Parseghian M H, Harris D A, Rishwain D R, Hamkalo B A
Department of Molecular Biology and Biochemistry, University of California, Irvine 92717.
Chromosoma. 1994 Jun;103(3):198-208. doi: 10.1007/BF00368013.
A series of human histone H1 subtype-specific antibodies are described that were generated for localization and functional studies. Since our previous attempts to produce such antibodies against intact subtypes met with limited success, resulting in one antibody against a subtype we have designated H1-3, the approach used in the work presented is based on the production of antibodies against synthetic peptides or peptide fragments encompassing the variant NH2-terminal region of each protein. Subtype-specific antibodies were obtained against synthetic peptides derived from subtypes designated H1-1 and H1-2 and the NH2-terminal fragment from an N-bromosuccinimide digest of H1-4. Antibody specificities were documented in all cases by enzyme-linked immunosorbent and protein immunoblot assays against the purified subtypes as well as immunoblots against whole cell and nuclear extracts. In addition, the in vivo distribution of each antibody was determined by indirect immunofluorescence. H1-1 appears to be distributed in parallel with DNA concentration, similar to the results with an antibody that recognizes all subtypes. However, H1-2 and H1-4 are non-uniformly distributed, exhibiting similar punctate staining patterns. The staining patterns described are different from the pattern described for the distribution of H1-3, suggesting that several subtypes are concentrated in distinct regions of the nucleus and, therefore, may be associated with distinct regions of the genome.
本文描述了一系列针对人类组蛋白H1亚型的特异性抗体,这些抗体用于定位和功能研究。由于我们之前针对完整亚型产生此类抗体的尝试仅取得有限成功,仅得到一种针对我们命名为H1-3的亚型的抗体,因此本文所采用的方法基于针对合成肽或包含每种蛋白质可变NH2末端区域的肽片段产生抗体。针对源自H1-1和H1-2亚型的合成肽以及H1-4经N-溴代琥珀酰亚胺消化后的NH2末端片段获得了亚型特异性抗体。在所有情况下,均通过针对纯化亚型的酶联免疫吸附和蛋白质免疫印迹分析以及针对全细胞和核提取物的免疫印迹来证明抗体的特异性。此外,通过间接免疫荧光确定每种抗体在体内的分布。H1-1的分布似乎与DNA浓度平行,这与识别所有亚型的抗体的结果相似。然而,H1-2和H1-4分布不均匀,呈现出相似的点状染色模式。所描述的染色模式与H1-3分布的模式不同,这表明几种亚型集中在细胞核的不同区域,因此可能与基因组的不同区域相关。