A Microwell Array Platform for Picoliter Membrane Protein Assays

被引:11
作者
Binkert, Andreas [1 ]
Studer, Philipp [1 ]
Voeroes, Janos [1 ]
机构
[1] ETH, Inst Biomed Engn, Lab Biosensors & Bioelect, CH-8092 Zurich, Switzerland
关键词
arrays; biosensors; lipid bilayers; membranes; protein screening; SUPPORTED LIPID-BILAYERS; MICROARRAY TECHNOLOGY; ADSORPTION; PROTEOMICS; STABILITY; KINETICS; CELLS;
D O I
10.1002/smll.200801289
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A novel microwell chip is developed that can be used to detect protein binding in a liquid environment, together with a liquid handling system that allows the performance of assays with picoliter volumes. A PDMS well structure is cast on a planar optical waveguide, providing reaction containers combined with a high-sensitivity fluorescence readout system. Individual wells of the array can be addressed, filled, and rinsed using a contact-mode pin and ring spotter. This allows for immunoassays in a heavily multiplexed way, as all steps of the assay can be individually chosen per well. An array density of over 1000 wells cm(-2) is used for the current experiments. The wells provide a protected liquid environment in which the handling of proteins in their natural state is possible, thus maintaining their activity. The membrane protein annexin V is chosen as a model protein to demonstrate the current possibilities. Annexin V binds to phosphatidylserine (PS) head groups of lipids in a Ca2+-dependent manner and is often chosen as a marker for cell apoptosis. Lipid vesicles with and without PS are spotted in individual wells and spontaneously formed a planar lipid bilayer on the bottom of the buffer-filled wells. Annexin V can be used to distinguish between wells containing PS groups previously incorporated in the membrane patches and reference wells without PS head groups. Also, the dependence on the calcium concentration can be shown. Fluorescence readout of the assays is performed using a highly sensitive system based on a planar optical waveguide.
引用
收藏
页码:1070 / 1077
页数:8
相关论文
共 33 条
[1]   Progress in protein and antibody microarray technology [J].
Angenendt, P .
DRUG DISCOVERY TODAY, 2005, 10 (07) :503-511
[2]   Optical microarray biosensing techniques [J].
Bally, Marta ;
Halter, Martin ;
Voeroes, Janos ;
Grandin, H. Michelle .
SURFACE AND INTERFACE ANALYSIS, 2006, 38 (11) :1442-1458
[3]   ALLOGENEIC STIMULATION OF CYTO-TOXIC T-CELLS BY SUPPORTED PLANAR MEMBRANES [J].
BRIAN, AA ;
MCCONNELL, HM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (19) :6159-6163
[4]   THE ANNEXIN FAMILY OF CALCIUM-BINDING PROTEINS [J].
BURGOYNE, RD ;
GEISOW, MJ .
CELL CALCIUM, 1989, 10 (01) :1-10
[5]   Imaging large arrays of supported lipid bilayers with a macroscope [J].
Castellana, Edward T. ;
Cremer, Paul S. .
BIOINTERPHASES, 2007, 2 (02) :57-63
[6]   Solid supported lipid bilayers: From biophysical studies to sensor design [J].
Castellana, Edward T. ;
Cremer, Paul S. .
SURFACE SCIENCE REPORTS, 2006, 61 (10) :429-444
[7]   Electrochemical analysis in picoliter microvials [J].
Clark, RA ;
Hietpas, PB ;
Ewing, AG .
ANALYTICAL CHEMISTRY, 1997, 69 (02) :259-263
[8]   Creating spatially addressed arrays of planar supported fluid phospholipid membranes [J].
Cremer, PS ;
Yang, TL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (35) :8130-8131
[9]   Stability of molded polydimethylsiloxane microstructures [J].
Delamarche, E ;
Schmid, H ;
Michel, B ;
Biebuyck, H .
ADVANCED MATERIALS, 1997, 9 (09) :741-746
[10]   Membrane protein microarrays [J].
Fang, Y ;
Frutos, AG ;
Lahiri, J .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (11) :2394-2395