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AVAILABLE CHIPS AND
COUPLING CHEMISTRIES:
1) CM5 (Carboxymethyl dextran surface):
This chip is the most commonly used. The following types of coupling
chemistries are available for activating this surface:
AMINE. Direct linkage via
primary amines on the protein/peptide. Surface activation is by EDC
(N-ethyl-N'-(3-dimethyl aminopropyl)-carbodiimide hydrochloride), and NHS
(N-hydroxysuccinimide).
SURFACE
THIOL. Direct
linkage via thiols generated on the chip surface. Surface activation is by
EDC/NHS followed by preparation with Cystamine and DTT.
LIGAND
THIOL. Direct linkage via thiols on the protein/peptide. Surface
activation is by EDC/NHS followed by preparation with PDEA
(pyridinyldithioethaneamine hydrochloride).
ALDEHYDE. Direct linkage via
carbohydrate on the protein/molecule. Surface activation is by EDC/NHS
followed by preparation with hydrazine.
This chip is essentially a "blank"
chip that lacks the carboxymethyl dextran of the CM5 chip. The surface is
composed of hydrophobic alkanethiol goups. This chip can be used to mimic
conditions of an ELISA (hydrophobic adsorption of protein), or to lay down
lipid monolayers of various compositions. The latter can be used to study
protein-lipid interactions or protein-protein interactions using a
membrane-associated protein/receptor.
This chip is a prepared CM5 chip with streptavidin coupled to the surface. This
surface can be used to "capture" any molecule that has been labeled
with biotin (protein, peptide, DNA, oligos, etc.).
4) NTA (Nickel Chelation surface):
This chip has been prepared with a nickel-chelating agent, and can thus be used
to "capture" proteins/peptides containing His tags.
5) Pioneer chip L1:
This chip is useful for the rapid and
reproducible capture of liposomes.
6) Pioneer chip B1:
This chip has a shortened dextran matrix and is useful with analytes that show
a high degree of non-specific binding to the CM-5 chip.