Good buffer

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A good buffer ( English Good's buffer ) is a buffer used in biochemistry according to the criteria of Norman Good .

properties

Between 1966 and 1980, Norman E. Good and co-workers developed twenty substances for use as buffers. In contrast to other buffer substances, Good buffers should have as few interactions with proteins as possible , high solubility , no diffusion through biomembrane , a buffer range between pH 6 and 8, low toxicity , low UV absorption , independence of the buffer effect from other factors, be inexpensive to manufacture and have metabolic and chemical stability. Some Good buffers are zwitterions , e.g. B. Morpholinoethanesulfonic acid (MES), 3- (N-Morpholino) propanesulfonic acid (MOPS), ADA, BES and Bicine.

Representative

The following table contains the effective pK a values measured by Good at 20 ° C. and at a concentration of about 100 mM. The resulting pH values ​​depend on the concentration and temperature.

buffer pK a at 20 ° C ΔpK a / ° C Solubility in water at 0 ° C
MES 6.15 −0.011 0.65M
ADA 6.62 −0.011 -
PIPES 6.82 −0.0085 -
ACES 6.88 −0.020 0.22M
MOPSO 6.95 −0.015 0.75M
Cholamine chloride 7.10 −0.027 4.2M (as HCl)
PUG 7.15 −0.013 high
BES 7.17 −0.016 3.2M
TES 7.5 −0.020 2.6M
HEPES 7.55 −0.014 2.25M
DIPSO 7.6 −0.015 0.24M
Acetamidoglycine 7.7 - very high
TAPSO 7.7 −0.018 1.0M
POPSO 7.85 −0.013 -
HEPPSO 7.9 −0.01 2.2M
HEPPS 8.1 −0.015 high
Tricine 8.15 −0.021 0.8M
Glycinamide 8.2 −0.029 6.4M (as HCl)
Bicine 8.35 −0.018 1.1M
TAPS 8.55 −0.027 high

Three of the Good buffers have little tendency to complex metal ions, MES, MOPS and PIPES. Piperazine -containing buffers (PIPES, HEPES, POPSO and HEPPS) can form radicals and should therefore be avoided in redox studies . Tricine is flavines photo-oxidized and reduces under sunlight the activity of flavones -containing enzymes . The acids of ADA, POPSO and PIPES are sparingly soluble. ADA absorbs UV light below a wavelength of 260 nm, ACES absorbs below 230 nm.

After Good, several other Good buffers were developed, e.g. B. AMPSO , CABS , CHES , CAPS , CAPSO .

Individual evidence

  1. ^ Norman E. Good, G. Douglas Winget, Wilhelmina Winter, Thomas N. Connolly, Seikichi Izawa, Raizada MM Singh: Hydrogen Ion Buffers for Biological Research . In: Biochemistry . 5, No. 2, 1966, pp. 467-477. doi : 10.1021 / bi00866a011 . PMID 5942950 .
  2. ^ Norman E. Good, Seikichi Izawa: Hydrogen ion buffers . In: Methods Enzymol. . 24, 1972, pp. 53-68. doi : 10.1016 / 0076-6879 (72) 24054-x . PMID 4206745 .
  3. ^ WJ Ferguson, KI Braunschweiger, WR Braunschweiger, JR Smith, JJ McCormick, CC Wasmann, NP Jarvis, DH Bell et al .: Hydrogen Ion Buffers for Biological Research . In: Anal Biochem . 104, No. 2, 1980, pp. 300-310. doi : 10.1016 / 0003-2697 (80) 90079-2 . PMID 7446957 .
  4. ^ R. Goldberg, Kishore, N .; Lennen, R .: Thermodynamic Quantities for the Ionization Reactions of Buffers . In: J. Phys. Chem. Ref. Data . 31, No. 2, 2002, pp. 231-370. doi : 10.1063 / 1.1416902 .
  5. JK Grady, ND Chasteen, DC Harris: Radicals from "Good's" buffers . In: Anal. Biochem. . 173, No. 1, 1988, pp. 111-115. doi : 10.1016 / 0003-2697 (88) 90167-4 . PMID 2847586 .
  6. M. Kirsch, EE Lomonosova, H.-G. Korth, R. Sustmann, H. de Groot: Hydrogen peroxide formation by reaction of peroxynitrite with HEPES and related tertiary amines. Implications for a general mechanism . In: J Biol Chem . 273, No. 21, 1998, pp. 12716-12724. doi : 10.1074 / jbc.273.21.12716 . PMID 9582295 .