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. Author manuscript; available in PMC: 2014 Dec 4.
Published in final edited form as: Proteomics. 2012 May;12(10):1527–1546. doi: 10.1002/pmic.201100599

Table 1. List of high-throughput methods for characterizing binding specificity, their advantages and disadvantages.

Method Peptide Library Size Quantitative Advantages Disadvantage
Peptide Array 10-1000’s Semi-Quantitative
  • Study PTMs

  • Generate negative binding data

  • Easy to generate different libraries

  • Biased libraries (a priori knowledge)

  • High cost of materials

Protein Microarrays 10-100’s Quantitative
  • Quantitative

  • Protein stability

  • Limitation in number of peptides

Phage Display 1×10ˆ10 Not quantitative
  • random peptides

  • large quantities of the library

  • low costs for production

  • Only natural amino acids, no PTMs

  • high cost in DNA sequencing

Mass Spectrometry 10-100’s Not quantitative
  • Physiological

  • Transient interactions are lost

  • Limited to specific tissues or cells