Description
Ni-NTA silica combines Ni-NTA with a macroporous silica support material optimized to suppress nonspecific hydrophobic interactions. Ni-NTA Spin Columns (His-protein purification spin columns) in the Ni-NTA Spin Kit and available separately provide Ni-NTA silica in a convenient microspin format for easy preparation of multiple samples in parallel. They provide a simple method for functional screening of engineered proteins, selection of clones expressing full-length translation products and comparison of expression levels. Each spin column can purify up to 300 µg of His-tagged protein. Like all Ni-NTA matrices, Ni-NTA spin columns can be used for one-step protein purification under native or denaturing conditions. The Ni-NTA Spin Kit is a complete kit for spin purification of His-tagged proteins. It can be automated on the QIAcube Connect (see image "QIAcube Connect").
Ni-NTA Spin Columns (His-protein purification spin columns), also included in the Ni-NTA Spin Kit, allow reproducible fast automated purification (see figure “Reproducible automated purification”) at different expression levels (see figure “Purification at different expression levels”).
The QIA express Ni-NTA Protein Purification System, including the Ni-NTA Spin Columns and Ni-NTA Spin Kit, is based on the remarkable selectivity of patented Ni-NTA (nickel-nitrilotriacetic acid) resin for proteins containing an affinity tag of six or more histidine residues – the His tag. This technology allows one-step purification of almost any His-tagged protein from any expression system under native or denaturing conditions. NTA, which has four chelation sites for nickel ions, binds nickel more tightly than metal-chelating purification systems that only have three sites available for interaction with metal ions. The extra chelation site prevents nickel-ion leaching and results in a greater binding capacity and protein preparations with higher purity than those obtained using other metal-chelating purification systems. The QIA express system can be used to purify His-tagged proteins from any expression system including baculovirus, mammalian cells, yeast and bacteria.
The purification of His-tagged proteins consists of 4 steps: cell lysis, binding, washing and elution (see figure “Ni-NTA Spin Column purification with the Ni-NTA protein purification system”). Purification of recombinant proteins using the QIA express system does not depend on the 3-dimensional structure of the protein or His tag. This allows one-step protein purification under either native or denaturing conditions, from dilute solutions and crude lysates. Up to 600 μl of a cell lysate are loaded onto a Ni-NTA spin column. A quick 2-minute spin binds the tagged protein to Ni-NTA silica, while most of the untagged proteins flow through. After a wash step, purified protein is eluted under mild conditions (such as pH reduction to 5.9, or addition of 100-500 mM imidazole) in a volume of 100-300 μl. Removal of the His tag is usually unnecessary since it is small and rarely immunogenic. The purified protein is ready for immediate use. Proteins can be purified from multiple small-scale expression cultures in around 30 minutes (manual procedure) or approximately 60 minutes (automated QIAcube Connect procedure). Strong denaturants and detergents can be used for efficient solubilization and purification of receptors, membrane proteins and proteins that form inclusion bodies. Reagents that allow efficient removal of nonspecifically binding contaminants can be included in wash buffers (see table). Purified proteins are eluted under mild conditions by adding 100-250 mM imidazole as competitor or by a reduction in pH. Reagents compatible with the Ni-NTA–His interaction: 6 M guanidine HCl 8 M urea 2% Triton X-100 2% Tween 20 1% CHAPS 20 mM β-ME 10 mM DTT 50% glycerol 20% ethanol 2 M NaCl 4 M MgCl2 5 mM CaCl2 ≤20 mM imidazole 20 mM TCEP The reagents listed have been successfully used in concentrations up to those given.
