Scinovex
article Open AccessTop 1% cited

Protein thiolation and reversible protein-protein conjugation. <i>N</i>-Succinimidyl 3-(2-pyridyldithio)propionate, a new heterobifunctional reagent

Biochemical Journal · 1978 · Vol. 173(3) · pp. 723–737
J. CarlssonHåkan DrevinRolf Axén

Abstract

A heterobifunctional reagent, N-succinimidyl 3-(2-pyridyldithio)propionate, was synthesized. Its N-hydroxysuccinimide ester group reacts with amino groups and the 2-pyridyl disulphide structure reacts with aliphatic thiols. A new thiolation procedure for proteins is based on this reagent. The procedure involves two steps. First, 2-pyridyl disulphide structures are introduced into the protein by the reaction of some of its amino groups with the N-hydroxysuccinimide ester sie of the reagent. The protein-bound 2-pyridyl disulphide structures are then reduced with dithiothreitol. This reaction can be carried out without concomitant reduction of native disulphide bonds. The technique has been used for the introduction of thiol groups de novo into ribonuclease, gamma-globulin, alpha-amylase and horseradish peroxidase. N-Succinimidyl 3-(2-pyridyldithio)propionate can also be used for the preparation of protein-protein conjugates. This application is based on the fact that protein-2-pyridyl disulphide derivatives (formed from the reaction of non-thiol proteins with the reagent) react with thiol-containing proteins (with native thiols or thiolated by, for example, the method described above) via thiol-disulphide exchange to form disulphide-linked protein-protein conjugates. This conjugation technique has been used for the preparation of an alpha-amylase-urease, a ribonuclease-albumin and a peroxidase-rabbit anti-(human transferrin) antibody conjugate. The disulphide bridges between the protein molecules can easily be split by reduction or by thiol-disulphide exchange. Thus conjugation is reversible. This has been demonstrated by scission of the ribonuclease-albumin and the alpha-amylase-urease conjugate into their components with dithiothreitol. N-Succinimidyl 3-(2-pyridyldithio)propionate has been prepared in crystalline form, in which state (if protected against humidity) it is stable on storage at room temperature (23 degrees C).

Enzyme Production and CharacterizationPeptidase Inhibition and AnalysisProtein purification and stabilityChemistryPropionateThiolReagentConjugateDithiothreitolAlbuminHorseradish peroxidaseRibonucleaseBiochemistry

MeSH terms

ChemistryChromatography, GelEnzymesIndicators and ReagentsProtein BindingProteinsPyridinesSuccinimidesSulfhydryl CompoundsChemical Phenomena
Citations
1,219
FWCI
14.52
field-weighted impact
References
24
Percentile
99%
vs. same field & year
Citations per year
References
Determination of sulfhydryl groups with 2,2′- or 4,4′-dithiodipyridine
Archives of Biochemistry and Biophysics · 1967 · 991 citations
Citation Network

How this paper connects to the literature. Drag to explore, click any node to open that paper.

Protein thiolation and reversible protein-protein conjugation. <i>N</i>-Succinimidyl 3-(2-pyridyldithio)propionate, a new heterobifunctional reagent · Scinovex