Short, strong hydrogen bonds on enzymes: NMR and mechanistic studies

被引:58
|
作者
Mildvan, AS
Massiah, MA
Harris, TK
Marks, GT
Harrison, DHT
Viragh, C
Reddy, PM
Kovach, IM
机构
[1] Johns Hopkins Univ, Sch Med, Dept Biol Chem, Baltimore, MD 21205 USA
[2] Med Coll Wisconsin, Dept Biochem, Milwaukee, WI 53226 USA
[3] Catholic Univ Amer, Dept Chem, Washington, DC 20064 USA
关键词
short; strong hydrogen bonds; phosphoglycolohydroxamic acid; nucleic acids;
D O I
10.1016/S0022-2860(02)00212-0
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The lengths of short, strong hydrogen bonds (SSHBs) on enzymes have been determined with high precision (+/-0.05 A) from the chemical shifts (delta), and independently from the D/H fractionation factors (phi) of the highly deshielded protons involved. These H-bond lengths agree well with each other and with those found by protein X-ray crystallography, within the larger errors' of the latter method (+/-0.2 to +/-0.8 Angstrom) [Proteins 35 (1999) 275]. A model dihydroxy-naphthalene compound shows a SSHB of 2.54 +/- 0.04 Angstrom based on delta = 17.7 ppm and phi = 0.56 0.04, in agreement with the high resolution X-ray distance of 2.55 +/- 0.06 Angstrom. On ketosteroid isomerase, a SSHB is found (2.50 +/- 0.02 Angstrom), based on delta = 18.2 ppm. and phi = 0.34, from Tyr-14 to the 3-O- of estradiol, an analog of the enolate intermediate. Its strength is similar to7 kcal/mol. On triosephosphate isomerase, SSHBs are found from Glu-165 to the 1-NOH of phosphoglycolohydroxamic acid (PGH), an analog of the enolic intermediate (2.55 +/- 0.05 Angstrom), and from His-95 to the enolic-O- of PGH (2.62 +/- 0.02 Angstrom). In the methylglyoxal synthase-PGH complex, a SSHB (2.51 +/- 0.02 Angstrom) forms between Asp-71 and the NOH of PGH with a strength of greater than or equal to4.7 kcal/mol. When serine proteases bind mechanism-based inhibitors which form tetrahedral Ser-adducts analogous to the tetrahedral intermediates in catalysis, the Asp...His H-bond of the catalytic triad becomes a SSHB [Proc. Natl Acad. Sci. USA 95 (1998) 14664], 2.49-2.63 Angstrom in length. Similarly, on the serine-esterase, butyrylcholinegterase complexed with the mechanism-based inhibitor. m-(N,N,N,-trimethylammonio)-2,2,2-trifluoroacetophenone, a SSHB. forms between Glu-327 and His-438 of the catalytic. triad, 2.61 +/- 0.04 Angstrom in length, based on delta = 18.1 ppm and sigma = 0.65 +/- 0.10. Very similar results are obtained with (human) acetylcholinesterase. The strength of this SSHB is at least 4.9 kcal/mol. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:163 / 175
页数:13
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