Identification of Protease Specificity Using Biotin-Labeled Substrates

  • Yamamoto H
  • Saito S
  • Sawaguchi Y
  • et al.
1Citations
Citations of this article
13Readers
Mendeley users who have this article in their library.

Abstract

© 2017 Yamamoto et al. Background: Proteolysis constitutes a major post-translational modification. For example, proteases regulate the activation or inactivation of various proteins, such as enzymes, growth factors, and peptide hormones. Proteases have substrate specificity, and protease expression regulates the specific and regional activation or inactivation of several functional proteins. Methods: We demonstrate a novel method for determining protease specificity through the use of MALDI-TOF mass spectrometry with biotinlabeled substrates. Results: This method was able to determine the specificity of TPCK-trypsin, V8 protease, elastase and cyanogen bromide cleavage, and the results were similar to previous reports. In addition, the method can be used to measure crude samples, such as tumor extracts. Conclusion: We demonstrated that this method could identify protease specificity after simple processing, even for crude samples.

Cite

CITATION STYLE

APA

Yamamoto, H., Saito, S., Sawaguchi, Y., & Kimura, M. (2017). Identification of Protease Specificity Using Biotin-Labeled Substrates. The Open Biochemistry Journal, 11(1), 27–35. https://doi.org/10.2174/1874091x01711010027

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free