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Ellman's reagent

Introduction

File:DTNB reaction.png
Reaction of DTNB with a thiol.

Ellman’s reagent (5, 5′-dithiobis-(2-nitrobenzoic acid) or DTNB) is a chemical used for measuring the amount of thiol groups.[1] The compound reacts with a thiol group to release 2-nitro-5-mercaptobenzoic acid (TNB), which has a strong yellow color in water at neutral and alkaline pH. This reaction is rapid and stochiometric, with the addition of one mole of thiol releasing one mole of TNB. The TNB– is quantified in a spectrophotometer by measuring the absorbance of TNB of visible light at 412 nm, using an extinction coefficient of 14,140 MΒ cmβˆ’1.[2]

Ellman’s reagent can be used for measuring low-molecular mass thiols such as glutathione in both pure solutions and biological samples, such as blood.[3] It can also measure the number of thiol groups on proteins.[4]

References

References

  1. ↑ Ellman GL (1959). “Tissue sulfhydryl groups”. Arch. Biochem. Biophys. 82 (1): 70–7. PMIDΒ 13650640.
  2. ↑ Collier HB (1973). “Letter: A note on the molar absorptivity of reduced Ellman’s reagent, 3-carboxylato-4-nitrothiophenolate”. Anal. Biochem. 56 (1): 310–1. PMIDΒ 4764694.
  3. ↑ Sedlak J, Lindsay RH (1968). “Estimation of total, protein-bound, and nonprotein sulfhydryl groups in tissue with Ellman’s reagent”. Anal. Biochem. 25 (1): 192–205. PMIDΒ 4973948.
  4. ↑ Riener CK, Kada G, Gruber HJ (2002). “Quick measurement of protein sulfhydryls with Ellman’s reagent and with 4,4′-dithiodipyridine”. Analytical and bioanalytical chemistry. 373 (4–5): 266–76. PMIDΒ 12110978.
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