Amine boranes as alternative reducing agents for reductive alkylation of proteins

The use of several commercially available amine-borane complexes was investigated for the reductive methylation of amino groups of several proteins. An earlier study in our laboratory, using turkey ovomucoid as the model protein, showed that dimethylamine borane is a slightly weaker reducing agent,...

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Published inAnalytical biochemistry Vol. 124; no. 2; pp. 272 - 278
Main Authors Cabacungan, Judy C., Ahmed, Ahmed I., Feeney, Robert E.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.08.1982
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Abstract The use of several commercially available amine-borane complexes was investigated for the reductive methylation of amino groups of several proteins. An earlier study in our laboratory, using turkey ovomucoid as the model protein, showed that dimethylamine borane is a slightly weaker reducing agent, but a good, less toxic substitute for sodium cyanoborohydride ( K. F. Geoghegan, J. C. Cabacungan, H. B. F. Dixon, and R. E. Feeney, 1981, Int. J. Peptide Protein Res. 17, 345–352). N-α-Acetyl- l-lysine, poly- l-lysine, turkey ovomucoid, bovine serum albumin, chicken ovalbumin, β-lactoglobulin, casein, and soybean protein were reductively methylated with dimethylamine borane and trimethylamine borane. The latter produced a consistently lower degree of modification even in the presence of sodium dodecyl sulfate. In a comparison that included the boranes triethylamine, t-butylamine, morpholine, and pyridine, pyridine borane was found to be slightly stronger than sodium cyanoborohydride. In a pH 7 solution containing 2 m m N-α-acetyl- l-lysine and 20 m m formaldehyde, complete dimethylation was achieved with about 10 m m pyridine borane after 2 h incubation at 22°C, while more than 15 m m was necessary with sodium cyanoborohydride. Like dimethylamine borane, both pyridine borane and triethylamine borane showed a reducing capacity at pH 7 which was as high as that at pH 9. Reductive alkylation under neutral to mild acid conditions allows modification of alkaline labile proteins and also limits the side reactions between proteins and formaldehyde.
AbstractList The use of several commercially available amine-borane complexes was investigated for the reductive methylation of amino groups of several proteins. An earlier study in our laboratory, using turkey ovomucoid as the model protein, showed that dimethylamine borane is a slightly weaker reducing agent, but a good, less toxic substitute for sodium cyanoborohydride ( K. F. Geoghegan, J. C. Cabacungan, H. B. F. Dixon, and R. E. Feeney, 1981, Int. J. Peptide Protein Res. 17, 345–352). N-α-Acetyl- l-lysine, poly- l-lysine, turkey ovomucoid, bovine serum albumin, chicken ovalbumin, β-lactoglobulin, casein, and soybean protein were reductively methylated with dimethylamine borane and trimethylamine borane. The latter produced a consistently lower degree of modification even in the presence of sodium dodecyl sulfate. In a comparison that included the boranes triethylamine, t-butylamine, morpholine, and pyridine, pyridine borane was found to be slightly stronger than sodium cyanoborohydride. In a pH 7 solution containing 2 m m N-α-acetyl- l-lysine and 20 m m formaldehyde, complete dimethylation was achieved with about 10 m m pyridine borane after 2 h incubation at 22°C, while more than 15 m m was necessary with sodium cyanoborohydride. Like dimethylamine borane, both pyridine borane and triethylamine borane showed a reducing capacity at pH 7 which was as high as that at pH 9. Reductive alkylation under neutral to mild acid conditions allows modification of alkaline labile proteins and also limits the side reactions between proteins and formaldehyde.
Author Cabacungan, Judy C.
Ahmed, Ahmed I.
Feeney, Robert E.
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Snippet The use of several commercially available amine-borane complexes was investigated for the reductive methylation of amino groups of several proteins. An earlier...
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SubjectTerms Alkylation
Amines
Boranes
Indicators and Reagents
Methylation
Oxidation-Reduction
Proteins - analysis
Structure-Activity Relationship
Title Amine boranes as alternative reducing agents for reductive alkylation of proteins
URI https://dx.doi.org/10.1016/0003-2697(82)90038-0
https://www.ncbi.nlm.nih.gov/pubmed/7149226
https://search.proquest.com/docview/80207014
Volume 124
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