# US 11,442,064 B2 · Mass spectrometric methods and kits to identify a microorganism > Agents: this data is available as JSON from the patentgrep API and MCP server — see https://patentgrep.com/llms.txt - Number: US 11,442,064 B2 - Document ID: US11442064B2 - Status: Granted - Kind: B2 - Application number: 16/328,233 - Filed: 2017-08-24 - Published: 2019-07-11 - Granted: 2022-09-13 - Earliest claimed: 2016-08-25 - Assignees: Thermo Fisher Scientific Inc. - Applicants: Thermo Fisher Scientific Oy - Inventors: Mikko Koskinen; Leena Valmu; Joni Rannisto; Kelly Flook; Roger Grist; Anssi Rantakari - Web page: https://patentgrep.com/patent/US11442064B2 ## CPC - G01N 33/56944: {Streptococcus} - G01N 33/569: for microorganisms, e.g. protozoa, bacteria, viruses - G01N 33/56911: {Bacteria} - G01N 33/56916: {Enterobacteria, e.g. shigella, salmonella, klebsiella, serratia} - G01N 33/56938: {Staphylococcus} - G01N 33/56961: {Plant cells or fungi} - G01N 33/6848: {Methods of protein analysis involving mass spectrometry} - 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) ## Abstract The present invention includes a novel method and system for identification of microorganisms in samples that proteins and other biological material from non-microorganism sources (e.g., proteins of mammalian origin) that can interfere with identification of the microorganisms. The methods and systems described herein include use of a single-use chromatography medium to purify intact proteins prior to mass spectrometry analysis. The chromatography medium and the methods described herein can rapidly and efficiently remove of a substantial portion of interfering biological material (e.g., mammalian proteins) from a crude cell lysate while preserving high signal strength and removing enough of the interfering protein(s) to allow for identification of the microorganism(s) by mass spectrometry analysis. ## Claims ### Claim 1 A method for identifying a microorganism in a fluid comprising one or more interfering mammalian proteins, the method comprising: preparing a lysate from the fluid, the lysate comprising a microorganism protein and an interfering mammalian protein from the group consisting of defensins and proteolysis products thereof; contacting the lysate with a chromatography medium, wherein hemoglobin, defensins or proteolysis products thereof and the microorganism protein bind to the chromatography medium; selectively eluting proteins bound to the chromatography medium to produce at least one eluted fraction, wherein the at least one eluted fraction is enriched in the microorganism protein and depleted in defensins or proteolysis products thereof; and subjecting the at least one eluted fraction to protein mass spectrometry analysis and thereby identifying the microorganism in the fluid. ### Claim 2 (depends on 1) The method of claim 1, wherein the fluid is urine or cerebrospinal fluid. ### Claim 3 (depends on 1) The method of claim 1, further comprising separating cell fragments and unlysed microorganism cells from the lysate. ### Claim 4 (depends on 3) The method of claim 3, further comprising: contacting the fluid with a lysing agent selected to lyse mammalian cells in the fluid but not a microorganism cell; separating the microorganism cell from the lysed mammalian cells; and washing the microorganism cell. ### Claim 5 (depends on 1) The method of claim 1, wherein contacting the lysate with the chromatography medium includes: providing an extraction cartridge that contains a bed of the chromatography medium; adding the lysate to the extraction cartridge and allowing the lysate to flow through the bed of chromatography media; and adding a wash buffer to the extraction cartridge and allowing the wash buffer to flow through the bed of chromatography media; and selectively eluting proteins bound to the chromatography medium with an elution buffer. ### Claim 6 (depends on 4) The method of claim 4, wherein the extraction cartridge is inline in a liquid chromatography system and the lysate is added to the extraction cartridge by a pump. ### Claim 7 (depends on 5) The method of claim 5, wherein the elution buffer comprises water and acetonitrile in a range of 10 vol % acetonitrile to 60 vol % acetonitrile. ### Claim 8 (depends on 1) The method claim 1, wherein the protein mass spectrometry analysis is one of MALDI or ESI-MS. ### Claim 9 (depends on 1) The method claim 1, wherein the chromatography medium is selected from the group consisting of reversed-phase media, normal phase media, ion exchange media, affinity chromatography media, size exclusion media, hydrophobic interaction media, and combinations thereof. ### Claim 10 (depends on 1) The method of claim 1, wherein the chromatography medium is prepared from monomers selected from the group consisting of substituted or unsubstituted vinyl containing monomers, substituted or unsubstituted acrylate containing monomers, substituted or unsubstituted methacrylate containing monomers, acrylamide, fluoro-substituted ethylene, polymers selected from the group consisting of polyolefin, polyester, polyurethane, polyamide, and combinations thereof. ### Claim 11 (depends on 10) The method of claim 10, wherein the monomers include a mixture of at least two monomers present in an amount of from 10 vol. % to 70 vol. %. ### Claim 12 (depends on 1) The method of claim 1, wherein the chromatography medium is prepared from a mixture of any two or more of: divinyl benzene, styrene, and ethylvinylbenzene. ### Claim 13 A method for identifying a microorganism in a fluid comprising one or more interfering mammalian proteins, the method comprising: preparing a lysate from the fluid, the lysate comprising a microorganism protein and an interfering mammalian protein from the group consisting of hemoglobin, defensins and proteolysis products thereof; passing the lysate through an extraction cartridge, the extraction cartridge comprising: a column body having a reservoir portion, an extraction media portion, and a collar portion; wherein the reservoir portion includes an inlet and a reservoir; wherein the extraction media portion includes an elongated sleeve having an inner surface defining a cavity having a chromatography medium therein, said elongated sleeve further having an inlet end in fluid communication with the reservoir and an outlet end disposed remote from the inlet end, the chromatography medium extending substantially to the outlet end of the elongated sleeve; wherein the collar portion extends axially in a common direction with the elongated sleeve and has a terminal end which is spaced apart from the outlet end of the elongated sleeve and which extends axially at least to a plane defined by the outlet end of the elongated sleeve; and wherein the interfering mammalian protein and the microorganism protein bind to the chromatography medium; selectively eluting proteins bound to the chromatography medium to produce at least one eluted fraction, wherein the at least one eluted fraction is enriched in the microorganism protein and depleted in hemoglobin, defensins or proteolysis products thereof; and subjecting the at least one eluted fraction to protein mass spectrometry analysis and thereby identifying the microorganism in the fluid. ### Claim 14 (depends on 13) The method of claim 13, wherein the fluid is blood, a blood culture, urine or cerebrospinal fluid. ### Claim 15 (depends on 13) The method of claim 13, further comprising separating cell fragments and unlysed microorganism cells from the lysate. ### Claim 16 (depends on 15) The method of claim 15, further comprising: contacting the fluid with a lysing agent selected to lyse mammalian cells in the fluid but not a microorganism cell; separating the microorganism cell from the lysed mammalian cells; and washing the microorganism cell. ### Claim 17 (depends on 13) The method of claim 13, further comprising, after passing the lysate through the extraction cartridge and prior to selectively eluting proteins bound to the chromatography medium, adding a wash buffer to the extraction cartridge and allowing the wash buffer to flow through the chromatography medium. ### Claim 18 (depends on 13) The method of claim 13, wherein the extraction cartridge is inline in a liquid chromatography system and the lysate is added to the extraction cartridge by a pump. ### Claim 19 (depends on 13) The method of claim 13, wherein the step of selectively eluting proteins bound to the chromatography medium comprises selectively eluting the proteins using an elution buffer that comprises water and acetonitrile in a range of 10 vol % acetonitrile to 60 vol % acetonitrile. ### Claim 20 (depends on 13) The method of claim 13, wherein the protein mass spectrometry analysis is one of MALDI or ESI-MS. ### Claim 21 (depends on 13) The method claim 13, wherein the chromatography medium is selected from the group consisting of reversed-phase media, normal phase media, ion exchange media, affinity chromatography media, size exclusion media, hydrophobic interaction media, and combinations thereof. ### Claim 22 (depends on 13) The method of claim 13, wherein the chromatography medium is prepared from monomers selected from the group consisting of substituted or unsubstituted vinyl containing monomers, substituted or unsubstituted acrylate containing monomers, substituted or unsubstituted methacrylate containing monomers, acrylamide, fluoro-substituted ethylene, polymers selected from the group consisting of polyolefin, polyester, polyurethane, polyamide, and combinations thereof. ### Claim 23 (depends on 22) The method of claim 22, wherein the monomers include a mixture of at least two monomers present in an amount of from 10 vol. % to 70 vol. %. ### Claim 24 (depends on 13) The method of claim 13, wherein the chromatography medium is prepared from a mixture of any two or more of: divinyl benzene, styrene, and ethylvinylbenzene.