# US 8,592,167 B2 · Enzyme detection device > Agents: this data is available as JSON from the patentgrep API and MCP server — see https://patentgrep.com/llms.txt - Number: US 8,592,167 B2 - Document ID: US8592167B2 - Status: Granted - Kind: B2 - Application number: 12/674,603 - Filed: 2008-08-26 - Published: 2012-06-14 - Granted: 2013-11-26 - Earliest claimed: 2007-08-23 - Assignees: Mologic Limited - Applicants: Paul James Davis - Inventors: Paul James Davis - Web page: https://patentgrep.com/patent/US8592167B2 ## CPC - G01N 33/573: for enzymes or isoenzymes - C12Q 1/37: involving peptidase or proteinase - G01N: INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES (measuring or testing apparatus or processes other than immunoassay, involving enzymes or microorganisms C12M, C12Q) - C12Q: MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS (immunoassay G01N33/53); COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES ## Abstract An enzyme detection device (1) for detecting the presence, in a sample, of an enzyme capable of modifying a provided substrate (10). The device (1) comprises a substrate which has a modification region (14) that is sensitive to modification by the enzyme from an unmodified state to a modified state. The device (1) further comprises a substrate recognition molecule (16) which binds the modification region (14) in either the modified or the unmodified state. The modification region 14 of the substrate is preferentially bound by the substrate recognition molecule (16) as compared with the enzyme when mixed. The device further comprises a detectable label (18) coupled to the substrate recognition molecule (17). ## Claims ### Claim 1 A method of detecting an enzyme capable of modifying a substrate comprising the steps of: (i) providing a substrate comprising an attachment region and a modification region sensitive to modification by the enzyme from an unmodified state to a modified state, providing a solid support and attaching the attachment region of the substrate to the solid support by providing a first capture recognition molecule, capable of binding the attachment region, on the solid support; (ii) providing a sample suspected of containing the enzyme; (iii) providing a substrate recognition molecule to which is coupled a detectable label, wherein the substrate recognition molecule specifically binds the modification region in the unmodified state, the binding site of the substrate recognition molecule being such that the modification region of the substrate is preferentially bound by said substrate recognition molecule as compared with the enzyme when the substrate, substrate recognition molecule and enzyme are mixed, and wherein the substrate recognition molecule sequesters the modifiable region of the substrate, and in doing so it prevents the enzyme from modifying the substrate further; (iv) mixing the sample and substrate such that at least some of the enzyme in the sample modifies the substrate; and (v) bringing the substrate and the substrate recognition molecule into contact and detecting the presence of the label wherein detection of the label indicates the absence of the enzyme. ### Claim 2 A method of delecting an enzyme capable of modifying a substrate comprising the steps of: (i) providing a substrate comprising an attachment region and a modification region sensitive to modification by the enzyme from an unmodified state to a modified stale; (ii) providing a sample suspected of containing the enzyme; (iii) providing a substrate recognition molecule to which is coupled a detectable label, wherein the substrate recognition molecule specifically binds the modification region in the unmodified state, the binding site of the substrate recognition molecule being such that the modification region of the substrate is preferentially bound by said substrate recognition molecule as compared with the enzyme when the substrate, substrate recognition molecule and enzyme are mixed, and wherein the substrate recognition molecule sequesters the modifiable region of the substrate, and in doing so it prevents the enzyme from modifying the substrate further; (iv) mixing the sample and substrate such that at least some of the enzyme in the sample modifies the substrate; (v) depositing the substrate and the substrate recognition molecule on or in a chromatographic medium, wherein the chromatographic medium comprises a first capture recognition molecule immobilised on or in the chromatographic medium, the first capture recognition molecule being capable of binding the attachment region, bringing the substrate and the substrate recognition molecule into contact and detecting the presence of the label wherein detection of the label indicates the absence of the enzyme. ### Claim 3 (depends on 1, 2) The method according to claims 1 or 2 wherein the attachment region is an unmodifiable ligand. ### Claim 4 (depends on 2) The method according to claim 2 further comprising a second capture recognition molecule immobilised on or in the chromatographic medium, the second capture recognition molecule being capable of binding the substrate recognition molecule, optionally in combination with a fragment of the substrate, wherein the method further comprises the step of detecting the presence of the substrate recognition molecule at the second capture recognition molecule. ### Claim 5 (depends on 1, 2) The method according to claims 1 or 2 wherein the enzyme is a hydrolase, preferably a peptidase, lipase, nuclease, homo- or hetero-oligosaccharidedase, homo or hetero-polysaccharidase, carbohydrase, phosphatase, sulphatase, neuraminidase, esterase, DNAase, RNAase, a kinase, a glycosyl transferase, an oxidase, a reductase or a transaminase. ### Claim 6 (depends on 1, 2) The method according to claims 1 or 2 wherein the label is covalently bound to the substrate recognition molecule; and/or wherein the label is a fluorophore, a gold particle, a chromogen, a luminescent compound, a radioactive compound, a visible compound, a liposome or other vesicle containing signal producing substances, an electroactive species, or a combination of an enzyme and its substrate. ### Claim 7 (depends on 1, 2) The method according to claims 1 or 2 wherein step (i) further comprises providing an additional substrate, the additional substrate also comprising a modification region, the modification region of the substrate being sensitive to modification by a first enzyme, the modification region of the additional substrate being sensitive to modification by a second enzyme and wherein step (iii) further comprises providing an additional substrate recognition molecule, the additional substrate recognition molecule specifically binding the modification region of the additional substrate, in the unmodified state, the modification region of the additional substrate being preferentially bound by said additional substrate recognition molecule as compared with the second enzyme and wherein step (v) comprises detecting the interaction between the substrate and additional substrate and the substrate recognition molecule and additional substrate recognition molecule respectively. ### Claim 8 (depends on 1, 2) An enzyme detection device for carrying out the method according to claim 1 or claim 2. ### Claim 9 (depends on 1) The method according to claim 1 further comprising a second capture recognition molecule immobilised on or in the solid support, the second capture recognition molecule being capable of binding the substrate recognition molecule, optionally in combination with a fragment of the substrate, wherein the method further comprises the step of detecting the presence of the substrate recognition molecule at the second capture recognition molecule.