US20100028895A1

US20100028895A1 - Method for determining the stability of organic methyleneamines in the presence of semicarbazide-sensitive amine oxidase

Info

Publication number: US20100028895A1
Application number: US12/518,318
Authority: US
Inventors: Adedayo Adedoyin; Michael Angelastro; Julie Bick; Jennifer Cairns; Yongqing Huang; Guyan Liang; Heng-Keang Lim
Original assignee: Sanofi Aventis France
Current assignee: Sanofi SA
Priority date: 2007-01-10
Filing date: 2008-01-08
Publication date: 2010-02-04
Also published as: HK1137784A1; IL199707A0; TW200907065A; NZ578079A; US20140363836A1; GT200900199A; CA2674704A1; WO2008086325A8; TN2009000232A1; CN101578375B; DOP2009000175A; JP2010515461A; MX2009005962A; ECSP099507A; HN2009001289A; CR10862A; JP2014204727A; US8883410B2; SG177920A1; UA103300C2

Abstract

The present invention provides methods for determining the stability of methyleneamine, methyleneamine-like compounds or compounds containing an methyleneamine moiety in the presence of semicarbazide-sensitive amine oxidase (SSAO) or a biological sample containing SSAO activity. The disclosed methods may be configured in an assay format for high throughput screening applications.

Description

BACKGROUND OF THE INVENTION

Semicarbazide-sensitive amine oxidases (SSAO) are widely distributed in tissues, particularly in blood vessels, suggesting a role for this enzyme for inactivating circulating methyleneamines (Lyles, Prog. Brain Res., 106:293-303, 1995). Many investigators have focused their efforts on finding an endogenous ligand for SSAO and on looking for inhibitors of this enzyme (Precious et al., Biochem. Pharmacol., 37:707-713, 1988; Crosbie and Callingham, J. Neural Transm. Suppl., 41:427-432, 1994; Elliot et al., Biochem. Pharmacol. 38:1507-1515, 1989; Boomsma et al., Comp. Biochem. Physiol. C Toxicol. Pharmacol., 126:69-78, 2000; Yraola et al., J. Med. Chem. 49:6197-6208; WO 02/066669). Others have searched for alternative physiological roles of SSAO. For example, SSAO, also called vascular adhesion protein-1 (VAP-1), has been shown to be up-regulated under inflammatory conditions and to mediate the binding of lymphocytes (WO 98/53049). The instant invention utilizes the enzyme activity of SSAO to measure the metabolic stability of test agents in cells and biological samples.
Metabolic stability of test agents has become a critical factor in drug development, thus, the instant invention solves the problem of identifying potential test agents that are subject to metabolism by SSAO. Advances in chemistry, molecular biology and high-throughput technology have provided drug discovery programs with the ability to screen an enormous number of compounds against a large number of targets to identify lead compounds. These leads then undergo more selection criteria to identify those compounds with optimal “drug-like” properties (i.e., adequate physico-chemical stability, solubility, safety, efficacy, in vivo disposition). Significant efforts are directed toward identifying and eliminating compounds (or compound classes) that are not likely to have “drug-like” properties at earlier stages of discovery. The three main reasons a drug fails during clinical trials are lack of efficacy, unacceptable adverse effects, and unfavorable ADME (absorption, distribution, metabolism, excretion) properties. Therefore the ultimate success of a compound is not only defined by its biological activity and potency, but also by its ADME/toxicity properties. As a result, lead optimization programs have incorporated screens to select drugs with desirable ADME/toxicity properties to enhance the likelihood that new lead compounds will have success in the clinic. Metabolic transformation of drug molecules represents a key process by which drugs are cleared from the body. Given the wide distribution of SSAO in many bodily compartments, we believe SSAO may be an important enzyme that contributes to a drug's potential metabolic liability. Thus, the instant invention uses methods of determining the metabolic stability of test agents exposed to SSAO. Methods directed to determining the metabolism of a drug or other test agent by enzymes involved in biotransformation, in particular SSAO, have important implications for drug development.
In in vitro studies, compound A (U.S. Pat. No. 6,977,263 B) was incubated with plasma of various species including human. Compound A was observed to be more stable in human plasma in comparison to sheep, guinea pig, rat, and mouse up to one hour. Additionally, no significant metabolism or degradation was observed for the compound in human plasma up to 4 hours with or without semicarbazide. However, pharmacokinetic data from the “first in man” study showed that the same compound was rapidly metabolized and to a far greater extent than that demonstrated in vitro using plasma from human and from other species. Subsequent studies confirmed that membrane-bound SSAO was primarily responsible for the metabolism of the compound in man. These data indicate that soluble SSAO found in human plasma does not possess the same level of enzyme activity and/or substrate specificity as the membrane bound SSAO under physiological conditions. Therefore, as illustrated by compound A, measuring human plasma stability is not predictive of SSAO stability in man and thus is of limited utility in selecting pharmaceutical agents as clinical candidates.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows the amino acid sequence of human SSAO (Genbank Accession No. Q16853; SEQ ID NO: 1).

FIG. 2 shows the nucleotide sequence of human SSAO (Genbank Accession No. NM_—00374; SEQ ID NO: 2).

FIG. 3 shows the chemical structure of compound A.

DETAILED DESCRIPTION OF THE INVENTION

All publications cited herein are hereby incorporated by reference. Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood to one of ordinary skill in the art to which this invention pertains.
The terminology used in this specification and the appended claims is for the purpose of describing particular embodiments only and the use in the specification is not intended to be limiting of the invention. The singular forms of a word are intended to include the plural forms unless the context clearly indicates otherwise. For example, the singular forms of “a”, “an” and “the” are intended to include the plural forms as well. Further, reference to an agent may include a mixture of two or more agents. Thus, the term “an agent” includes a plurality of agents, including mixtures and/or enantiomers thereof. It should also be noted that the term “or” is generally employed in its sense including “and/or” unless the content clearly dictates otherwise. It will be further understood that the terms “comprises” and/or “comprising,” when used in this specification, specify the presence of stated features, steps, elements, and/or components, but do not preclude the presence or addition of one or more other features, steps, elements, components, and/or groups thereof.
Furthermore, in accordance with the present invention there may be employed conventional molecular biology, microbiology, recombinant DNA and analytical techniques within the skill of the art. Such techniques are explained fully in the literature. See, e.g., Sambrook, Fritsch & Maniatis, Molecular Cloning: A Laboratory Manual, Second Edition (1989) Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. (herein “Sambrook et al., 1989”); DNA Cloning: A Practical Approach, Volumes 1 and 11 (D. N. Glover ed. 1985); Oligonucleotide Synthesis (M. J. Gait ed. 1984); Nucleic Acid Hybridization [B. D. Hames & S. J. Higgins eds. (1985)]; Transcription and Translation [B. D. Hames & S. J. Higgins, eds. (1984)]; Animal Cell Culture [R. 1. Freshney, ed. (1986)]; Immobilized Cells and Enzymes [IRL Press, (1986)]; B. Perbal, A Practical Guide to Molecular Cloning (1984); F. M. Ausubel et al. (eds.), Current Protocols in Molecular Biology, John Wiley & Sons, Inc. (1994); A Handbook of Bioanalysis and Drug Metabolism, G. Evans (2004).
An embodiment of the present invention is a method of identifying metabolic stability of a test agent due to semicarbazide-sensitive amine oxidase (SSAO) catalyzed metabolism, the method comprising: (a) culturing cells expressing SSAO; (b) adding a test agent to the cells; (c) incubating the test agent with the cells for a predetermined period of time; (d) measuring the amount of the test agent remaining in the presence of the cells comprising expressed SSAO at the predetermined period of time; and (e) comparing the amount of the test agent at the predetermined period of time to the amount of test agent in a control to determine a value wherein the value identifies the metabolic stability of the test agent in the presence of cells comprising expressed SSAO.
One skilled in the art will recognize that the method may be carried out using the cell lysate instead of the cells. Thus, an embodiment of the present invention is a method of identifying the metabolic stability of a test agent due to semicarbazide-sensitive amine oxidase (SSAO) catalyzed metabolism, the method comprising: (a) culturing cells expressing SSAO; (b) lysing the cells to form a cell lysate; (c) adding a test agent to the cell lysate; (d) incubating the test agent with the cell lysate for a predetermined period of time; (e) measuring the amount of the test agent remaining in the presence of the cell lysate comprising expressed SSAO at the predetermined period of time; and (f) comparing the amount of the test agent at the predetermined period of time to the amount of test agent in a control to determine a value wherein the value identifies the metabolic stability of the test agent in the presence of cell lysate comprising expressed SSAO. Another embodiment combines steps (b) and (c) into a single step.
A further embodiment of the present invention is a method of identifying the metabolic stability of a test agent due to SSAO catalyzed metabolism in a biological sample, the method comprising: (a) obtaining a biological sample comprising SSAO; (b) adding a test agent to the biological sample; (c) incubating the test agent with the biological sample for a predetermined period of time; (d) measuring the amount of the test agent at the predetermined period of time; and (e) comparing the amount of the test agent at the predetermined period of time to the amount of test agent in a control to determine a value wherein the value identifies the metabolic stability of the test agent in the presence of a biological sample comprising SSAO.
An embodiment of the present invention uses primary cell culture or cell lines that are commercially available. As a non-limiting example, cells that can be used are available from the American Tissue Culture Company. In one embodiment, CHO cells are used. Cells may be prokaryotic or eukaryotic. The scope of the invention is not limited by the type of cells used.
A biological sample may include, but is not limited to, tissue or fluids, sections of tissues such as biopsy and autopsy samples, and frozen sections taken for histologic purposes. Such samples include blood, sputum, tissue, cultured cells, (e.g., primary cultures, explants, and transformed cells), parts of or whole organs (e.g., liver, lung, ileum, artery, umbilical cord), stool, urine, etc. A biological sample can be obtained from an eukaryotic organism, including from mammals such as a primate, e.g., chimpanzee, macaque or human, cow, dog, cat, a rodent, e.g., guinea pig, rat, mouse, rabbit, or a bird, reptile, or fish. A non-limiting example of one embodiment of the instant invention is to investigate whether a particular test agent or compound has greater risk for metabolic liability or conversely is metabolically stable in one tissue compartment versus other tissue compartments, e.g., whether a compound has greater metabolic stability in liver compared to lung. Further, a biological sample can be processed to provide a suspension of its cellular components or used for primary culture of the cellular components.
An embodiment of the invention is to use a biological sample from a human or non-human subject to quantitate the metabolic stability of a test agent. A biological sample may be an organ sample derived from one or more organs of non-human animals or humans, a tissue sample derived from one or more tissues of non-human animals or humans, as well as cell samples, derived from one or more cells of non-human animals or humans or from cell cultures. For animal experimentation, biological samples may comprise target organ tissues obtained, for example, after necropsy or biopsy or may be body fluids, such as blood. For clinical use, samples may comprise body fluids, like blood, sera, plasma, urine, synovial fluid, spinal fluid, cerebrospinal fluid, semen or lymph, as well as body tissues obtained by biopsy. A reference or control is understood by one skilled in the art. A reference or control can include, but is not limited to, a biological sample from a non-diseased subject wherein the subject is a non-human animal or human. Further, a reference or control can be a biological sample from a non-treated subject. Alternatively, a reference or control can be from the same subject before, during and after treatment. A reference or control can be from the same subject but is a different cell, tissue or organ sample than the cell, tissue or organ source used to identify the metabolic stability of the test agent. A reference or control does not have to be a biological sample but can be a sample with a known amount of SSAO activity. A reference or control may be an agent that is not metabolized by SSAO or that is metabolized by SSAO with a known amount of SSAO liability.
The present invention provides methods for identifying the metabolic stability or metabolic liability of test agents. The term “test agent” as used herein describes any molecule, e.g. protein, non-protein organic compound or pharmaceutical, with the capability of being affected by or affecting the enzyme activity of SSAO. There are no particular restrictions as to the test agents that can be assayed. In an embodiment of the invention, a test agent is a compound. Examples of test agents include single agents or libraries of small, medium or high molecular weight chemical molecules. An agent can be in the form of a library of test agents, such as a combinatorial or randomized library that provides a sufficient range of diversity or conversely are limited to similar structures or features. Agents can be optionally linked to a fusion partner, e.g., targeting compounds, rescue compounds, dimerization compounds, stabilizing compounds, addressable compounds, and other functional moieties. Conventionally, new chemical entities with useful properties are generated by identifying a test agent (called a “lead compound” or a “lead”) with some desirable property or activity, e.g., inhibiting activity or modulating activity. The lead compound is then used as a scaffold to create variants of the lead compound, and further evaluate the property and activity of those variant compounds. One skilled in the art will appreciate the utility of using the instant invention to optimize compound selection by identifying metabolic stability and thus the metabolic liability of potential lead compounds and identifying or selecting those compounds with minimal liability to SSAO metabolism.
SSAO of the present invention is full-length SSAO or a fragment thereof that retains total or partial enzyme activity. Partial enzyme activity may be 30% of the total enzyme activity or greater, for example, 40% or 50%. A non-limiting example is an SSAO isolated from a species other than human. Non-limiting examples of other species include rodents such as rats, mice and guinea pigs or non-human primates such as monkeys or chimpanzees. A further non-limiting example is full-length human SSAO as disclosed in SEQ ID NO: 1 or fragments thereof having methyleneamine oxidase activity.
Metabolic stability or metabolic liability are terms of art understood by the skilled artisan. Metabolic stability refers to the susceptibility or extent to which a test agent or a drug molecule undergoes metabolism under a given condition. Thus, the higher the extent of metabolism, the lower the metabolic stability. Metabolic stability is one of several major determinants in defining the oral bioavailability and systemic clearance of a drug, compound or test agent. As a non-limiting illustration, after a drug is administered orally, it first encounters metabolic enzymes in the gastrointestinal lumen as well as in the intestinal epithelium. After it is absorbed into the bloodstream through the intestinal epithelium, it is delivered to the liver via the portal vein. A drug can be effectively cleared by intestinal or hepatic metabolism before it reaches systemic circulation, a process known as first pass metabolism. The stability or liability of a drug to metabolism within the liver as well as extra-hepatic tissues will ultimately determine the concentration of drug found in the systemic circulation and affect its half-life and residence time within the body. The type of biotransformations typically referred to as Phase I metabolism include oxidation, reduction, and hydrolysis which primarily serve to increase the hydrophilicity and enhance the excretion of a drug by unveiling or incorporating a polar functional group into the molecule (OH, SH, NH₂, or CO₂H). Phase 11 reactions or conjugation reactions further increase the polarity of a drug by modifying a functional group to form O- or N-glucuronides, sulfate esters, alpha-carboxyamides and glutathionyl adducts. An embodiment of the instant invention is the metabolic stability or metabolic liability of a drug, compound or test agent to metabolism by SSAO.
An embodiment of the invention selects the most relevant biological samples from human and other species to examine metabolic stability due to SSAO metabolism. For instance, liver-based metabolism is responsible for metabolic clearance of most drugs so concern in first pass metabolism may focus on hepatic and sometimes intestinal metabolism. The ubiquitous presence of SSAO in tissues and biological fluids and its particularly high activity in many tissues, such as lung and blood vessels, makes it imperative to use the appropriate biological samples in addition to or in place of liver to examine a test agent's metabolic stability in the presence of SSAO. In addition to intestinal and hepatic first-pass metabolism, the exposure of a test agent subject to SSAO may be limited by first pass metabolism at sites other than intestinal and hepatic tissues, such as portal veins, blood vessels, and lungs. A test agent may demonstrate different metabolic stability against different forms of SSAO. Different biological samples may contain different forms of SSAO. A non-limiting example is that a test agent may show relative metabolic stability against the soluble form of SSAO in human plasma but much higher metabolic instability against membrane-bound SSAO in tissues. Additionally, an animal species may show much higher or lower soluble SSAO activity in plasma than the level of soluble SSAO activity found in human, under comparable assay conditions.
An embodiment of the invention uses various chemical inhibitors to inhibit various forms of amine oxidase activities and attributes the observed metabolic instability as either SSAO catalyzed or monoamine oxidase (MAO)-A or MAO-B catalyzed metabolism. A non-limiting example is the addition of hydralazine as a non-discriminating amine oxidase inhibitor, clorgyline as a specific MAO-A inhibitor, pargyline as a mixed MAO-A and MAO-B inhibitor, semicarbazide and bromoethylamine as specific SSAO inhibitors.
Another non-limiting example of the invention is to determine the metabolic stability of a test agent in individuals treated with a drug or a combination of drugs to determine if there is a change in the metabolic stability of the test agent in such individuals compared to control subjects. One skilled in the art will appreciate the usefulness of obtaining biological samples from human or non-human subjects that suffer from one or more diseases or have been manipulated to induce one or more disease states, surgically or genetically altered or pretreated with a drug, compound or test agent. A non-limiting example includes using the invention to determine the metabolic stability of a test agent in organs that may be compromised by disease compared to non-diseased organs. As an additional non-limiting example, the metabolic stability of a compound can be assessed in lung tissue obtained from a human subject suffering from asthma and compared to the metabolic stability of the compound in healthy lung tissue from an age-matched or control subject. Another non-limiting example would be to study the metabolic stability of a compound in a biological sample such as in “young” liver compared to “old” or “aged” liver where “young”, “old” and “aged” are defined by the particular species under investigation.
An embodiment of the invention uses a homogeneous cell population or one biological sample. An alternative embodiment of the invention uses a heterogeneous cell population or a combination of more than one biological sample. The cells or biological sample can be of any type and in any proportion to complete the methods of the invention.
An embodiment of the invention uses a recombinant cell expressing SSAO. A recombinant expression vector of the invention comprises a nucleic acid molecule in a form suitable for expression of the nucleic acid in a host cell. Thus, a recombinant expression vector of the present invention can include one or more regulatory sequences, selected on the basis of the host cells to be used for expression, that is operably linked to the nucleic acid to be expressed. Within a recombinant expression vector, “operably linked” is intended to mean that the nucleotide sequence of interest is linked to the regulatory sequence(s) in a manner that allows for expression of the nucleotide sequence (e.g., in an in vitro transcription/translation system or in a host cell when the vector is introduced into the host cell). The term “regulatory sequence” is intended to include promoters, enhancers and other expression control elements (e.g., polyadenylation signals). Such regulatory sequences are described, for example, in Goeddel, Gene Expression Technology: Methods in Enzymology Vol. 185, Academic Press, San Diego, Calif. (1990). Regulatory sequences include those that direct constitutive expression of the nucleotide sequence in many types of host cells (e.g., tissue specific regulatory sequences). It will be appreciated by those skilled in the art that the design of the expression vector can depend on such factors as the choice of host cell to be transformed, the level of expression of protein desired, etc. The expression vectors of the invention can be introduced into host cells to produce proteins or peptides encoded by nucleic acids as described herein.
The term “overexpression” as used herein, refers to the expression of a polypeptide at a level that is greater than the normal level of expression of the polypeptide in a cell that normally expresses the polypeptide or in a cell that does not normally express the polypeptide. For example, expression of the polypeptide may by 10%, 20%, 30%, 40%, 50%, 60%, 70, 80%, 90%, 100%, or more as compared to expression of the polypeptide in a wild-type cell that normally expresses the polypeptide. Mutants, variants, or analogs of the polypeptide of interest may be overexpressed.
As used herein, the term “transient” expression refers to expression of exogenous nucleic acid molecule(s) which are separate from the chromosomes of the cell. Transient expression generally reaches its maximum 2-3 days after introduction of the exogenous nucleic acid and subsequently declines.
As used here, the term “stable” expression refers to expression of exogenous nucleic acid molecule(s) that have become an integrated part of the chromosome(s) of the cell. In general, vectors for stable expression of genes include one or more selection markers.
Cell culturing techniques for transformed, non-transformed, primary culture and biological samples are well known in the art. Biological samples or cultured cells can be stored until required for use. The media used for culturing can be specifically designed or purchased from commercial sources.
An embodiment of the invention involves lysing the cells. Cells can be lysed by the addition of a detergent containing lysis buffer. However, the invention is not limited to the use of detergent in the lysis buffer but may include any method that is appropriate for lysing cells. For example, cells may be lysed by exposure to hypertonic buffer, sonication or freeze/thaw. These and other methods of lysing cells are well known to those skilled in the art.
An embodiment of the invention uses a control. A control is a term of art well understood by skilled artisans. An appropriate control may be dependent on the assay parameters utilized or the experimental question under investigation. A control may be a particular set of assay conditions or the addition or elimination of a particular compound to the assay. Therefore, a non-limiting example of a control is a condition where a test agent is incubated in the absence of cells or cell lysates expressing SSAO. A control may be considered a positive control in that the assay conditions or control compound added brings about the anticipated response. For example, if the agent under investigation is expected to be metabolized, a positive control would be a compound that is metabolized by SSAO. Further, a positive control may be a compound that is metabolized by SSAO into known metabolic by-products. A non-limiting example of a positive control is the addition of benzylamine. A control may also be a negative control. A negative control may be a particular set of assay conditions or the addition or elimination of a particular compound to the assay that would not bring about the anticipated response. For example, if the agent under investigation is expected to be metabolized, then a negative control would be expected not to be metabolized. A non-limiting example of a negative control is the addition of benzyoic acid that does not have a methyleneamine group and is not metabolized by SSAO. A non-limiting example of a particular set of assay conditions as a negative control may be the addition of an inhibitor targeting SSAO enzyme activity, such as hydralazine, wherein the SSAO activity is inhibited. A control may be a “vehicle” control. For example, if the test agent is dissolved in DMSO then the vehicle control would be DMSO without test agent. A control may simply be the use of historical data.
An embodiment of the present invention is measuring the amount of the test agent incubated in the presence of SSAO at the predetermined period of time and comparing the amount of the test agent at the predetermined period of time to the amount of test agent in a control to determine the metabolic stability of the test agent in the presence of SSAO. It is readily apparent to one skilled in the art that metabolic stability of test agent can be measured by the disappearance of the test agent or alternatively by measuring the appearance of one or more metabolites of the test agent. A further embodiment of the present invention is to measure the appearance of one or more metabolites of the test agent in addition to or in place of measuring the amount of test agent.
The amount of test agent or the appearance of one or more metabolites of the test agent can be measured by any number of techniques available to one skilled in the art. Non-limiting examples include mass spectrometry, high-pressure liquid chromatography (HPLC), liquid chromatography/mass spectrometry, liquid chromatography/mass spectrometry/mass spectrometry and liquid chromatography/radiomatic detection. Further, the amount of test agent or the appearance of one or more metabolites of the test agent may be measured by the use of indicator molecules such as radioisotopes, fluorescent dyes or antibodies. The instant invention is not limited by the method of measuring the test agent or any one or more metabolites of the test agent.
The test agent may be labeled with a radioisotope, such as, but not limited to ³H or ¹⁴C. Thus, an embodiment of the invention is a method of identifying the metabolic stability of a radiolabeled test agent due to semicarbazide-sensitive amine oxidase (SSAO) catalyzed metabolism, the method comprising: (a) culturing cells expressing SSAO; (b) adding a radiolabeled test agent to the cells; (c) incubating the radiolabeled test agent with the cells for a predetermined period of time; and (d) measuring the amount of the radiolabeled test agent remaining in the presence of the cells comprising expressed SSAO at the predetermined period of time wherein the percentage of radiolabeled test agent that has not been metabolized identifies the metabolic stability of the radiolabeled test agent in the presence of cells comprising expressed SSAO. One skilled in the art will recognize the method may be carried out using cell lysates instead of the cells. Further, the instant invention is not limited by the use of radioisotopes but may use any means available in the art to label the test agent.
A further embodiment of the present invention is a method of identifying metabolic stability of a radiolabeled test agent due to SSAO catalyzed metabolism in a biological sample, the method comprising: (a) obtaining a biological sample comprising SSAO; (b) adding a radiolabeled test agent to the biological sample; (c) incubating the radiolabeled test agent with the biological sample for a predetermined period of time; and (d) measuring the amount of the radiolabeled test agent at the predetermined period of time wherein the percentage of radiolabeled test agent that has not been metabolized identifies the metabolic stability of the test agent in the presence of a biological sample comprising SSAO.
The skilled artisan can appreciate the usefulness of comparing the metabolic stability of a test agent in cells or cell lysates to the metabolic stability of the test agent in biological samples. Thus an embodiment of the present invention includes a method of determining the metabolic stability profile of a test agent, the method comprising (a) obtaining the value of metabolic stability of the test agent incubated in the presence of cells or cell lysate comprising expressed SSAO and (b) obtaining the value of metabolic stability of the test agent incubated in the presence of a biological sample comprising expressed SSAO wherein the value of metabolic stability of the test agent in the presence of the cells or cell lysate comprising expressed SSAO is compared to the value of metabolic stability of the test agent in the presence of the biological sample comprising SSAO providing the metabolic stability profile of the test agent.
Refinements such as using the present invention with high throughput screening (HTS) methods are well within the knowledge and capability of the skilled artisan and are considered embodiments of the invention. An embodiment of the invention is use in high throughput screening (HTS) methods. HTS is the automated, simultaneous testing of thousands of distinct chemical compounds in assays designed to model biological mechanisms or aspects of disease pathologies. More than one compound, e.g., a plurality of compounds, can be tested simultaneously. In one embodiment, the term HTS screening method refers to assays which test the metabolic stability of one compound in a plurality of biological samples or a plurality of compounds in one or more biological samples.
An embodiment of the present invention comprises an array of receptacles that can receive cells, cell lysates, bodily samples or other materials such as a methyleneamine or methyleneamine-like test agent under investigation. An array of receptacles can be any number of receptacles from at least one or more than one receptacle suitable for holding materials within the scope of the invention. Examples include but are not limited to flasks, culture dishes, slides, tubes such as 1.5 mL tubes, 12 well plates, 96 well plates, 384 well plates and miniaturized microtiter plates with perhaps 4000 receptacles (U.S. Patent Application 20050255580). The array of receptacles may be amendable to the addition of a protective covering thus preventing against entry of contaminants or evaporation of contents.
A further characteristic of the receptacles is that the receptacle may allow for analysis. Non-limiting examples include analysis by mass spectrometry or HPLC. However, there is not a limitation to receptacles that can be used within the scope of the present invention given that samples can be transferred to a suitable container for further analysis. A non-limiting example is to modify the method such that the method further comprises providing a second array of receptacles wherein one or more steps are performed in the second array of receptacles.
Liquid handling systems, analytical equipment such as fluorescence readers or scintillation counters and robotics for cell culture and sample manipulation are well known in the art. Mechanical systems such as robotic arms or “cherry-picking” devices are available to the skilled artisan. Commercial plate readers are available to analyze conventional 96-well or 384-well plates. Single sample, multiple sample or plate sample readers are available that analyze predetermined wells and generate raw data reports. The raw data can be transformed and presented in a variety of ways.
A further embodiment of the present invention is a kit comprising at least one element of an assay system to perform the methods disclosed herein and instructions for use. Thus, the components of the assay system may be provided separately or may be provided together in such a kit. Components of the assay system may be prepared and included in a kit according to methods that maximize the stability of the individual components. Such methods are familiar to those persons skilled in the art. For example, cells of the assay system may be provided as a suspension or the cells may be frozen or lyophilized. Additional components of the assay system may also be included such as buffers, containers for mixing the assay components such as microtiter plates or test tubes. The assay system can be provided in the form of a kit that includes instructions for performing the assay and instructions for data handling and interpretation.
The present invention is further described in the following examples, which do not limit the scope of the invention described in the claims. While the invention has been described and exemplified in sufficient detail for those skilled in this art to produce and use, various alternatives, modifications, and improvements should be apparent without departing from the spirit and scope of the invention. One skilled in the art readily appreciates that the present invention is well adapted to carry out the objective and obtain the ends and advantages mentioned, as well as those inherent therein. The examples that follow are descriptions of embodiments and are not intended as limitations on the scope of the invention. Modifications therein and other uses will occur to those skilled in the art. These modifications are encompassed within the spirit of the invention and are defined by the scope of the claims.
The present invention illustratively described herein may be practiced in the absence of any element or elements, limitation or limitations, which are not specifically disclosed herein. The terms and expressions which have been employed are used as terms of description and not of limitation, and there is no intention that in the use of such terms and expressions of excluding any equivalents of the features shown and described or portions thereof, but it is recognized that various modifications are possible within the scope of the invention claimed. Thus, it should be understood that although the present invention has been specifically disclosed by embodiments and optional features, modification and variation of the concepts herein disclosed may be made by those skilled in the art, and that such modifications and variations are considered to be within the scope of this invention as defined by the appended claims.

Example 1

A. Cloning and Expression of Human SSAO

1) In order to facilitate expression construct production, an initial pDONR221-full-length SSAO plasmid was generated as follows:
A first PCR was performed using gene-specific primers shown below. The forward primer has half of the att site (Invitrogen) and a Kozak sequence shown in bold. The reverse primer has the remaining half of the att site shown in bold. PCR was performed using human umbilical cord as the DNA template (prepared from RNA purchased from Biochain and Invitrogen's RT-PCR superscript 11 kit):

Initial Cloning Primers:

	Forward (SEQ ID NO: 3):
	5′-AAAAGCAGGCTTAGGAATGAACCAGAAGACAATCCTC-3′

	Reverse (SEQ ID NO: 4):
	5′-CAAGAAAGCTGGGTCCTAGTTGTGAGAGAAGCCCC-3′

A second PCR was then carried out using the universal primers shown below. The forward primer and the reverse primer included att site sequences (shown in bold) and vector sequences.

Universal Primer Sequences:

	Forward (SEQ ID NO: 5):
	5′-GGGGACAAGTTTGTACAAAAAAGCAGGCTTAGGA-3′

	Reverse (SEQ ID NO: 6):
	5′-GGGGACCACTTTGTACAAGAAAGCTGGGTC-3′

This second PCR product was cloned into pDONR221 using the Invitrogen BP reaction. Using this entry vector as template, six variations of human SSAO expression constructs were prepared; three forms (one full-length and two truncated) without tags and three with carboxyl-terminal 6×HIS tags to facilitate purification of the enzyme.
2) The full-length SSAO:
Sequences shown in bold on the forward primer and reverse primers indicate att site sequence.

Primer Sequences for Cloning Untagged, Full-length SSAO:

Forward (SEQ ID NO: 7):

5′-AAAAGCAGGCTTAGGAATGAACCAGAAGACAATCCTC-3′

Reverse (SEQ ID NO: 8):

5′-CAAGAAAGCTGGGTCCTAGTTGTGAGAGAAGCCCCCGTGG-3′

To add 3′ 6×HIS before the stop codon the following primers were used:
Sequences shown in bold on the forward primer and the reverse primer indicate att site sequence, underlined sequences on the reverse primer indicate the 6×HIS tag.
Primer Sequences for Cloning Full-length SSAO with C-terminal 6×HIS tag:
Forward (SEQ ID NO: 9):

5′-AAAAGCAGGCTTAGGAATGAACCAGAAGACAATCCTC-3′

Reverse (SEQ ID NO: 10):

5′-CAAGAAAGCTGGGTCCTAATGGTGATGGTGATGGTGGTTGTGAGAGA

AGCCCCCGTGG-3′

3) T₁(Gly27-Asn763) representing the enzyme lacking the membrane anchoring region:
Sequences shown in bold on the forward primer and the reverse primer indicate att site sequence, underlined sequences on the forward primer indicate additional N-terminal Met.

Primer Sequences for Cloning N-terminal Truncated, Untagged SSAO:

Forward (SEQ ID NO: 11):

5′-AAAAGCAGGCTTAGGA ATGGGCAGGGGTGGAGATGGGGGTG-3′

Reverse (SEQ ID NO: 12):

5′-CAAGAAAGCTGGGTCCTAGTTGTGAGAGAAGCCCC-3′

To add 3′ 6×HIS before the stop codon the following primers were used:
Sequences shown in bold on the forward primer and the reverse primer indicate att site sequence, underlined sequences on the forward primer indicate additional N-terminal Met, and underlined sequences on the reverse primer indicate the 6×HIS tag.

Primer Sequences for Cloning N-terminal Truncated, C-terminal 6×HIS tag SSAO:

Forward (SEQ ID NO: 13):

5′-AAAAGCAGGCTTAGGA ATGGGCAGGGGTGGAGATGGGGGTG-3′

Reverse (SEQ ID NO: 14):

5′-CAAGAAAGCTGGGTCCTAATGGTGATGGTGATGGTGGTTGTGAGAGA

AGCCCCCGTGG-3′

4) T₂(Met211-Asn763) representing the putative catalytic domain.
Sequences shown in bold on the forward primer and the reverse primer indicate att site sequence, and underlined sequences on the forward primer indicate additional N-terminal Met.
Primer Sequences for Cloning Catalytic domain of untagged SSAO:
Forward (SEQ ID NO: 15):

5′-AAAAGCAGGCTTAGGA ATGACCACGGCTCCCCGTGGTC-3′

Reverse (SEQ ID NO: 16):

5′-CAAGAAAGCTGGGTCCTAGTTGTGAGAGAAGCCCC-3′

To add 3′ 6×HIS before stop codon the following primers were used:
Sequences shown in bold on the forward primer and the reverse primer indicate att site sequence, underlined sequences on the forward primer indicate additional N-terminal Met, underlined sequences on the reverse primer indicate the 6×HIS tag.
Primer Sequences for Cloning Catalytic domain of SSAO with C-terminal 6×HIS tag:

Forward (SEQ ID NO: 17):

5′-AAAAGCAGGCTTAGGA ATGACCACGGCTCCCCGTGGTC-3′

Reverse (SEQ ID NO: 18):

5′-CAAGAAAGCTGGGTCCTAATGGTGATGGTGATGGTGGTTGTGAGAGA

AGCCCCCGTGG-3′

The expression constructs were prepared by cloning these PCR products into the pcDNA5-FRT-To-DEST vector (Invitrogen, Gateway System™). The forward and reverse DNA sequence of each construct was confirmed including expressed sequences and at least 100 base pairs either side of this. Stable cell lines for Flp-In CHO, Flp-In CHO T-Rex, and Flp-In HEK 293 (Invitrogen, Flp-In System™) were generated using these 6 constructs according to manufacturer's instructions. Cells were co-transfected with the regulatory vector, pOG44, and each of the pcDNA5-FRT-To-DEST constructs using Lipfectamine (Invitrogen) according to manufacturer's instructions. Thus, 18 cell lines were generated: CHO Flp-In full-length SSAO; CHO Flp-In full-length SSAO with C-terminal 6×HIS tag; CHO Flp-In T₁SSAO; CHO Flp-In T₁SSAO with C-terminal 6×HIS tag; CHO Flp-In T₂SSAO; CHO Flp-In T₂SSAO with C-terminal 6×HIS tag; CHO T-Rex Flp-In full-length SSAO; CHO T-Rex Flp-In full-length SSAO with C-terminal 6×HIS tag; CHO T-Rex Flp-In T₁SSAO; CHO T-Rex Flp-In T₁SSAO with C-terminal 6×HIS tag; CHO T-Rex Flp-In T₂SSAO; CHO Flp-In T₂SSAO with C-terminal 6×HIS tag; HEK 293 Flp-In full-length SSAO; HEK 293 Flp-In full-length SSAO with C-terminal 6×HIS tag; HEK 293 Flp-In T₁SSAO; HEK 293 Flp-In T₁SSAO with C-terminal 6×HIS tag; HEK 293 Flp-In T₂SSAO; HEK 293 Flp-In T₂SSAO with C-terminal 6×HIS tag.
Adherent CHO cells were cultured at 37° C., 5% CO₂in media containing Ham's F12, 10% fetal bovine serum, 2 mM L-glutamine, 1% Penicillin/Streptomycin, 300 μM hygromycin B. Adherent HEK 293 cells were cultured at 37° C., 5% CO₂in D-MEM (high glucose), 10% fetal bovine serum, 2 mM L-glutamine, and 200 μM hygromycin B. Stable transformants were identified by loss of zeocin resistance. Once the cells were 80% confluent, SSAO expression was induced by the addition of Tetracycline to 1 μg/mL. Following 18 hours, the cells were harvested using a trypsin treatment of 3 minutes, at room temperature. Cells were washed 3 times in phosphate buffered saline before flash freezing in liquid nitrogen.
For the preparation of cell lysate for activity testing, frozen cell pellets were resuspended in lysate buffer containing 10 mM Tris-HCl (pH 7.2), 150 mM NaCl, 1.5 mM MgCl₂, 1% v/v NP-40 and incubated for 15 minutes on ice. Lysate was cleared by centrifugation 800×g for 10 minutes, 4° C. and stored in aliquots at −80° C. until use. Proteins were determined using Pierce Coomassie Protein Reagent, according to manufacturer's instructions.

B. Testing the Recombinant Protein for Enzymatic Activity

(i). Sample Preparation.

For each assay run, 1 mL of cell lysate (1.5 mg/mL protein) was mixed with benzylamine to 2000 ng/mL final concentration. At each corresponding time point, 20 μL of the incubation mixture was transferred to a microcentrifuge tube (1.7 mL) and mixed with 50 μL of acetonitrile. The tubes were vortex mixed briefly to ensure complete mixing and then centrifuged at 10,000×g for 5 minutes. The supernatant was removed and 50 μL was transferred to an autosampler vial and mixed with 50 μL of water before LC/MS/MS analysis. Benzylamine remaining in the lysate was analyzed with LC/MS/MS method.

(ii). Analysis

LC/MS/MS analysis was performed with a PE Sciex API 3000 mass spectrometer under the following conditions listed below and in Tables 1 and 2:
Analytical column: Jupiter C-4, 5 μM, 50×2.1 mm
Column temperature: ambient
Flow rate: 0.2 mL/min
Injection volume: 15 μL
TABLE 1

Mobile Phase Gradient

Time (min) SolutionA (%) SolutionB (%)

0 40 60

0.1 95 5

2.9 95 5

3.0 40 60

6.0 40 60

SolutionA was 90% methanol in water, SolutionB was 10 mM ammonium acetate buffer, pH 7.0
Divert valve: 0-1.5 min to waste, 1.5-5 min to MS detector
TABLE 2

LC/MS/MS

Compound RT (min) Mass transition

Benzylamine 2.74 108.1 to 65.1 +Ve

(iii) Results of Cell Lysate LC/MS/MS Analysis are Shown in Table 3.

TABLE 3

SSAO Enzymatic Activity in Cell Lines Expressing Full-length
or Truncated SSAO

			Benzylamine
Source of Cell	SSAO		Remaining (%)

Lysate	Expressed	Tag	0 min	10 min	2 h

Control CHO	none	None	100	111	110
Control CHO Flp-In	none	None	100	104	99
CHO Flp-In	Full-	None	100	1	1
	length
CHO Flp-In	Full-	C-terminal	100	101	73
	length	6xHIS
CHO Flp-In	T1	None	100	109	103
CHO Flp-In	T1	C-terminal	100	101	98
		6xHIS
CHO Flp-In	T2	None	100	105	98
CHO Flp-In	T2	C-terminal	100	108	102
		6xHIS
CHO Flp-In T-Rex	None	None	100	104	99
CHO Flp-In T-Rex	Full-	None	100	6	0
	length
CHO Flp-In T-Rex	Full-	C-terminal	100	94	59
	length	6xHIS
CHO Flp-In T-Rex	T1	One	100	104	92
CHO Flp-In T-Rex	T1	C-terminal	100	95	93
		6xHIS
CHO Flp-In T-Rex	T2	None	100	97	83
CHO Flp-In T-Rex	T2	C-terminal	100	100	97
		6xHIS
HEK293 control	none	None	100	106	123
HEK293	Full-	None	100	58	2
	length
HEK293	Full-	C-terminal	100	105	98
	length	6xHIS
HEK293	T1	None	100	105	102
HEK293	T1	C-terminal	100	111	103
		6xHIS
HEK293	T2	None	100	113	101
HEK293	T2	C-terminal	100	100	117
		6xHIS

The active lysates from CHO Flp-In, CHO Flp-In T-Rex or HEK293 Flp-In expressing full-length SSAO (untagged) were subsequently tested and activity confirmed (Table 4). Since the most active SSAO cell lines was the CHO Flp-In expressing the full-length (untagged) SSAO, this preparation was used for subsequent activity testing.

TABLE 4

SSAO Enzymatic Activity in Cell Lines Expressing Full-length SSAO

Cell Type Expressing Full-

Benzylamine Remaining (%)

	length SSAO (untagged)	0 min	10 min	30 min

HEK293 Flp-In	100	50	9
CHO Flp-In	100	9	1
CHO Flp-In T-Rex	100	16	1

Example 2

Optimising LCMS/MS Assay Conditions

The Amplex Red assay (a commercially available assay), was used initially to measure the specific activity of the recombinant human SSAO. Amplex Red is a colorless and nonfluorescent derivative of dihydroresorufin. In the presence of amine oxidases and SSAO, the Amplex Red reacts with H₂O₂to produce the highly fluorescent product, resorufin. Resorufin has an excitation maximum at 563 nm and emission maximum at 587 nm and the assay can be quantified by reading the microtitre plate at 587 nm. The specific activity of recombinant SSAO was determined to be 280 pmol/min/mg protein and this was determined to be equivalent to the specific activity of SSAO found in human lung tissue. For subsequent assays to profile compounds in the LC/MS/MS assay, recombinant human SSAO (rhSSAO) was used at this defined specific activity.
The LC/MS/MS assay as described above was used to evaluate the susceptibility of compound A to metabolism by rhSSAO. The chemical structure of compound A is shown in FIG. 3 (U.S. Pat. No. 6,977,263 B2 generically encompasses molecules and methods of making the same). Compound A shown in Table 5 was incubated at 37° C. with rhSSAO (having a defined specific activity that is compatible with that found in human tissues as described above) for 4 hours initially or for 24 hours. At time zero and time 4 hours (or 24 hours), an aliquot of the sample was removed and quenched with acetonitrile. The samples were then analyzed by LC/MS/MS to measure the amount of parent compound remaining at 24 hours compared to that present at time zero.
The values shown in Table 5 are percent of parent compound remaining at the various times indicated following incubation with rhSSAO.

TABLE 5

Percent of Parent Compound Remaining
Following Incubation with rhSSAO
% Parent Compound Remaining

Compound	0 h (%)	4 h (%)	24 h (%)

A	100	25	3.2

Example 3

Testing of Metabolic Stability of Compound A in Supernatant Preparations of Human and Animal Tissue Homogenates

(i) Tissues used
The following tissues were used: lung, liver, and ileum from guinea pig, cynomolgus monkey, and human; artery from guinea pig and monkey; and umbilical cord from human.
(ii) Tissue preparation
Tissues were processed to obtain supernatants. Briefly, the excised tissues were rinsed immediately with copious amounts of physiological saline (prechilled to 4° C.) to remove blood. Pooled tissues were homogenized in chilled 0.01 M sodium phosphate buffer at pH 7.4 (10 mL per g tissue) with a Polytron. The homogenate was treated with Triton X-100 at an added concentration of ca. 1% under continuous gentle shaking for 2 hours at 4° C. and then centrifuged (4° C., 15 minutes, 3000×g). The supernatant was carefully separated and aliquoted into 2 mL portions and frozen at approximately −80° C. until use.
(iii) Optimization of Incubation Conditions with Test Compound
All incubations were conducted at 37° C. using a prewarmed water bath. ¹⁴C-radiolabeled test compound M.□were incubated at 1 or 10 Preliminary incubations were performed for each tissue/compound combination to select the appropriate incubation durations. Incubation durations of 1.5 to 6 hours were then used. Sufficient incubation volume was used to allow for at least five serial samples during the incubation duration. Individual aliquots (1 mL) taken from the incubation mixture were immediately quenched with two volumes of acetonitrile and the quenched mixtures were freeze-dried. The freeze-dried samples were either reconstituted immediately for sample analysis or stored at approximately −80° C. until analysis. Reconstitution was performed with a 500 L□ mixture (90% 20 mM ammonium acetate, pH 4.0 and 10% methanol (v/v)). L of the□After centrifugation, 100 reconstituted sample was injected for high performance liquid chromatographic (HPLC) separation followed by radiomatic detection.

(iv) Data Analysis and Calculations

Reconstituted samples from incubations were analyzed by HPLC followed by radiomatic detection. The identity of the test compound and respective benzylaldehyde and acid metabolites were verified by matching the retention times with the reference standards of the parent compound and their respective metabolites. The amount of the test compound remaining is calculated as the percent of the radioactivity of the parent peak in the total radioactivity of the radiochromatogram of a reconstituted sample. The percent of test compound remaining versus incubation time showed first-order kinetics when plotted on a log-linear scale. The first-order rate constant was calculated for individual incubations as the slope between the logarithm of the test compound remaining versus time based on least square linear regression analysis.

(v) Results of Test Compound Metabolic Stability in Tissue Preparations

The first-order rate constant (1/h) for the metabolic degradation of the test compound is listed in Table 6. Assuming that the metabolism followed Michaelis-Menten kinetics, the approximation to first-order kinetics M implied that K□for up to 10_m>>M for the enzymatic reaction.□10

TABLE 6

Metabolic Stability of Compound A in Tissue Preparations

Compound A

	Species	Tissue	M□1	M□10

Human	Liver	0.418	0.365
	Ileum	0.352	0.353
	Lung	0.675	0.706
	Umbilical cord	0.688	0.697
Guinea pig	Liver	0.318	0.305
	Ileum	0.0775	0.0782
	Lung	0.747	0.709
	Artery	0.127	0.111
Monkey	Liver	2.05	2.64
	Ileum	0.328	0.277
	Lung	0.177	0.208
	Artery	0.835	0.673

As shown Table 6, the present invention demonstrates a good correlation between the tissue data and the observed clinical metabolic profile of compound A. Compared to using only human plasma stability measurements, the present invention can better reflect human SSAO stability of a pharmaceutical agent under physiological conditions and is a more relevant predictive tool for guiding the selection of and the pharmaceutical development of clinical candidates.

Claims

1. A method of identifying metabolic stability of a test agent due to semicarbazide-sensitive amine oxidase (SSAO) catalyzed metabolism, the method comprising:

a) culturing cells expressing SSAO;

b) adding a test agent to the cells;

c) incubating the test agent with the cells for a predetermined period of time;

d) measuring the amount of the test agent remaining in the presence of the cells comprising expressed SSAO at the predetermined period of time; and

e) comparing the amount of the test agent at the predetermined period of time to the amount of test agent in a control to determine a value

wherein the value identifies the metabolic stability of the test agent in the presence of cells comprising expressed SSAO.

2. A method of identifying metabolic stability of a radiolabeled test agent due to semicarbazide-sensitive amine oxidase (SSAO) catalyzed metabolism, the method comprising:

a) culturing cells expressing SSAO;

b) adding a radiolabeled test agent to the cells;

c) incubating the radiolabeled test agent with the cells for a predetermined period of time; and

d) measuring the amount of the radiolabeled test agent remaining in the presence of the cells comprising expressed SSAO at the predetermined period of time;

wherein the percentage of radiolabeled test agent that has not been metabolized identifies the metabolic stability of the radiolabeled test agent in the presence of the cells comprising expressed SSAO.

3. The method of claim 1 or claim 2 wherein the cells expressing SSAO are produced by transient or stable transfection of the cells with DNA encoding SSAO.

4. The method of claim 1 or claim 2 wherein the cells expressing SSAO are prokaryotic.

5. The method of claim 1 or claim 2 wherein the cells expressing SSAO are eukaryotic.

6. A method of identifying metabolic stability of a test agent due to SSAO catalyzed metabolism in a biological sample, the method comprising:

a) obtaining a biological sample comprising SSAO;

b) adding a test agent to the biological sample;

c) incubating the test agent with the biological sample for a predetermined period of time;

d) measuring the amount of the test agent at the predetermined period of time; and

wherein the value identifies the metabolic stability of the test agent in the presence of a biological sample comprising SSAO.

7. A method of identifying metabolic stability of a radiolabeled test agent due to SSAO catalyzed metabolism in a biological sample, the method comprising:

a) obtaining a biological sample comprising SSAO;

b) adding a radiolabeled test agent to the biological sample;

c) incubating the radiolabeld test agent with the biological sample for a predetermined period of time; and

d) measuring the amount of the radiolabeled test agent at the predetermined period of time

wherein the percentage of radiolabeled test agent that has not been metabolized identifies the metabolic stability of the test agent in the presence of a biological sample comprising SSAO.

8. The method of claim 6 or claim 7 wherein the biological sample is selected from the group consisting of blood, plasma, serum, artery, umbilical cord, liver, ileum, and lung.

9. The method of claim 8 wherein the biological sample is from a human subject.

10. The method of claim 8 wherein the biological sample is from a non-human subject.

11. The method of claim 9 or claim 10 wherein the human or non-human subject is manipulated prior to obtaining the biological sample.

12. The method of claim 11 wherein the manipulation of the human or non-human subject is selected from the group consisting of treatment with one or more drugs, induction of one or more aspects of a disease state, surgical manipulation and genetic alteration.

13. The method of claim 1 or claim 6 wherein the amount of test agent is determined by a technique selected from the group consisting of mass spectrometry, high-pressure liquid chromatography, liquid chromatography/mass spectrometry, liquid chromatography/mass spectrometry/mass spectrometry and liquid chromatography/radiomatic detection.

14. The method of claim 1 or claim 6 wherein one or more steps are performed by a robotic device.

15. The method of claim 1 or claim 6 wherein the metabolic stability of the test agent is determined by measuring one or more metabolites of the test agent in addition to or in place of measuring the test agent.

16. A method of determining the metabolic stability profile of a test agent, the method comprising:

a) obtaining the value of metabolic stability of the test agent incubated in the presence of the cell comprising expressed SSAO using the method of claim 1;

b) obtaining a biological sample comprising SSAO;

c) adding a test agent to the biological sample;

d) incubating the test agent with the biological sample for a predetermined period of time;

e) measuring the amount of the test agent at the predetermined period of time; and

f) comparing the amount of the test agent at the predetermined period of time to the amount of test agent in a control to determine a value that identifies the metabolic stability of the test agent in the presence of a biological sample comprising SSAO

wherein the value of metabolic stability of the test agent in the presence of the cell comprising expressed SSAO is compared to the value of metabolic stability of the test agent in the presence of a biological sample comprising SSAO providing the metabolic stability profile of the test agent.

17. A method of determining the metabolic stability profile of a radiolabeled test agent, the method comprising:

a) obtaining the value of metabolic stability of the radiolabeled test agent incubated in the presence of the cell lysate comprising expressed SSAO using the method of claim 2;

b) obtaining a biological sample comprising SSAO;

c) adding a radiolabeled test agent to the biological sample;

d) incubating the radiolabeled test agent with the biological sample for a predetermined period of time;

e) measuring the amount of the radiolabeled test agent at the predetermined period of time; and

f) identifying the metabolic stability of the radiolabeled test agent by the percentage of radiolabeled test agent that has not been metabolized at the predetermined period of time

wherein the value of metabolic stability of the radiolabeled test agent in the presence of cell lysate comprising expressed SSAO is compared to the value of metabolic stability of the radiolabeled test agent in the presence of a biological sample comprising SSAO providing the metabolic stability profile of the test agent.