US2010261159A1PendingUtilityA1

Apparatus for assay, synthesis and storage, and methods of manufacture, use, and manipulation thereof

Assignee: HESS ROBERTPriority: Oct 10, 2000Filed: Aug 10, 2006Published: Oct 14, 2010
Est. expiryOct 10, 2020(expired)· nominal 20-yr term from priority
G01N 30/6091B01L 3/5085B01L 3/5025C12M 23/12G01N 30/6095B01J 2219/00389B01J 2219/00659G01N 30/82B01L 13/02B01J 2219/00673B01J 2219/00587B01J 2219/00317B01L 3/50857G01N 30/466B01J 2219/00319B01J 2219/00596B01J 19/0046B01L 3/0244B01J 2219/00648B01J 2219/005B01J 2219/00511B01L 2300/0845B01J 2219/00369B01L 2200/0657B01J 2219/00387B01J 2219/00495B01J 2219/0036B01L 3/50255B01L 3/0262B01J 2219/00351G01N 2030/8417B01L 3/0268C40B 60/14B01J 2219/00423B01J 2219/00653B01J 2219/00479B01J 2219/0043B01J 2219/00585
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Claims

Abstract

The invention features methods of making devices, or “platens”, having a high-density array of through-holes, as well as methods of cleaning and refurbishing the surfaces of the platens. The invention further features methods of making high-density arrays of chemical, biochemical, and biological compounds, having many advantages over conventional, lower-density arrays. The invention includes methods by which many physical, chemical or biological transformations can be implemented in serial or in parallel within each addressable through-hole of the devices. Additionally, the invention includes methods of analyzing the contents of the array, including assaying of physical properties of the samples.

Claims

exact text as granted — not AI-modified
1 - 72 . (canceled) 
     
     
         73 . A cell chip comprising first and second platens, each having a plurality of through-holes, and a porous membrane, wherein the platens are aligned such that the through-holes of the first platen are substantially aligned with the through-holes of the second platen and the membrane is sandwiched in between the two platens. 
     
     
         74 . The cell chip of  claim 73 , wherein the membrane comprises pores that are no more than half the through-hole diameter. 
     
     
         75 . The cell chip of  claim 73 , wherein the membrane comprises pores of between about 0.2-250 μm. 
     
     
         76 - 77 . (canceled) 
     
     
         78 . The cell chip of claim  77 , wherein the membrane comprises aluminum oxide or polycarbonate. 
     
     
         79 - 80 . (canceled) 
     
     
         81 . The cell chip of claim  79 , wherein the polycarbonate is coated with fibronectin, laminin, collagen, or another substrate that supports cell adhesion. 
     
     
         82 . The cell chip of  claim 73 , wherein the platens comprise polystyrene or a metal selected from the group consisting of gold, Tungsten or stainless steel. 
     
     
         83 - 84 . (canceled) 
     
     
         85 . The cell chip of  claim 73 , wherein the chip further comprises a gasket that seals off individual wells. 
     
     
         86 . The cell chip of  claim 85 , wherein the gasket is removable. 
     
     
         87 . The cell chip of  claim 73 , wherein the chip further comprise a hydrophobic compound that prevents lateral diffusion. 
     
     
         88 . (canceled) 
     
     
         89 . The cell chip of  claim 73 , wherein one platen comprises a flexible biocompatible material selected from the group consisting of silicone, polypropylene, or rubber and the other platen is a rigid platen that supports the flexible platen. 
     
     
         90 . (canceled) 
     
     
         91 . The cell chip of  claim 73 , wherein the two platens are attached by raised surfaces on one platen that fit into a recessed surface on the other platen. 
     
     
         92 - 94 . (canceled) 
     
     
         95 . The cell chip of  claim 73 , further comprising a solid support in contact with the first platen. 
     
     
         96 . The cell chip of  claim 95 , wherein the solid support is a microscope slide. 
     
     
         97 . The cell chip of  claim 96 , further comprising a coverslip in contact with the second platen. 
     
     
         98 . The cell chip of  claim 97 , wherein the coverslip, microscope slide, and cell chip are secured together. 
     
     
         99 . A cell chip comprising in order from top to bottom:
 (a) a coverslip in contact with a spacer;   (b) a spacer that separates the covership from a first platen;   (c) a first platen having a plurality of through-holes;   (d) a gasket comprising a plurality of through-holes that provides a seal between the first platent and the membrane;   (e) a porous membrane comprising aluminum oxide and having pores between 0.1 and 1 μm sandwiched between the gasket and the second platen;   (f) a second platent having a plurality of through holes;   (g) a solid support in contact with the second platen.   
     
     
         100 . The cell chip of  claim 99 , wherein the chip further comprises a fastener that holds the various components together. 
     
     
         101 . The cell chip of  claim 99 , wherein the membrane comprises a uniform structure of pores that are 0.2 μm in diameter. 
     
     
         102 . The cell chip of  claim 99 , wherein the platens comprise tungsten, gold, or stainless steel. 
     
     
         103 . A method of culturing a cell on a cell chip, the method comprising:
 (a) providing a cell chip of  claim 73  or  99  comprising cell culture medium;   (b) contacting the porous membrane with a cell; and   (c) incubating the cell under conditions suitable for cell survival.   
     
     
         104 . The method of  claim 103 , wherein the conditions comprise contacting the cell chip a gas permeable liquid. 
     
     
         105 . The method of  claim 104 , wherein the gas permeable liquid is perfluorodecalin. 
     
     
         106 . The method of  claim 104 , wherein the cell chip further comprises a hydrophobic fluid in contact with the cell culture medium, wherein the hydrophobic liquid is selected from the group consisting of perfluorodecalin, silicone oil or and mineral oil 
     
     
         107 . (canceled) 
     
     
         108 . A method of constructing a cell chip of  claim 73  or  99  the method comprising:
 (a) filling a first platen having a plurality of through-holes with cell culture medium;   (b) contacting the first platen with a porous membrane;   (c) contacting the membrane with a second platen having a plurality of through-holes, such that the through-holes are substantially aligned, thereby constructing a cell chip.   
     
     
         109 . The method of  claim 108 , the cell chip further comprising a solid support in contact with the first platen. 
     
     
         110 . The method of  claim 109 , wherein the cell chip further comprises a spacer in contact with the second platen, wherein the spacer is in contact with a cover slip. 
     
     
         111 . The method of  claim 108 , wherein the cell chip further comprises a gasket sandwiched between the first platen. 
     
     
         112 . The method of  claim 108 , wherein the gasket comprises a flexible material or a biocompatible elastomer selected from the group consisting of teflon, silicone, or rubber. 
     
     
         113 - 114 . (canceled) 
     
     
         115 . The method of  claim 108 , wherein the filling is accomplished by placing the first platen on a solid support and centrifuging the platen and solid support. 
     
     
         116 . The method of  claim 108 , wherein the first platen is contacted with a gasket and cell medium is then overlayed on the platen. 
     
     
         117 . A method for identifying an agent having a desired biological activity, the method comprising:
 (a) contacting a cell chip of  claim 73  or  99  comprising a cell with a platen comprising an agent;   (b) contacting the cell with the agent; and   (c) detecting an alteration in the cell, thereby identifying an agent having a desired biological activity.   
     
     
         118 . The method of  claim 117 , wherein the agent is present in cell growth medium, or is contacted with the cell using a slotted pin or syringe, or by adding the cell to a well comprising the agent. 
     
     
         119 . The method of  claim 117 , wherein the agent is a polypeptide, nucleic acid molecule, or small compound. 
     
     
         120 . The method of  claim 117 , wherein the nucleic acid molecule is an siRNA, microRNA, or an aptamer. 
     
     
         121 . The method of  claim 117 , wherein the alteration is an alteration in gene expression, polypeptide expression, cell growth, proliferation or survival, in the intracellular localization of a cellular component, morphological change, or change in motility. 
     
     
         122 . The method of  claim 117 , wherein the alteration is detected in an immunoassay, an enzymatic assay, highthroughput gene expression profiling, reverse transcriptase polymerase chain reaction (RT-PCR), quantitative PCR, real time PCR, methylation, or high content screening (HCS) using quantitative fluorescence microscopy and automated image acquisition. 
     
     
         123 . The method of  claim 117 , wherein the high content screening detects alterations in protein translocation. 
     
     
         124 . The method of  claim 117 , wherein the cell is lysed and the proteins or nucleic acid molecules are bound on a binding surface. 
     
     
         125 . The method of  claim 117 , wherein the binding surface is a weak cationic exchange medium. 
     
     
         126 . The method of  claim 122 , wherein the bound proteins or nucleic acid molecules are analyzed for a characteristic selected from the group consisting of sequence, molecular weight, binding characteristic, and expression level. 
     
     
         127 . The method of  claim 122 , wherein the binding characteristic is detected in an immunoassay or by polypeptide binding.

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