site, wherein the test compound comprises a functional group that may interact with the reactive site to modulate carnitine acyltransferase activity. They wanted to know whether we could claim a method for carnitine acetyltransferase for CPT activity.
A method of screening a plurality of test compounds, as represented in computer readable form, to identify a modulator of a carnitine acyltransferase, comprising the steps of (i) producing a computer readable model of a molecule comprising a carnitine acyltransferase reactive site;
- and (ii) using the model to identify, from among the test compounds, a modulator compound having a structure and a charge distribution compatable with the reactive site and comprising a functional group that may interact with the reactive site to modulate carnitine acyltransferase activity.
A method for rationally designing a compound for the treatment of diabetes, comprising the steps of (i) producing a computer readable model of a molecule comprising a carnitine acyltransferase reactive site;
- and (ii) using the model to design a test compound having a structure and a charge distribution compatable with the reactive site, wherein the test compound comprises a functional group that may interact with the reactive site to modulate carnitine acyltransferase activity;
- and (iii) evaluating the effects of the test compound in vivo, wherein an effect selected from the group consisting of a decrease in the acetyl-CoA/CoA ratio;
- a decrease in an intermediate or product of fatty acid oxidation;
- an increase in an intermediate or product of the Embden-Meyerhoff pathway;
- an increase in an intermediate or product of fatty acid synthesis;
- an increase in glycogen;
- and increased insulin sensitivity is an indicator of effectiveness of the test compound.
A method of screening a plurality of test compounds, as represented in computer readable form, to identify a compound useful for the treatment of diabetes, comprising the steps of (i) producing a computer readable model of a molecule comprising a carnitine acyltransferase reactive site;
- (ii) using the model to identify, from among the test compounds, a modulator compound having a structure and a charge distribution compatable with the reactive site and comprising a functional group that may interact with the reactive site to modulate carnitine acyltransferase activity;
- and (iii) evaluating the effects of the modulator compound in vivo, wherein an effect selected from the group consisting of a decrease in the acetyl-CoA/CoA ratio;
- a decrease in an intermediate or product of fatty acid oxidation;
- an increase in an intermediate or product of the Embden-Meyerhoff pathway;
- an increase in an intermediate or product of fatty acid synthesis;
- an increase in glycogen;
- and increased insulin sensitivity is an indicator of effectiveness of the modulator compound.
A set of atomic coordinates, as set forth in FIG. 7, or with coordinates having a RMSD therefrom, with respect to at least 50% of Cα atoms, of not more than 2.0 Å, wherein said coordinates define a three dimensional structure of crystalline mammalian CRAT.
A set of atomic coordinates, as set forth in FIG. 10, or with coordinates having a RMSD therefrom, with respect to at least 50% of Cα atoms, of not more than 2.0 Å, wherein said coordinates define a three dimensional structure of crystalline mammalian CRAT.
A crystalline form of mammalian CRAT, wherein the crystalline form of the mammalian CRAT is capable of being used for X-ray crystallographic studies, and wherein the crystalline form of the mammalian CRAT has a crystal structure with atomic structural coordinates as set forth in FIG. 7, or with coordinates having a RMSD therefrom, with respect to at least 50% of Cα atoms, of not more than 4.0 Å.
Dependencies are inferred from the claim text.