Histone H4, acetylated (Lys8)

Blue Ice

2, 0096

Supplied as a solution in sterile deionized water.

Sequence: SGRGKGG[AcK]GLGKGGAKRHR-C, which corresponds to the N terminal sequence of histone H4 acetylated at position 8 plus a C terminal cysteine.

Application(s):
May be used to measure histone acetyltransferase (HAT) activity. May be acetylated by HAT on lysines at position 5, 12 and 16. May be used to determine the preferred acetylation site by any particular HAT that acetylates histone H4, when used with peptides of identical sequence but differing acetylated lysine residues.

Dot Blot: Used as a standard to assess the specificity of anti-acetyl histone antibodies for acetyl lysine 8 of Histone H4.

Autoantibodies to histone antigens have been described in patients with idiopathic and drug-induced SLE, rheumatoid arthritis, and other conditions. The presence of autoantibodies to histones are frequently found in several rheumatic disorders (1). In one study, the predominant responses to histones in SLE sera were to H1, H2b, and H3. Marked elevations of binding occurred to H1 and H2b in 33% of patients, while 25% showed higher binding to H3 (2). The same study showed the highest anti-histone reactivity to be in patients with rheumatoid arthritis with vasculitis, while the highest reactivity in SLE sera was in those patients with a history of photosensitivity (3).

In diploid eukaryotic cells, the chromatin fibers are about 20nM in diameter. They consist of two major components in equal amounts, DNA and basic proteins called histones. The histones are a group of water and dilute acid soluble basic proteins found associated with DNA in chromosomes. They are characterized by relatively high levels of lysine and arginine. Although histones are classified into a limited number of types of fractions (see below) with each particular fraction having a fundamentally distinct amino acid composition and sequence, numerous subfractions are observed due to the acetylation, methylation, and phosphorylation of various amino acid residues. Microheterogeneity or alteration of structure is dynamic such that the histones of a single cell type are found to vary during development. They are believed to play a role in gene activity and cellular metabolism.

Histones are believed to be regularly arranged in the deep groove of the DNA helix. The recurring positive charges of the histones form electrostatic associations with the negatively charged phosphate groups of DNA making the DNA more stable and flexible. This allows for the supercoiling of the chromatin fibers.

With the exception of H1, the primary structures of the calf thymus histones have been determined. Comparisons with the structures for histones from other sources indicate that the histones rank among the most highly conserved (low mutation rate) proteins in nature.

Molecular Weights of Histones:
Lysine Rich (H1, f1): ~ 21, 500
Slightly Lysine Rich (H2a, f2a2): 14, 004
Slightly Lysine Rich (H2b, f2b): 13, 774
Arginine Rich (H3, f3): 15, 324
Arginine Rich (H4, f2a1): 11, 282