US20050170426A1 - Device for binding molecules, molecular groups, molecular parts and/or cells - Google Patents

Device for binding molecules, molecular groups, molecular parts and/or cells Download PDF

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Publication number
US20050170426A1
US20050170426A1 US11/089,304 US8930405A US2005170426A1 US 20050170426 A1 US20050170426 A1 US 20050170426A1 US 8930405 A US8930405 A US 8930405A US 2005170426 A1 US2005170426 A1 US 2005170426A1
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US
United States
Prior art keywords
molecular
object holder
liquid
duct
cells
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US11/089,304
Inventor
Walter Schubert
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
MPB Meltec Patent und Beteiligungs GmbH
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MPB Meltec Patent und Beteiligungs GmbH
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Priority to US11/089,304 priority Critical patent/US20050170426A1/en
Assigned to MPB MELTEC PATENT - UND BETEILIGUNGSGESELLSCHAFT MBH reassignment MPB MELTEC PATENT - UND BETEILIGUNGSGESELLSCHAFT MBH ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: SCHUBERT, WALTER
Publication of US20050170426A1 publication Critical patent/US20050170426A1/en
Abandoned legal-status Critical Current

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    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N1/00Sampling; Preparing specimens for investigation
    • G01N1/28Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
    • G01N1/30Staining; Impregnating ; Fixation; Dehydration; Multistep processes for preparing samples of tissue, cell or nucleic acid material and the like for analysis
    • G01N1/31Apparatus therefor
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S436/00Chemistry: analytical and immunological testing
    • Y10S436/807Apparatus included in process claim, e.g. physical support structures
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T436/00Chemistry: analytical and immunological testing
    • Y10T436/25Chemistry: analytical and immunological testing including sample preparation
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T436/00Chemistry: analytical and immunological testing
    • Y10T436/25Chemistry: analytical and immunological testing including sample preparation
    • Y10T436/2575Volumetric liquid transfer

Definitions

  • the present invention relates to a device for binding molecules, molecular groups, molecular parts and/or cells contained in a liquid to target structures, as well as to a method for binding molecules, molecular groups, molecular parts and/or cells contained in a liquid to target structures.
  • a device of the invention for binding molecules, molecular groups, molecular parts and/or cells contained in a liquid to target structures comprises at least one object holder with at least one target structure firmly held therein which is in contact with at least one duct made of at least one material, said duct including, at its one aperture, a liquid inlet and, at its other aperture, a liquid outlet, as well as at least one object holder thermostat used for cooling the respective object holder.
  • the duct is formed by the object holder and paraffin-like sheet material. This allows the duct to widen, if necessary, preventing excessive pressure build-up within said duct.
  • the discharged liquid will be collected in a vessel, thus preventing a loss of liquid which has already passed the duct, which liquid may be difficult and/or expensive to prepare.
  • the temperature of the vessel will be cooled by a vessel thermostat, thus preventing any metabolic processes from occurring within said vessel and allowing the liquid or its ingredients to be used again.
  • a method of the invention for binding molecules, molecular groups, molecular parts and/or cells contained in a liquid to target structures comprises the following steps: (a) passing liquid through a duct and over an object holder carrying a target structure firmly held therein, (b) removing any non-binding matter via a second duct aperture and collecting such matter in a vessel, (c) cooling said object holder by means of an object holder thermostat, and (d) fixing the molecules, molecular groups, molecular parts and/or cells adhering to the object holder.
  • the device is used in an automated method for determining molecular classes, molecular groups, molecular parts in a solid or liquid object according to U.S. patent application Ser. No. 09/353,942, the entire specification of which is incorporated herein by this reference.
  • This will allow identification and characterization of the binding partners. It will be possible at the same time to identify and characterize the molecular classes, molecular groups and/or molecular parts required for the binding process.
  • Such application will be advantageous in numerous areas of chemistry, biology, biochemistry and especially medicine. This will not only open up new possible ways of diagnosing, but will also provide a new test system for therapeutic approaches on a molecular level.
  • FIG. 1 a is a top view of an object holder of the device of the invention
  • FIG. 1 b is a cross-sectional view of the object holder of FIG. 1 a;
  • FIG. 2 a is a schematic lateral view of the device of the invention.
  • FIG. 2 b is a detailed view of an element of the device of the invention.
  • FIG. 1 a is a top view of an object holder 10 of the device for binding molecules, molecular groups, molecular parts and/or cells
  • FIG. 1 b is a cross-sectional view of the object holder 10 .
  • a target structure 12 has been detachably mounted on said object holder 10 and contacts a duct 14 defined by said object holder 10 , two paraffin-sheet strips 20 and a continuous paraffin-sheet layer 22 .
  • Two aluminum rails 24 are mounted on said paraffin-sheet layer 22 whose surface areas are similar to that of said paraffin-sheet strips 20 underneath them.
  • duct 14 has first and second duct apertures 16 , 18 for inlet and outlet, resp., of liquid 62 .
  • Liquid 62 may be discharged by means of a plunger mechanism 58 , a pump (not shown), or under the influence of gravity and by means of a pump (not shown), or under the influence of gravity alone.
  • FIG. 2 a is a schematic lateral view of the device for binding molecules, molecular groups, molecular parts and/or cells, with said object holder 10 , including paraffin-sheet strips 20 , paraffin-sheet layer 22 , aluminum rails 24 , a hollow needle 60 and said liquid 62 , being additionally shown in detail in FIG. 2 b.
  • the device includes an object holder thermostat 26 comprising a cooling plate 28 , made of aluminum, a first Peltier element 30 , a first cooling element 32 and a first fan 34 .
  • Said device is mounted on a post 52 with clamping joint 54 in such a way that the angle between the mounted object holder 10 and a basic plate 64 is approx. 20-70°.
  • Object holder 10 is firmly pressed onto object holder thermostat 26 by a pressure plate with a central aperture 36 which rests on aluminum rails 24 . Sufficient pressure is ensured by way of springs 38 .
  • Liquid 62 is introduced into the first duct aperture 16 by means of a suture 58 detachably mounted by means of a suture support 56 , and a hollow needle. Under the influence of gravity, liquid 62 will thus flow through duct 14 and contact target structure 12 , allowing the desired and predetermined ingredients of liquid 62 to bind to target structure 12 . Finally, liquid 62 will reach the second duct aperture 18 , exit duct 14 and drip into a vessel 40 surrounded by a vessel thermostat 42 .
  • Said vessel thermostat 42 comprises a vessel support 44 , made of copper, a second Peltier element 46 , a second cooling element 48 and a second fan 50 .
  • object holder thermostat 26 and vessel thermostat 42 will cool said vessel 40 and said object holder 10 down to 4° C. so as to stop any metabolic activity.
  • Liquid 62 may contain lymphocytes.
  • Target structure 12 is a tissue section or a membrane coated with molecules or molecular combinations.

Abstract

The present invention relates to a device for binding molecules, molecular groups, molecular parts and/or cells contained in a liquid to target structures, the device having at least one object holder with at least one target structure firmly held therein and which contacts at least one duct made of at least one material. One aperture of the duct is a liquid inlet aperture, and a second aperture is a liquid outlet aperture. At least one object holder thermostat is used for cooling the object holder.

Description

  • The present invention relates to a device for binding molecules, molecular groups, molecular parts and/or cells contained in a liquid to target structures, as well as to a method for binding molecules, molecular groups, molecular parts and/or cells contained in a liquid to target structures.
  • The only method known so far for binding molecules, molecular groups, molecular parts and/or cells contained in a liquid to target structures is the one according to “Stamper and Woodruff (1976) J. Exp. Med. 144, 828-833”. This method comprises the fixing of target structures to a surface and subsequently rehydrating them. Then, the target structures are coated with 100 to 200 μl of the liquid containing the molecules, groups of molecules, parts of molecules and/or cells. Incubation (e.g.: 30 min, 7° C.) thereof on a shaker or rotating table is followed by a rinsing step which will remove any non-binding matter.
  • One major disadvantage of this method is the fact that it is performed manually. Moreover, motion devices are used for obtaining the binding equilibrium which only poorly simulate the conditions prevailing in certain natural systems. Another shortcoming is that the rinsing step may destroy the often weak adherence of ingredients of the liquid to the target structures. Yet another disadvantage of this method is that it is not capable of stopping metabolic processes.
  • It is therefore the object of the present invention to provide a device and a method for simulating the short-term interactions occurring between molecules, molecular groups, molecular parts and/or cells in a liquid, on the one hand, and the target structures, on the other, at the same time allowing most of the metabolic processes to be stopped at any time.
  • This object is accomplished by a device and a method having the features of the independent claims.
  • Advantageous embodiments are described in the subclaims.
  • A device of the invention for binding molecules, molecular groups, molecular parts and/or cells contained in a liquid to target structures comprises at least one object holder with at least one target structure firmly held therein which is in contact with at least one duct made of at least one material, said duct including, at its one aperture, a liquid inlet and, at its other aperture, a liquid outlet, as well as at least one object holder thermostat used for cooling the respective object holder.
  • This is based on the inventive idea that flowing a liquid containing molecules, molecular groups, molecular parts and/or cells through a duct which is in contact with a target structure will cause said molecules, molecular groups, molecular parts and/or cells to bind to said target structure. Any non-binding matter can be removed via the second duct aperture. At the same time, the temperature of the object holder will be controlled by the object holder thermostat. Owing to the flowing motion, passing the liquid containing molecules, molecular groups, molecular parts and/or cells over the target structure is a better way of simulating natural systems with short-term interactions than by means of a prior art shaker or a prior art rotating table. A particular advantage of the invention is that it allows an interruption of metabolic processes at any time by decreasing the temperature of the object holder by means of the object holder thermostat. In doing so, the temperature of the object holder will be 2-10° C., in particular 4° C.
  • In an advantageous embodiment of the invention, the duct is formed by the object holder and paraffin-like sheet material. This allows the duct to widen, if necessary, preventing excessive pressure build-up within said duct.
  • In yet another advantageous embodiment of the invention, the discharged liquid will be collected in a vessel, thus preventing a loss of liquid which has already passed the duct, which liquid may be difficult and/or expensive to prepare.
  • In another advantageous embodiment of the invention, the temperature of the vessel will be cooled by a vessel thermostat, thus preventing any metabolic processes from occurring within said vessel and allowing the liquid or its ingredients to be used again.
  • A method of the invention for binding molecules, molecular groups, molecular parts and/or cells contained in a liquid to target structures comprises the following steps: (a) passing liquid through a duct and over an object holder carrying a target structure firmly held therein, (b) removing any non-binding matter via a second duct aperture and collecting such matter in a vessel, (c) cooling said object holder by means of an object holder thermostat, and (d) fixing the molecules, molecular groups, molecular parts and/or cells adhering to the object holder.
  • In yet another advantageous embodiment of the invention, the device is used in an automated method for determining molecular classes, molecular groups, molecular parts in a solid or liquid object according to U.S. patent application Ser. No. 09/353,942, the entire specification of which is incorporated herein by this reference. This will allow identification and characterization of the binding partners. It will be possible at the same time to identify and characterize the molecular classes, molecular groups and/or molecular parts required for the binding process. Such application will be advantageous in numerous areas of chemistry, biology, biochemistry and especially medicine. This will not only open up new possible ways of diagnosing, but will also provide a new test system for therapeutic approaches on a molecular level.
  • Further details, features and advantages of the invention will ensue from the description, which follows, of an embodiment illustrated in the drawings, of which:
  • FIG. 1 a is a top view of an object holder of the device of the invention;
  • FIG. 1 b is a cross-sectional view of the object holder of FIG. 1 a;
  • FIG. 2 a is a schematic lateral view of the device of the invention; and
  • FIG. 2 b is a detailed view of an element of the device of the invention.
  • FIG. 1 a is a top view of an object holder 10 of the device for binding molecules, molecular groups, molecular parts and/or cells, whereas FIG. 1 b is a cross-sectional view of the object holder 10.
  • It can be seen that a target structure 12 has been detachably mounted on said object holder 10 and contacts a duct 14 defined by said object holder 10, two paraffin-sheet strips 20 and a continuous paraffin-sheet layer 22. Two aluminum rails 24 are mounted on said paraffin-sheet layer 22 whose surface areas are similar to that of said paraffin-sheet strips 20 underneath them. Furthermore, it may be gathered from this figure that duct 14 has first and second duct apertures 16, 18 for inlet and outlet, resp., of liquid 62. Liquid 62 may be discharged by means of a plunger mechanism 58, a pump (not shown), or under the influence of gravity and by means of a pump (not shown), or under the influence of gravity alone.
  • FIG. 2 a is a schematic lateral view of the device for binding molecules, molecular groups, molecular parts and/or cells, with said object holder 10, including paraffin-sheet strips 20, paraffin-sheet layer 22, aluminum rails 24, a hollow needle 60 and said liquid 62, being additionally shown in detail in FIG. 2 b.
  • These illustrations show that—besides the elements mentioned above—the device includes an object holder thermostat 26 comprising a cooling plate 28, made of aluminum, a first Peltier element 30, a first cooling element 32 and a first fan 34. Said device is mounted on a post 52 with clamping joint 54 in such a way that the angle between the mounted object holder 10 and a basic plate 64 is approx. 20-70°. Object holder 10 is firmly pressed onto object holder thermostat 26 by a pressure plate with a central aperture 36 which rests on aluminum rails 24. Sufficient pressure is ensured by way of springs 38.
  • Liquid 62 is introduced into the first duct aperture 16 by means of a suture 58 detachably mounted by means of a suture support 56, and a hollow needle. Under the influence of gravity, liquid 62 will thus flow through duct 14 and contact target structure 12, allowing the desired and predetermined ingredients of liquid 62 to bind to target structure 12. Finally, liquid 62 will reach the second duct aperture 18, exit duct 14 and drip into a vessel 40 surrounded by a vessel thermostat 42. Said vessel thermostat 42 comprises a vessel support 44, made of copper, a second Peltier element 46, a second cooling element 48 and a second fan 50.
  • Once all of said liquid 62 (approx. 1 ml) has passed through said duct 14, object holder thermostat 26 and vessel thermostat 42 will cool said vessel 40 and said object holder 10 down to 4° C. so as to stop any metabolic activity.
  • Liquid 62 may contain lymphocytes. Target structure 12 is a tissue section or a membrane coated with molecules or molecular combinations.

Claims (2)

1-13. (canceled)
14. A method for binding molecules, molecular groups, molecular parts and/or cells contained in a liquid to target structures wherein said method comprises the following steps:
a. passing liquid through a duct and over an object holder with a target structure firmly held therein,
b. removing any non-binding matter via a second aperture of said duct and collecting said matter in a vessel,
c. cooling said object holder by means of an object holder thermostat, and
d. fixing the molecules, molecular groups, molecular parts and/or cells binding to said object holder.
US11/089,304 1999-07-14 2005-03-24 Device for binding molecules, molecular groups, molecular parts and/or cells Abandoned US20050170426A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US11/089,304 US20050170426A1 (en) 1999-07-14 2005-03-24 Device for binding molecules, molecular groups, molecular parts and/or cells

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
DE19932958.3 1999-07-14
DE19932958A DE19932958C2 (en) 1999-07-14 1999-07-14 Device for binding molecules, groups of molecules, parts of molecules and / or cells
US09/613,964 US6875579B1 (en) 1999-07-14 2000-07-11 Device for binding molecules, molecular groups, molecular parts and/or cells
US11/089,304 US20050170426A1 (en) 1999-07-14 2005-03-24 Device for binding molecules, molecular groups, molecular parts and/or cells

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US09/613,964 Continuation US6875579B1 (en) 1999-07-14 2000-07-11 Device for binding molecules, molecular groups, molecular parts and/or cells

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US11/089,304 Abandoned US20050170426A1 (en) 1999-07-14 2005-03-24 Device for binding molecules, molecular groups, molecular parts and/or cells

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EP (1) EP1069431B1 (en)
JP (1) JP2001078747A (en)
AT (1) ATE256288T1 (en)
DE (2) DE19932958C2 (en)
ES (1) ES2212944T3 (en)

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US20090061756A1 (en) * 2007-08-30 2009-03-05 Mark Germagian System and method for cooling electronic equipment

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DE10251338B4 (en) * 2002-11-05 2008-05-21 Intavis Bioanalytical Instruments Ag Device for carrying out staining and hybridization reactions
CA2674140C (en) 2007-01-05 2018-05-15 University Of Zurich Method of providing disease-specific binding molecules and targets

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JP2001078747A (en) 2001-03-27
ATE256288T1 (en) 2003-12-15
DE19932958A1 (en) 2001-02-15
DE19932958C2 (en) 2003-08-07
EP1069431A2 (en) 2001-01-17
US6875579B1 (en) 2005-04-05
ES2212944T3 (en) 2004-08-16
DE50004699D1 (en) 2004-01-22
EP1069431B1 (en) 2003-12-10
EP1069431A3 (en) 2001-08-22

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