WO1999019276A3 - Molecular compounds having complementary surfaces to targets - Google Patents

Molecular compounds having complementary surfaces to targets Download PDF

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Publication number
WO1999019276A3
WO1999019276A3 PCT/US1998/021804 US9821804W WO9919276A3 WO 1999019276 A3 WO1999019276 A3 WO 1999019276A3 US 9821804 W US9821804 W US 9821804W WO 9919276 A3 WO9919276 A3 WO 9919276A3
Authority
WO
WIPO (PCT)
Prior art keywords
target
targets
spcs
spc
network
Prior art date
Application number
PCT/US1998/021804
Other languages
French (fr)
Other versions
WO1999019276A2 (en
Inventor
David S Soane
Stephen E Barry
Andrew Goodwin
David A Offord
Michael G Perrot
Original Assignee
Alnis Llc
David S Soane
Stephen E Barry
Andrew Goodwin
David A Offord
Michael G Perrot
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Alnis Llc, David S Soane, Stephen E Barry, Andrew Goodwin, David A Offord, Michael G Perrot filed Critical Alnis Llc
Priority to AU13610/99A priority Critical patent/AU1361099A/en
Priority to EP98957326A priority patent/EP1025066A2/en
Publication of WO1999019276A2 publication Critical patent/WO1999019276A2/en
Publication of WO1999019276A3 publication Critical patent/WO1999019276A3/en

Links

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/68Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08BPOLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B37/00Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
    • C08B37/0006Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid
    • C08B37/0009Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid alpha-D-Glucans, e.g. polydextrose, alternan, glycogen; (alpha-1,4)(alpha-1,6)-D-Glucans; (alpha-1,3)(alpha-1,4)-D-Glucans, e.g. isolichenan or nigeran; (alpha-1,4)-D-Glucans; (alpha-1,3)-D-Glucans, e.g. pseudonigeran; Derivatives thereof
    • C08B37/0021Dextran, i.e. (alpha-1,4)-D-glucan; Derivatives thereof, e.g. Sephadex, i.e. crosslinked dextran
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G83/00Macromolecular compounds not provided for in groups C08G2/00 - C08G81/00
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53Immunoassay; Biospecific binding assay; Materials therefor
    • G01N33/531Production of immunochemical test materials
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2333/00Assays involving biological materials from specific organisms or of a specific nature
    • G01N2333/90Enzymes; Proenzymes
    • G01N2333/914Hydrolases (3)
    • G01N2333/948Hydrolases (3) acting on peptide bonds (3.4)
    • G01N2333/976Trypsin; Chymotrypsin
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2400/00Assays, e.g. immunoassays or enzyme assays, involving carbohydrates
    • G01N2400/10Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
    • G01N2400/12Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar
    • G01N2400/14Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar alpha-D-Glucans, i.e. having alpha 1,n (n=3,4,6) linkages between saccharide units, e.g. pullulan
    • G01N2400/22Dextran
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2600/00Assays involving molecular imprinted polymers/polymers created around a molecular template

Abstract

Synthetic polymer complements (SPCs) are provided, as well as methods for their synthesis and use. The SPCs may have surfaces that include functional groups that are complementary to surface sites of targets such as nanostructures or macromolecular targets, and may be capable of specifically interacting with such targets. The positions of the functional groups in one embodiment are stabilized by a polymer network. The SPCs are formed by contacting the target with a set of monomers which self-assemble on the target, and then are polymerized into a network to form the synthetic polymer complement. At least a portion of the surface of the resulting SPC thus may include an imprint of the target. The complex of the SPC and the target may be the desired product. Alternatively, the target is released, for example, by controllably expanding and contracting the cross-linked network. The SPC is isolated and used in many applications.
PCT/US1998/021804 1997-10-14 1998-10-14 Molecular compounds having complementary surfaces to targets WO1999019276A2 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
AU13610/99A AU1361099A (en) 1997-10-14 1998-10-14 Molecular compounds having complementary surfaces to targets and methods for thesynthesis and use thereof
EP98957326A EP1025066A2 (en) 1997-10-14 1998-10-14 Molecular compounds having complementary surfaces to targets

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US6180597P 1997-10-14 1997-10-14
US60/061,805 1997-10-14
US09/172,921 1998-10-09
US17292198A 1998-10-14 1998-10-14

Publications (2)

Publication Number Publication Date
WO1999019276A2 WO1999019276A2 (en) 1999-04-22
WO1999019276A3 true WO1999019276A3 (en) 1999-08-19

Family

ID=26741507

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1998/021804 WO1999019276A2 (en) 1997-10-14 1998-10-14 Molecular compounds having complementary surfaces to targets

Country Status (3)

Country Link
EP (1) EP1025066A2 (en)
AU (1) AU1361099A (en)
WO (1) WO1999019276A2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP7296636B2 (en) 2018-07-20 2023-06-23 藤本化学製品株式会社 Alkoxyphenyl derivative, protected nucleoside and protected nucleotide, method for producing oligonucleotide, and method for removing substituent

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6380336B1 (en) 1998-03-24 2002-04-30 Nano-Tex, Llc Copolymers and oil-and water-repellent compositions containing them
US6217901B1 (en) 1999-05-25 2001-04-17 Alnis, Llc Liposome-assisted synthesis of polymeric nanoparticles
US6844028B2 (en) * 2001-06-26 2005-01-18 Accelr8 Technology Corporation Functional surface coating
CA2470524A1 (en) * 2001-12-21 2003-07-24 David S. Soane Use of oligomers and polymers for drug solublization, stabilization, and delivery
WO2005118877A2 (en) * 2004-06-02 2005-12-15 Vicus Bioscience, Llc Producing, cataloging and classifying sequence tags
WO2009064245A1 (en) * 2007-11-12 2009-05-22 Mip Technologies Ab Imprinted polymers with affinity for phosphorylated peptides and proteins
EP2386061A4 (en) * 2009-01-12 2012-07-18 Univ California Imprinted polymer nanoparticles
CN104897846B (en) * 2015-06-23 2016-08-17 江南大学 A kind of based on the alkaline phosphatase activities detection method being formed in situ non-photoactive nanoparticles material simulation enzyme
JP6770553B2 (en) * 2018-07-20 2020-10-14 藤本化学製品株式会社 Alkoxyphenyl derivative, nucleoside protector and nucleotide protector, oligonucleotide production method, and substituent removal method

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4770906A (en) * 1985-04-19 1988-09-13 The Board Of Regents For The University Of Oklahoma Producing polymeric films from a surfactant template
US5310648A (en) * 1991-02-01 1994-05-10 California Institute Of Technology Composition of matter comprising an imprinted matrix exhibiting selective binding interactions through chelated metals
DE19823432A1 (en) * 1997-09-09 1999-03-11 Thomas Prof Dr Bayerl Molecular imprinting of solid-supported amphiphile layer capable of undergoing reversible phase transition

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4770906A (en) * 1985-04-19 1988-09-13 The Board Of Regents For The University Of Oklahoma Producing polymeric films from a surfactant template
US5310648A (en) * 1991-02-01 1994-05-10 California Institute Of Technology Composition of matter comprising an imprinted matrix exhibiting selective binding interactions through chelated metals
DE19823432A1 (en) * 1997-09-09 1999-03-11 Thomas Prof Dr Bayerl Molecular imprinting of solid-supported amphiphile layer capable of undergoing reversible phase transition

Non-Patent Citations (6)

* Cited by examiner, † Cited by third party
Title
KEMPE M ET AL: "Molecular imprinting used for chiral separations", JOURNAL OF CHROMATOGRAPHY A, vol. 694, no. 1, 3 March 1995 (1995-03-03), pages 3-13, XP004023308 *
M MURATA, S HIJIYA, M MAEDA, M TAKAGI: "Template-Dependent Selectivity in Metal Adsorption on Phosphoric Diester-Carrying Resins Prepared by Surface Template Polymerization Technique", BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, vol. 69, no. 3, 1996, pages 637 - 642, XP002105145 *
N KAMIYA, M GOTO: "Preparation of surfactant-coated lipases utilizing the molecular imprinting technique", JOURNAL OF FERMENTATION AND BIOENGINEERING, vol. 85, no. 2, 1998, pages 237 - 239, XP002105148 *
S A PILETSKY, H S ANDERSSON, I A NICHOLLS: "The rational use of hydrophobic effect-based recognition in molecularly imprinted polymers", JOURNAL OF MOLECULAR RECOGNITION, vol. 11, no. 1-6, 1998, pages 94 - 97, XP002105146 *
WULFF G: "MOLECULAR IMPRINTING IN CROSS-LINKED MATERIALS WITH THE AID OF MOLECULAR TEMPLATES - A WAY TOWARDS ARTIFICIAL ANTIBODIES", ANGEWANDTE CHEMIE. INTERNATIONAL EDITION, vol. 34, no. 17, 15 September 1995 (1995-09-15), pages 1812 - 1832, XP000524863 *
X X ZHU, K BANANA, R YEN: "Pore-size control in cross-linked polymer resins by reverse micellar imprinting", MACROMOLECULES, vol. 30, no. 10, 1997, pages 3031 - 3035, XP002105147 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP7296636B2 (en) 2018-07-20 2023-06-23 藤本化学製品株式会社 Alkoxyphenyl derivative, protected nucleoside and protected nucleotide, method for producing oligonucleotide, and method for removing substituent

Also Published As

Publication number Publication date
AU1361099A (en) 1999-05-03
WO1999019276A2 (en) 1999-04-22
EP1025066A2 (en) 2000-08-09

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