%0 Journal Article %1 hanke2011cyclic %A Hanke, S. E. %A Bertinetti, D. %A Badel, A. %A Schweinsberg, S. %A Genieser, H. G. %A Herberg, F. W. %D 2011 %J N Biotechnol %K herberg myown %N 4 %P 294-301 %R 10.1016/j.nbt.2010.12.001 %T Cyclic nucleotides as affinity tools: phosphorothioate cAMP analogues address specific PKA subproteomes %U http://www.ncbi.nlm.nih.gov/pubmed/21147280?dopt=Abstract %V 28 %X cAMP (adenosine-3',5'-cyclic monophosphate) is a general second messenger controlling distinct targets in eukaryotic cells. In a (sub)proteomic approach, two classes of phosphorothioate cAMP affinity tools were used to isolate and to identify signalling complexes of the main cAMP target, cAMP dependent protein kinase (PKA). Agonist analogues (here: Sp-cAMPS) bind to the regulatory subunits of PKA (PKA-R), together with their interaction partners, and cause dissociation of a holoenzyme complex comprising PKA-R and catalytic subunits of PKA (PKA-C). Antagonist analogues (here: Rp-cAMPS) bind to the holoenzyme without dissociating the complex and were developed to identify interaction partners that bind to the entire complex or to PKA-C. More than 80 different proteins were isolated from tissue extracts including several PKA isoforms and known as well as potentially new interaction partners. Nevertheless, unspecific binding of general nucleotide binding proteins limited the outcome of this chemical proteomics approach. Surface plasmon resonance (SPR) was employed to optimise the entire workflow of pull down proteomics and to quantify the effects of different nucleotides (ATP, ADP, GTP and NADH) on PKA-R binding to affinity material. We could demonstrate that the addition of NADH to lysates improved specificity in pull down experiments. Using a combination of SPR studies and pull down experiments it was shown unambiguously that it is possible to specifically elute protein complexes with cAMP or cGMP from cAMPS analogue matrices. The side-by-side analysis of the PKA-R interactome and the holoenzyme complexed with interacting proteins will contribute to a further dissection of the multifaceted PKA signalling network.

@article{hanke2011cyclic, abstract = {cAMP (adenosine-3',5'-cyclic monophosphate) is a general second messenger controlling distinct targets in eukaryotic cells. In a (sub)proteomic approach, two classes of phosphorothioate cAMP affinity tools were used to isolate and to identify signalling complexes of the main cAMP target, cAMP dependent protein kinase (PKA). Agonist analogues (here: Sp-cAMPS) bind to the regulatory subunits of PKA (PKA-R), together with their interaction partners, and cause dissociation of a holoenzyme complex comprising PKA-R and catalytic subunits of PKA (PKA-C). Antagonist analogues (here: Rp-cAMPS) bind to the holoenzyme without dissociating the complex and were developed to identify interaction partners that bind to the entire complex or to PKA-C. More than 80 different proteins were isolated from tissue extracts including several PKA isoforms and known as well as potentially new interaction partners. Nevertheless, unspecific binding of general nucleotide binding proteins limited the outcome of this chemical proteomics approach. Surface plasmon resonance (SPR) was employed to optimise the entire workflow of pull down proteomics and to quantify the effects of different nucleotides (ATP, ADP, GTP and NADH) on PKA-R binding to affinity material. We could demonstrate that the addition of NADH to lysates improved specificity in pull down experiments. Using a combination of SPR studies and pull down experiments it was shown unambiguously that it is possible to specifically elute protein complexes with cAMP or cGMP from cAMPS analogue matrices. The side-by-side analysis of the PKA-R interactome and the holoenzyme complexed with interacting proteins will contribute to a further dissection of the multifaceted PKA signalling network.}, added-at = {2011-10-24T13:52:24.000+0200}, author = {Hanke, S. E. and Bertinetti, D. and Badel, A. and Schweinsberg, S. and Genieser, H. G. and Herberg, F. W.}, biburl = {https://www.bibsonomy.org/bibtex/2d29a7a4f0e4294623ca111fa758b8963/biochemie}, doi = {10.1016/j.nbt.2010.12.001}, interhash = {c70c37b4c6b2b07979c173c17136d948}, intrahash = {d29a7a4f0e4294623ca111fa758b8963}, journal = {N Biotechnol}, keywords = {herberg myown}, month = jul, number = 4, pages = {294-301}, pmid = {21147280}, timestamp = {2012-07-24T09:38:37.000+0200}, title = {Cyclic nucleotides as affinity tools: phosphorothioate cAMP analogues address specific PKA subproteomes}, url = {http://www.ncbi.nlm.nih.gov/pubmed/21147280?dopt=Abstract}, volume = 28, year = 2011 }