A new functional, chemical proteomics technology to identify purine nucleotide binding sites in complex proteomes.

Adenine nucleotides are small, abundant molecules that bind numerous proteins involved in pivotal cellular processes. These nucleotides are co-factors or substrates for enzymes, regulators of protein function, or structural binding motifs. The identification of nucleotide-binding sites on a proteome-wide scale is tempting in view of the high number of nucleotide-binding proteins, their large in vivo concentration differences, and the various functions they exert. Here, we report on a functional, chemical, gel-free proteomics technology that allows the identification of protein adenine nucleotide-binding site(s) in cell lysates. Our technology uses a synthetic ATP analogue, 5'-p-fluorosulfonylbenzoyladenosine (FSBA), as an affinity/activity-based probe for nucleotide-binding sites. When applied on a cellular level, 185 different FSBA-labeled sites in a human Jurkat cell lysate were identified. Functional and structural aspects of the use of FSBA on a proteome-wide scale are discussed.

Citation

Xavier Hanoulle, Jozef Van Damme, An Staes, Lennart Martens, Marc Goethals, Joël Vandekerckhove, Kris Gevaert. A new functional, chemical proteomics technology to identify purine nucleotide binding sites in complex proteomes. Journal of proteome research. 2006 Dec;5(12):3438-45

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PMID: 17137346

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