Lagarias J C, Klotz A V, Dallas J L, Glazer A N, Bishop J E, O'Connell J F, Rapoport H
Department of Biochemistry and Biophysics, University of California, Davis 95616.
J Biol Chem. 1988 Sep 15;263(26):12977-85.
Previous spectroscopic studies on the phycocyanobilin-containing peptide beta-2T from Synechococcus sp. 6301 C-phycocyanin and the phycoerythrobilin-containing peptide beta-2TP from Porphyridium cruentum B-phycoerythrin indicated a different single thioether mode of attachment, postulated to be through the D-ring of the tetrapyrrole, in contrast to the A-ring linkage established for the other singly linked bilins in these proteins (Bishop, J.E., Lagarias, J.C., Nagy, J. O., Schoenleber, R.W., Rapoport, H., Klotz, A.V., and Glazer, A.N. (1986) J. Biol. Chem. 261, 6790-6796; Klotz, A.V., Glazer, A.N., Bishop, J.E., Nagy, J.O., and Rapoport, H. (1986) J. Biol. Chem. 261, 6797-6805). The crystal structure of Agmenellum quadruplicatum C-phycocyanin at 2.5-A resolution (Schirmer, T., Bode, W., and Huber, R. (1987) J. Mol. Biol., 196, 677-695) supports an A-ring linkage for all three phycocyanobilins. Consequently we have re-evaluated our proposed structural assignments by further 1H NMR studies. Two-dimensional homonuclear correlated and nuclear Overhauser enhancement spectroscopic data presented here show that all three bilins in Synechococcus 6301 C-phycocyanin are attached solely through the A-ring, complementary to the crystallographic data. The evidence from the NMR data for all bilin peptides examined includes the dipoledipole interactions of the 5-H with the 3-H, 3'-H, and a pyrrole methyl group (7-CH3); the corresponding interactions would not be possible in a D-ring-linked bilin. The 5-H also consistently exhibits allylic J-coupling to the 3-H, supporting A-ring linkage assignment. These data are inconsistent with the alternative D-ring linkage assignment since this would involve J-coupling through five bonds. Examination of the phycoerythrobilin beta-2 position in B-phycoerythrin also reveals an A-ring type of attachment by similar criteria. We conclude that all singly linked bilins are attached through the A-ring.
之前对来自聚球藻属6301的含藻蓝胆素肽β-2T(C-藻蓝蛋白)以及来自紫球藻的含藻红胆素肽β-2TP(B-藻红蛋白)的光谱学研究表明,其硫醚连接方式不同,推测是通过四吡咯的D环连接,这与这些蛋白质中其他单连接胆素所确立的A环连接方式不同(毕晓普,J.E.,拉加里亚斯,J.C.,纳吉,J.O.,舍恩勒伯,R.W.,拉波波特,H.,克洛茨,A.V.,和格拉泽,A.N.(1986年)《生物化学杂志》261,6790 - 6796;克洛茨,A.V.,格拉泽,A.N.,毕晓普,J.E.,纳吉,J.O.,和拉波波特,H.(1986年)《生物化学杂志》261,6797 - 6805)。嗜热栖热放线菌C-藻蓝蛋白在2.5埃分辨率下的晶体结构(席尔默,T.,博德,W.,和胡伯,R.(1987年)《分子生物学杂志》,196,677 - 695)支持所有三种藻蓝胆素均通过A环连接。因此,我们通过进一步的¹H NMR研究重新评估了我们提出的结构归属。此处给出的二维同核相关和核Overhauser增强光谱数据表明,聚球藻6301 C-藻蓝蛋白中的所有三种胆素均仅通过A环连接,这与晶体学数据互补。所有检测的胆素肽的NMR数据证据包括5-H与3-H、3'-H以及一个吡咯甲基(7-CH₃)的偶极-偶极相互作用;在D环连接的胆素中,相应的相互作用是不可能的。5-H还始终表现出与3-H的烯丙基J耦合,支持A环连接归属。这些数据与另一种D环连接归属不一致,因为这将涉及通过五个键的J耦合。对B-藻红蛋白中藻红胆素β-2位置的研究也通过类似标准揭示了A环类型的连接。我们得出结论,所有单连接胆素均通过A环连接。