Bigelow D J, Inesi G
Department of Biological Chemistry, University of Maryland School of Medicine, Baltimore 21201.
Biochemistry. 1991 Feb 26;30(8):2113-25. doi: 10.1021/bi00222a016.
We have used fluorescence spectroscopy to characterize three covalently bound spectroscopic maleimide derivatives with respect to their location within the tertiary structure of the Ca-ATPase of sarcoplasmic reticulum (SR). These derivatives include (1) 2-(4'-maleimidoanilino)naphthalene-6-sulfonic acid, (2) 4-(dimethylamino)azobenzene-4'-maleimide, and (3) fluorescein 5'-maleimide. Biochemical assays demonstrate that modification with any of these three derivatives results in the same functional effects, observed following derivatization of cysteines 344 and 364 by N-ethylmaleimide [Saito-Nakatsuka et al. (1987) J. Biochem. (Tokyo) 101, 365-376]. These residues bracket the ATPase's phosphorylation site (Asp 351) and thus may provide spectroscopic probes of the protein's conformation in this essential region. In agreement with sequencing results, SDS-polyacrylamide gels show that maleimide-modified SR exhibits fluorescence exclusively on the A1 tryptic fragment of the Ca-ATPase. Extensive tryptic digestion followed by centrifugation demonstrates essentially all of the fluorescence was associated with the soluble rather than insoluble (membrane-associated) peptides, confirming the predicted extramembranous location of these residues. Utilizing frequency-domain fluorescence spectroscopy, we were able to recover the transient effects associated with a distribution of donor-acceptor distances. We find from these fluorescence resonance energy transfer measurements that covalently bound maleimide probes are 36 A apart, independent of whether a discrete distance is assumed or a distance distribution model is utilized, in which the conformational variability of the protein is taken into account. While a unimodal distance distribution is adequate to describe the intensity decay associated with maleimide-directed donor-acceptor pairs, a bimodal distribution of distances is necessary to describe the frequency response associated with the energy transfer between maleimide-directed chromophores and other covalently bound probes on the Ca-ATPase, consistent with the large spatial separation observed between maleimides. We recover mean distances of 42 and 77 A between maleimide sites and bound FITC (Lys 515) and mean distances of 28 and 37 A between the maleimide- and the iodoacetamide-directed probes (Cys 670 and 674, whose close proximity approximates a single locus). The measured distances are presented in a model and have permitted us to describe a unique arrangement of these covalently bound probes within both the secondary and tertiary structure of the Ca-ATPase. The resolution inherent in the frequency-domain fluorescence technique to multiple donor-acceptor distances should be generally applicable to a wide range of biological systems in which specific labeling of single unique donor-acceptor sites is not feasible.
我们利用荧光光谱法对三种共价结合的光谱学马来酰亚胺衍生物进行了表征,以确定它们在肌浆网(SR)钙ATP酶三级结构中的位置。这些衍生物包括:(1)2-(4'-马来酰亚胺基苯胺基)萘-6-磺酸,(2)4-(二甲基氨基)偶氮苯-4'-马来酰亚胺,以及(3)荧光素5'-马来酰亚胺。生化分析表明,用这三种衍生物中的任何一种进行修饰都会产生相同的功能效应,这与用N-乙基马来酰亚胺对半胱氨酸344和364进行衍生化后观察到的结果相同[Saito-Nakatsuka等人(1987年),《生物化学杂志》(东京)101,365 - 376]。这些残基围绕着ATP酶的磷酸化位点(天冬氨酸351),因此可能为该蛋白在这个关键区域的构象提供光谱学探针。与测序结果一致,SDS - 聚丙烯酰胺凝胶显示,马来酰亚胺修饰的SR仅在钙ATP酶的A1胰蛋白酶片段上表现出荧光。经过广泛的胰蛋白酶消化后再进行离心,结果表明基本上所有的荧光都与可溶性而非不溶性(膜相关)肽相关,这证实了这些残基在膜外的预测位置。利用频域荧光光谱法,我们能够恢复与供体 - 受体距离分布相关的瞬态效应。我们从这些荧光共振能量转移测量中发现,共价结合的马来酰亚胺探针相距36 Å,无论假设的是离散距离还是使用了考虑蛋白质构象变异性的距离分布模型,结果都是如此。虽然单峰距离分布足以描述与马来酰亚胺定向的供体 - 受体对相关的强度衰减,但需要双峰距离分布来描述与马来酰亚胺定向的发色团和钙ATP酶上其他共价结合探针之间的能量转移相关的频率响应,这与观察到的马来酰亚胺之间的大空间分离一致。我们测得马来酰亚胺位点与结合的异硫氰酸荧光素(赖氨酸515)之间的平均距离为42 Å和77 Å,以及马来酰亚胺与碘乙酰胺定向探针(半胱氨酸670和674,它们的紧密接近近似于一个单一位置)之间的平均距离为28 Å和37 Å。测量的距离在一个模型中呈现,这使我们能够描述这些共价结合探针在钙ATP酶二级和三级结构中的独特排列。频域荧光技术对多个供体 - 受体距离的分辨率应该普遍适用于广泛的生物系统,在这些系统中对单个独特的供体 - 受体位点进行特异性标记是不可行的。