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Sequence‐specific determination of protein and peptide concentrations by absorbance at 205 nm

Protein Science · 2013 · Vol. 22(6) · pp. 851–858
Nicholas J. AnthisG. Marius Clore

Abstract

Quantitative studies in molecular and structural biology generally require accurate and precise determination of protein concentrations, preferably via a method that is both quick and straightforward to perform. The measurement of ultraviolet absorbance at 280 nm has proven especially useful, since the molar absorptivity (extinction coefficient) at 280 nm can be predicted directly from a protein sequence. This method, however, is only applicable to proteins that contain tryptophan or tyrosine residues. Absorbance at 205 nm, among other wavelengths, has been used as an alternative, although generally using absorptivity values that have to be uniquely calibrated for each protein, or otherwise only roughly estimated. Here, we propose and validate a method for predicting the molar absorptivity of a protein or peptide at 205 nm directly from its amino acid sequence, allowing one to accurately determine the concentrations of proteins that do not contain tyrosine or tryptophan residues. This method is simple to implement, requires no calibration, and should be suitable for a wide range of proteins and peptides.

Advanced Proteomics Techniques and ApplicationsMass Spectrometry Techniques and ApplicationsProtein purification and stabilityMolar absorptivityAbsorbanceTryptophanTyrosinePeptideEyespotChemistryChromatographySequence (biology)Bradford protein assay

MeSH terms

Amino Acid SequenceMolecular Sequence DataPeptidesProteinsRecombinant ProteinsSpectrophotometry, Ultraviolet

Funding

  • National Institutes of Health
  • NIH Office of the Director
  • National Institute of Diabetes and Digestive and Kidney Diseases
Citations
442
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5.47
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