Fluorous-based peptide microarrays for protease screening

As ever more protease sequences are uncovered through genome sequencing projects, efficient parallel methods to discover the potential substrates of these proteases becomes crucial. Herein we describe the first use of fluorous-based microarrays to probe peptide sequences and begin to define the scope and limitations of fluorous microarray technologies for the screening of proteases. Comparison of a series of serine proteases showed that their ability to cleave peptide substrates in solution was maintained upon immobilization of these substrates onto fluorous-coated glass slides. The fluorous surface did not serve to significantly inactivate the enzymes. However, addition of hydrophilic components to the peptide sequences could induce lower rates of substrate cleavage with enzymes such as chymotrypsin with affinities to hydrophobic moieties. This work represents the first step to creating robust protease screening platforms using noncovalent microarray interface that can easily incorporate a range of compounds on the same slide.

The first use of noncovalent fluorous-based microarrays to probe peptide sequences begins to define the scope and limitations of fluorous microarray technologies for the screening of proteases. The fluorous surface did not serve to significantly inactivate the enzymes, but linkers must be properly designed to avoid lower rates of substrate cleavage with enzymes such as chymotrypsin with affinities to hydrophobic moieties.Figure optionsDownload as PowerPoint slide