» Articles » PMID: 20957050

µFBI: a Microfluidic Bead-based Immunoassay for Multiplexed Detection of Proteins from a µL Sample Volume

Overview
Journal PLoS One
Date 2010 Oct 20
PMID 20957050
Citations 12
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Over the last ten years, miniaturized multiplexed immunoassays have become robust, reliable research tools that enable researchers to simultaneously determine a multitude of parameters. Among the numerous analytical protein arrays available, bead-based assay systems have evolved into a key technology that enables the quantitative protein profiling of biological samples whilst requiring only a minimal amount of sample material.

Methodology/principal Findings: A microfluidic bead-based immunoassay, µFBI, was developed to perform bead-based multiplexed sandwich immunoassays in a capillary. This setup allows the simultaneous detection of several parameters and only requires 200 ng of tissue lysate in a 1 µL assay volume. In addition, only 1 µL of detection antibodies and 1 µL of the reporter molecule Streptavidin-Phycoerythrin were required. The µFBI was used to compare the expression of seven receptor tyrosine kinases and their degree of tyrosine phosphorylation in breast cancer tissue and in normal tissue lysates. The total amount of HER-2, as well the degree of tyrosine phosphorylation was much higher in breast cancer tissue than in normal tissue. µFBI and a standard bead-based assay led to identical protein expression data. Moreover, it was possible to reduce the quantity of sample material required by a factor of 100 and the quantity of reagents by a factor of 30.

Conclusions/significance: The µFBI, microfluidic bead-based immunoassay, allows the analysis of multiple parameters from a very small amount of sample material, such as tumor biopsies or tissue sections.

Citing Articles

Highly Sensitive Multiplex Detection of Molecular Biomarkers Using Hybridization Chain Reaction in an Encoded Particle Microfluidic Platform.

Rutten I, Daems D, Leirs K, Lammertyn J Biosensors (Basel). 2023; 13(1).

PMID: 36671935 PMC: 9856145. DOI: 10.3390/bios13010100.


Micromotor-Based Biosensing Using Directed Transport of Functionalized Beads.

Park S, Yossifon G ACS Sens. 2020; 5(4):936-942.

PMID: 32141739 PMC: 7467824. DOI: 10.1021/acssensors.9b02041.


High-Throughput Incubation and Quantification of Agglutination Assays in a Microfluidic System.

Castro D, Conchouso D, Kodzius R, Arevalo A, Foulds I Genes (Basel). 2018; 9(6).

PMID: 29867050 PMC: 6027479. DOI: 10.3390/genes9060281.


Single-Cell, Multiplexed Protein Detection of Rare Tumor Cells Based on a Beads-on-Barcode Antibody Microarray.

Yang L, Wang Z, Deng Y, Li Y, Wei W, Shi Q Anal Chem. 2016; 88(22):11077-11083.

PMID: 27644430 PMC: 5519775. DOI: 10.1021/acs.analchem.6b03086.


Protein Microarrays with Novel Microfluidic Methods: Current Advances.

Dixit C, Aguirre G Microarrays (Basel). 2016; 3(3):180-202.

PMID: 27600343 PMC: 4996363. DOI: 10.3390/microarrays3030180.


References
1.
Ramachandran N, Raphael J, Hainsworth E, Demirkan G, Fuentes M, Rolfs A . Next-generation high-density self-assembling functional protein arrays. Nat Methods. 2008; 5(6):535-8. PMC: 3070491. DOI: 10.1038/nmeth.1210. View

2.
Templin M, Stoll D, Bachmann J, Joos T . Protein microarrays and multiplexed sandwich immunoassays: what beats the beads?. Comb Chem High Throughput Screen. 2004; 7(3):223-9. DOI: 10.2174/1386207043328814. View

3.
Paczesny S, Krijanovski O, Braun T, Choi S, Clouthier S, Kuick R . A biomarker panel for acute graft-versus-host disease. Blood. 2008; 113(2):273-8. PMC: 2615645. DOI: 10.1182/blood-2008-07-167098. View

4.
Yu X, Schneiderhan-Marra N, Joos T . Protein microarrays for personalized medicine. Clin Chem. 2010; 56(3):376-87. PMC: 7108201. DOI: 10.1373/clinchem.2009.137158. View

5.
Baselga J, Swain S . Novel anticancer targets: revisiting ERBB2 and discovering ERBB3. Nat Rev Cancer. 2009; 9(7):463-75. DOI: 10.1038/nrc2656. View