Chuan H, Wang J H
Bioenergetics Laboratory, State University, Buffalo, New York 14214-3094.
J Biol Chem. 1988 Sep 15;263(26):13003-6.
The affinity reagents 3'-O-(5-fluoro-2,4-dinitrophenyl)ADP ether (FDNP-ADP) and 3'-O-(5-fluoro-2,4-dinitrophenyl)ATP ether (FDNP-ATP) were synthesized and characterized. FDNP[14C]ADP was found to label the active site of mitochondrial F1-ATPase slowly at room temperature but with high specificity. F1 was effectively protected from the labeling reagent by ATP or ADP. An average number of 1.3 covalent label per F1 is sufficient for 100% inhibition of the ATPase. About 73% of the radioactive label was found covalently attached to beta subunits, 9% on alpha, practically none on gamma, delta, and epsilon. Cleavage of the labeled enzyme by pepsin and sequencing of the major radioactive peptide showed that the labeled amino acid residue in beta subunit was Lys beta 162. These results show that Lys beta 162 is indeed at the active site of F1 as assumed in the recently proposed models (Fry, D. C., Kuby, S. A., and Mildvan, A. S. (1986) Proc. Natl. Acad. Sci. U. S. A. 83, 907-911; Duncan, I. M., Parsonage, D., and Senior, A. E. (1986) FEBS Lett. 208, 1-6).
合成并表征了亲和试剂3'-O-(5-氟-2,4-二硝基苯基)ADP醚(FDNP-ADP)和3'-O-(5-氟-2,4-二硝基苯基)ATP醚(FDNP-ATP)。发现FDNP[14C]ADP在室温下能缓慢标记线粒体F1-ATP酶的活性位点,但具有高特异性。ATP或ADP能有效保护F1免受标记试剂的作用。每个F1平均有1.3个共价标记足以100%抑制ATP酶。发现约73%的放射性标记共价连接在β亚基上,9%在α亚基上,γ、δ和ε亚基上几乎没有。用胃蛋白酶裂解标记的酶并对主要放射性肽进行测序表明,β亚基中的标记氨基酸残基是Lysβ162。这些结果表明,Lysβ162确实如最近提出的模型(Fry, D. C., Kuby, S. A., and Mildvan, A. S. (1986) Proc. Natl. Acad. Sci. U. S. A. 83, 907-911; Duncan, I. M., Parsonage, D., and Senior, A. E. (1986) FEBS Lett. 208, 1-6)所假设的那样位于F1的活性位点。