DICARBOXYLIC-ACIDS LINK PROTON-TRANSFER ACROSS A LIQUID MEMBRANE TO THE SYNTHESIS OF ACYL PHOSPHATES - A MODEL FOR P-TYPE H+-ATPASES

被引:3
作者
COLTON, IJ [1 ]
KAZLAUSKAS, RJ [1 ]
机构
[1] MCGILL UNIV,DEPT CHEM,MONTREAL H3A 2K6,PQ,CANADA
关键词
D O I
10.1021/jo00092a023
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
H+-ATPases are ion pumps that link proton transfer across cell membranes to the synthesis or hydrolysis of ATP. A current research goal is to understand the molecular-level mechanism of this linking. We present a chemical model that mimics some features of H+-ATPases by linking proton transfer across a liquid membrane to the synthesis of acyl phosphates using carboxylic acid anhydride intermediates. Citraconic acid (cis-2-methyl-2-butenedioic acid) accelerated the transfer of protons from a pH 0.3 solution across a chloroform liquid membrane to a pH 10 solution. The mechanism involved spontaneous formation of a small amount of citraconic anhydride (0.6%) in the pH 0.3 layer. This anhydride partitioned into the chloroform layer and diffused to the pH 10 layer, where it hydrolyzed, generating two protons. When the pH 10 layer contained phosphate (1.0 M), some of the citraconic anhydride reacted with phosphate to form citraconyl phosphate, 5.0% yield. In separate experiments, we confirmed that citraconyl phosphate had high phosphoryl donor potential by reacting it with morpholine to form a phosphoramidate (11.5% yield) or with fluoride to form fluorophosphonate (32% yield). To demonstrate the link between an acyl phosphate and a proton gradient in the reverse direction, we used succinyl phosphate, whose hydrolysis occurs in two steps: formation of succinic anhydride, which consumes protons, followed by hydrolysis of succinic anhydride, which releases protons. We generated a pH gradient by carrying out these two steps in separate solutions. Hydrolysis of succinyl phosphate (3.9 mmol) at pH 6.00 started with a increase in pH to 6.16 (0.59 mmol of H+ consumed) caused by the formation of succinic anhydride. We extracted this anhydride with dichloromethane and transferred it to a separate solution at pH 6.05. Hydrolysis of the anhydride released protons (0.36 mmol), decreasing the pH to 5.23. Our model suggests that H+-ATPases could use acyl phosphates and carboxylic acid anhydride intermediates to link proton transfer to ATP synthesis or hydrolysis.
引用
收藏
页码:3626 / 3635
页数:10
相关论文
共 56 条
  • [1] SYNTHETIC PEPTIDES AS MODELS FOR ION CHANNEL PROTEINS
    AKERFELDT, KS
    LEAR, JD
    WASSERMAN, ZR
    CHUNG, LA
    DEGRADO, WF
    [J]. ACCOUNTS OF CHEMICAL RESEARCH, 1993, 26 (04) : 191 - 197
  • [2] ALBERTS B, 1989, MOL BIOL CELL, P300
  • [3] ALBERTY RA, 1969, J BIOL CHEM, V244, P3290
  • [4] THE SYNTHESIS OF ACYL PHOSPHATES IN AQUEOUS SOLUTION
    AVISON, AWD
    [J]. JOURNAL OF THE CHEMICAL SOCIETY, 1955, : 732 - 738
  • [5] BALTSCHEFFSKY M, 1986, METHOD ENZYMOL, V126, P538
  • [6] BOCK G, 1988, CIBA F S, V139
  • [7] BRUICE TC, 1966, BIOORG MECH, V2, P71
  • [8] CARAFOLI E, 1992, J BIOENERG BIOMEMBR, V24, P245
  • [9] BIOMIMETIC ION-TRANSPORT - A FUNCTIONAL-MODEL OF A UNIMOLECULAR ION CHANNEL
    CARMICHAEL, VE
    DUTTON, PJ
    FYLES, TM
    JAMES, TD
    SWAN, JA
    ZOJAJI, M
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1989, 111 (02) : 767 - 769
  • [10] SYNTHESIS OF AN ACYLPHOSPHATE DRIVEN BY A PROTON GRADIENT - A MODEL FOR H+-ATPASE
    COLTON, IJ
    KAZLAUSKAS, RJ
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 1992, 57 (26) : 7005 - 7006