Frink R J, Eisenberg D, Glitz D G
Proc Natl Acad Sci U S A. 1978 Dec;75(12):5778-82. doi: 10.1073/pnas.75.12.5778.
Antibodies to the nucleosidel,N(6)-ethenoadenosine have been used to localize the site of adenylylation of the glutamine synthetase [L-glutamate:ammonia ligase (ADP-forming), EC 6.3.1.2] of Escherichia coli. Antibodies were induced in rabbits by injection of a bovine albumin-ethenoadenosine conjugate. The resulting antisera strongly bound ethenoadenosine, its 5'-nucleotide, or protein conjugates of the nucleoside; little or no crossreaction was seen to adenosine, AMP, or the protein carrier. Ethenoadenylylated glutamine synthetase was prepared by modification of the enzyme by the E. coli adenylyltransferase, using etheno-ATP as a substrate. The ethenoadenylylated glutamine synthetase was precipitated by antibodies to ethenoadenosine in conjunction with goat anti-rabbit gamma globulin. Electron micrographs of reaction mixtures of ethenoadenylylated glutamine synthetase and anti-ethenoadenosine showed individual enzyme molecules complexed with one or more antibodies and pairs of enzyme molecules crosslinked by a single antibody. The approximate site of adenylylation was located from the apparent area of contact between enzyme and antibody. We conclude that the adenylylation sites are on the periphery of the bilayered hexagonal disc, offset by 15 +/- 10 degrees from the 2-fold axis of symmetry through a vertex of the hexagon and 20 +/- 10 A from the plane between the layers of the disc.
针对核苷N(6)-乙烯腺苷的抗体已被用于定位大肠杆菌谷氨酰胺合成酶[L-谷氨酸:氨连接酶(ADP形成),EC 6.3.1.2]腺苷酸化的位点。通过注射牛血清白蛋白-乙烯腺苷偶联物在兔体内诱导产生抗体。所得抗血清能强烈结合乙烯腺苷、其5'-核苷酸或该核苷的蛋白质偶联物;与腺苷、AMP或蛋白质载体几乎没有交叉反应。通过使用乙烯基ATP作为底物,利用大肠杆菌腺苷酸转移酶对谷氨酰胺合成酶进行修饰来制备乙烯腺苷酸化的谷氨酰胺合成酶。乙烯腺苷酸化的谷氨酰胺合成酶与抗乙烯腺苷的抗体以及山羊抗兔γ球蛋白结合后沉淀。乙烯腺苷酸化的谷氨酰胺合成酶与抗乙烯腺苷反应混合物的电子显微镜照片显示,单个酶分子与一种或多种抗体形成复合物,成对的酶分子由单个抗体交联。腺苷酸化的大致位点是根据酶与抗体之间明显的接触区域确定的。我们得出结论:腺苷酸化位点位于双层六边形盘的周边,相对于通过六边形一个顶点的二次对称轴偏移15±1 °,并且距离盘层之间的平面20±10 Å。