Active Motif offers a wide variety of recombinant histones that include site- and degree-specific modifications such as methylation, acetylation and phosphorylation. The combination of histone post-translational modifications form the basis of the “histone code” that serves to regulate a variety of nuclear functions, including interactions with chromatin-associated proteins, nucleosome remodeling, transcriptional regulation, replication and DNA repair. Each recombinant histone is prepared using one of two patented technologies: Expressed Protein Ligation (EPL) or Methylated Lysine Analog (MLA). We also offer a subset of our histone H3 proteins that have been biotinylated for use in FRET assays and other capture techniques.
With our MLA technology, methylated histones are generated via a chemical alkylation reaction that introduces a methyl-lysine analog at the desired lysine location, giving us precise control over the site and degree of methylation. Alternatively, the EPL technology can be used to generate methylated, acetylated and phosphorylated histones. Using EPL, the histone globular domain is ligated to a peptide that contains the N-terminal histone tail with the desired modifications. This ligation reaction maintains the native histone bonds. Both methods produce proteins that are validated to be over 98% pure. For more information on the EPL and MLA technologies, click on the EPL and MLA Technologies tab below.
Active Motif also offers a number of biotinylated recombinant histone H3 proteins. Biotin is linked either to unmodified or modified recombinant H3 protein at its N-terminus via a carbon linker. The addition of biotin enables the recombinant histones to be used as a substrate for capture of protein binding interactions. Biotinylated histone H3 proteins are also ideal substrates for homogenous FRET assays. Simply incubate the recombinant histone with the enzyme of interest and detect using streptavidin-coated donor beads and antibody-conjugated acceptor beads.
A complete list of recombinant histones is shown below. Click on the protein name to see complete information.
|Name||Expressed In||Format||Cat No.||Price|
|Recombinant Histone H1||E. coli||100 µg||81126||¥880||Buy|
|Recombinant Histone H1.2||E. coli||50 µg||81252||¥1,240||Buy|
|Recombinant Histone H2A (Human)||E. coli||100 µg||31490||¥880||Buy|
|Recombinant Histone H2A/H2B dimer||E. coli||100 µg||81167||¥3,280||Buy|
|Recombinant Histone H2A.Z||Synthetic||25 µg||31293||Discontinued|
|Recombinant Histone H2A.Z/H2B dimer||E. coli||100 µg||81168||¥3,360||Buy|
|Recombinant Histone H2B (Human)||E. coli||100 µg||31492||¥880||Buy|
|Recombinant Histone TH2B||E. coli||100 µg||31577||¥1,240||Buy|
|Recombinant Histone H2BFWT||E. coli||100 µg||31578||¥1,240||Buy|
|Recombinant Histone H3 (C110A)||E. coli||100 µg||31207||¥5,330||Buy|
|Histone Analysis Products Profile|
|Histone Modifications Guide|
|Recombinant Proteins for Epigenetics Research|
|Epigenetics Products and Services|
The ability to alter protein structure through the introduction of synthetic modifications is a powerful technique that can be utilized to dissect protein function and to facilitate the generation of research tools or therapeutic reagents. Chemical synthesis of peptides is a technically demanding process and also restricts the size of the generated protein. Therefore, a more robust technique is required to generate large modified proteins, such as histones.
Current methods used for constructing modified recombinant histones include solid phase peptide synthesis (SPPS), reductive alkylation and semisynthetic methods that utilize transferases to catalyze the transfer of modified groups to specified residues. However these methods have their disadvantages, including:
- Size limitation of the synthesized protein
- The availability of the transferase enzyme
- Variability in the degree of modifications catalyzed by the reaction
- Heterogeneity in the specificity of the enzyme
EPL and MLA Technologies
To overcome these limitations, Active Motif’s recombinant histones are engineered using one of two patented technologies: Expressed Protein Ligation (EPL) or Methylated Lysine Analog (MLA).
EPL is a semisynthetic method in which an expressed protein (rather than a synthesized peptide with limited fragment size) containing an unprotected C-terminal thioester is ligated to a peptide containing an N-terminal cysteine via a chemoselective reaction. The reaction, known as ‘native chemical ligation,’ preserves the native amine bond. In the case of recombinant histones, this involves the ligation of a histone tail containing the site-specific modification to the globular histone globular domain. Along with preserving the natural protein structure, this method allows for the engineering of large synthetic proteins and permits incorporation of a broad range of histone modifications found in nature.
Click on image to enlarge size.
Figure 1: Generation of modified recombinant histones using the EPL method.
Using the alternative MLA technology, methylated histones are generated via a chemical alkylation reaction that substitutes a methylated analog of lysine, aminoethylcysteine, for the existing lysine at the desired residue. Aminoethylcysteine is structurally and chemically similar to lysine, though it contains an ethylamine substitution in place of the lysine ϒ-methylene. The lysine analogs can be chemically treated for engineering of modified histones to provide precise control over the site and degree of methylation. Studies demonstrate that modified histones engineered using the MLA technique show functional similarity to their natural counterparts.
Click on image to enlarge size.
Figure 2: Comparison of the chemical structures of lysine and methyl-lysine analogs.
Figure 3: Comparison of the performance of histone substrates in a histone demethylase assay reveal recombinant histone H3K4me2 protein (MLA) more closely mimics native histone substrates.
- Lin, J.C. et al. (2007) Cancer Cell, 12: 432-444.
- Muir, T.W. (2003) Annu Rev Biochem, 72: 249-289