1990Journal of the Chemical Society Chemical CommunicationsRequires access

A sensitive method for the determination of the primary amide function (RCONH2) in peptides by mass spectrometry

Jennifer C. Nutkins, Dudley H. Williams

Open publisher page 3 citations

Abstract

Several model peptides have been trimethylsilylated and their FIB mass spectra obtained; reaction was detected at hydroxy groups and primary amides only, amines and carboxy groups were observed in underivatised form, and thus, in conjunction with standard procedures for the determination of hydroxy groups, this methodology represents a sensitive and extremely rapid means for the detection of primary amides in such molecules.

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What this paper is about

Several model peptides have been trimethylsilylated and their FIB mass spectra obtained; reaction was detected at hydroxy groups and primary amides only, amines and carboxy groups were observed in underivatised form, and thus, in conjunction with standard procedures for the determination of hydroxy groups, this methodology represents a sensitive and extremely rapid means for the detection of primary amides in such molecules.

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Available abstract

Several model peptides have been trimethylsilylated and their FIB mass spectra obtained; reaction was detected at hydroxy groups and primary amides only, amines and carboxy groups were observed in underivatised form, and thus, in conjunction with standard procedures for the determination of hydroxy groups, this methodology represents a sensitive and extremely rapid means for the detection of primary amides in such molecules.

Key concepts: Primary (astronomy), Chemistry, Amide, Mass spectrometry, Protein primary structure, Function (biology), Peptide, Chromatography

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