Du Clos T W, Zlock L T, Marnell L
Veterans Administration Medical Center, Albuquerque, New Mexico 87108.
J Biol Chem. 1991 Feb 5;266(4):2167-71.
C-reactive protein (CRP) is an acute phase inflammatory protein in man which binds to phosphocholine, chromatin, histones, and the 70-kDa protein of the U1 small nuclear ribonucleoprotein particle in a calcium-dependent, phosphocholine-inhibitable manner. CRP also binds to other proteins including fibronectin. The determinants involved in CRP binding to these diverse proteins have not been identified. The binding of CRP to histones was examined as these proteins are available in large quantity at high purity and subject to protease digestion with well characterized products. Histone H1 was digested with thrombin and trypsin to produce three distinct fragments, N-terminal, central globular, and C-terminal. CRP was shown only to bind to the C-terminal fragment. Binding to histone H2A was also examined. CRP binding was not diminished by cleavage of the C-terminal fragment but was greatly decreased when the central globular region of H2A was tested. Peptides were prepared to be identical to the N- and C-terminal fragments of H2A. The N-terminal (15 amino acid) fragment of H2A blocked CRP-induced precipitation of phosphocholine-coupled bovine serum albumin and histone H2A, whereas the C-terminal fragment showed no inhibition. Thus we have defined the first reported CRP binding determinant on a protein.
C反应蛋白(CRP)是人体内一种急性期炎症蛋白,它以钙依赖性、磷酸胆碱抑制性方式与磷酸胆碱、染色质、组蛋白以及U1小核核糖核蛋白颗粒的70 kDa蛋白结合。CRP还与包括纤连蛋白在内的其他蛋白质结合。尚未确定参与CRP与这些不同蛋白质结合的决定因素。由于这些蛋白质可大量获得且纯度高,并且经过蛋白酶消化后会产生特征明确的产物,因此对CRP与组蛋白的结合进行了研究。组蛋白H1用凝血酶和胰蛋白酶消化产生三个不同的片段,即N端、中央球状和C端片段。结果表明CRP仅与C端片段结合。还研究了CRP与组蛋白H2A的结合。C端片段的切割并未减少CRP的结合,但当测试H2A的中央球状区域时,CRP的结合大大减少。制备了与H2A的N端和C端片段相同的肽。H2A的N端(15个氨基酸)片段可阻断CRP诱导的磷酸胆碱偶联牛血清白蛋白和组蛋白H2A的沉淀,而C端片段则无抑制作用。因此,我们确定了首个报道的蛋白质上的CRP结合决定因素。