MicroSurfaces, Inc.

Home

News

Order

Products

Service

Distributors

About us

Contact us



The ZeroBkg® Technology

Read the applications notes: | PEG | Biotin | Polylysine |Silane | NHS | Chelated Cu2+ | Click Chemistry | Maleimide | SPR | Cell Membranes |

Read recent Publications from authors using our surfaces.


Proteins tend to adsorb nonspecifically to most solid surfaces. This is because a protein molecule has various hydrophobic domains, charged sites, and hydrogen bond donor/acceptor groups and can bind strongly with hydrophobic surfaces, oppositely charged sites, and hydrogen bond acceptor/donor groups. Strong non-specific adsorption is a problem both at the probe immobilization stage and at the probe-target interaction stage: a) excessive interaction between an immobilized protein molecule and a solid surface can result in the disruption of its 3D structure and eventually denaturation; and b) non-specific adsorption of target protein molecules during assay leads to background signal. A successful strategy to circumvent the nonspecific adsorption problem is to start with an inert coating which is intrinsically repulsive to protein adsorption. The coating can be activated for the selective immobilization of probe protein molecules while the surrounding surface remains repulsive.

We have successfully developed a proprietary technology which allows us to coat glass, silicon wafer, quartz, & other substrates with a robust, high density layer of poly-ethyleneglycol (PEG) brush. The density of PEG functionality on the surface is orders of magnitude higher than those from the conventional silane coupling chemistry. The PEG coating is intrinsically inert towards the adsorption of proteins, cells and other biomolecules, thus providing a zero-background starting surface in a variety of biomedical experiments. We have also developed various surface conjugation chemistry to allow user to immobilize a wide variety of biomolecues on the otherwise zero background PEG brush. Available funcitonalities include -NHS leaving groups for covalent attachment to -NH2 functional group, biotin for conjugation with the biotin/avidin chemistry, chelated metal ions for binding to poly-histidine tags, alkyne for specific interaction with azide (i.e., Click Chemistry), and maleimide for linking to -SH groups.

These coatings are available on standard microscope slides, coverslips, silicon wafers. We also provide customer coating service for specific customer samples. Our customers have successfully applied these PEG surfaces for a range of applications, including protein sensors, protein microarrays, single molecule spectroscopy, biological atomic force microscopy and other biophysical studies.

PEG brush surfaces
Click on an image to read the specific application note.

Copy Right © 2010 Athena Guo. All rights reserved.

Read about our FluidicArray Technology Here!

1 West Forest Ave, Englewood, NJ 07631, USA
Phone: (201) 408-5596: Fax: (201) 408-5797; E-mail: contact

NHS surfaceImmobilizing poly-HIS tagged proteinsbiotin surfacemaleimide surfacesurface click chemistry