A simplified procedure to determine tryptophan residues in proteins. |
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Authors: | Y D Karkhanis D J Carlo J Zeltner |
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Affiliation: | The Merck Institute for Therapeutic Research, Rahway, New Jersey 07065 USA |
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Abstract: | A procedure is described to determine tryptophan residues in proteins using a tryptophan reagent, 2-hydroxy-5-nitrobenzyl bromide. The method involves the treatment of the unfolded protein with the reagent in 9 m urea at acid pH; incubation of the mixture at room temperature for 2 hr and the removal of the excess reagent by centrifugation and gel filtration. The amount of tryptophan in a protein is determined from the optical density of the labeled protein at 280 and 410 nm, and from the known optical density of 1 mg/ml of the protein at 280 nm and of the reagent at 280 and 410 nm. The efficacy of the method was tested with eight proteins whose tryptophan content is known. |
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Keywords: | To whom inquiries about the paper should be addressed. |
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