Thiosulfate ion → Bromide ion

HRID 2260482Notes

Reaction equation

HRID 2260482 reaction equation
[K+].[Br-:2].C1C=CC(C(O)=O)=C(C2C3C=CC(O)=CC=3OC3C=2C=CC(C=3)=O)C=1.CC1C=CC(S(NCl)(=O)=O)=CC=1.S([O-])([O-])(=O)=S.[NH2:45][C@H:46]([C:50]([OH:52])=[O:51])[CH2:47][CH2:48][SH:49]>[OH-].[Na+].O.C([O-])([O-])=O.[Na+].[Na+]>[Br-:2].[NH2:45][C@H:46]([C:50]([OH:52])=[O:51])[CH2:47][CH2:48][SH:49]

Participants

10

Procedure

Hcy was further reacted with the BABA-activated BSA solutions prepared above. 20 mM 1-homocysteine was prepared by dissolving 1.5 mg of 1-homocysteine thiolactone in 0.5 ml 1M NaOH, incubating 10 minutes at 37° C. and finally diluting with 2.0 ml Na phosphate, pH 7.0, and 2.5 ml Na phosphate, pH 6.0 (final pH 7). Both BSA solutions prepared above were diluted to 4.0 ml with H2O and 1.0 ml of the Hcy solution was added to each and incubated overnight. The reactions were concentrated on a Centricon 30 and the reaction efficiency was estimated from the Br- concentration of the retained filtrates. Bromide standards were prepared by adding 2 μl of the appropriate KBr stock solutions to 98 μl of the -BABA-NHS reaction filtrate, producing standards with Br- concentrations of 0.0, 0.2, 0.4, 0.8, and 1.0 mM. 20 μl of the prepared Br- standards or 20 μl of the filtrate from the +BABA-NHS reaction were added to 0.9 ml of 0.1M Na citrate pH 5.5, followed by 20 μl of 0.8 mM fluorescein and 10 μl of 0.1M chloramine T. After 10 minutes, 20 μl of 25 mM thiosulfate in 0.2M Na2CO3 was added to stop the reaction and the absorbance recorded for each sample at 515 nm in a 1 cm cell. The absorbance values of the standards were plotted against the Br- concentrations to produce a standard curve, from which the concentration of Br- contained in the +BABA-NHS reaction was determined. From this value an estimate was obtained of the coupling efficiency of the BABA groups on BSA with Hcy. The +BABA-NHS reaction solution was concentrated 4 times on a Centricon 30, diluted with 1 ml 1×PBS (final conc. ~10 mg/ml) and set aside for subsequent antibody development.

Workup

  1. customprepared above
  2. customBoth BSA solutions prepared
  3. additionwas added to each and
  4. waitincubated overnight
  5. concentrationThe reactions were concentrated on a Centricon 30
  6. customto 98 μl of the -BABA-NHS reaction filtrate
  7. customproducing standards with Br- concentrations of 0.0, 0.2, 0.4, 0.8, and 1.0 mM
  8. waitAfter 10 minutes
  9. customthe reaction
  10. concentrationThe absorbance values of the standards were plotted against the Br- concentrations
  11. customto produce a standard curve

Sources & evidence

ORD record
ord-bf7af0fc13474deebdb887e74628e098
Source dataset
uspto-grants-1995_12
Patent number
US05478729

Reaction notes

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