Chemical proteomic analysis of 6-benzylaminopurine molecular partners in wheat grains
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články
Grantová podpora
LO1204
Ministry of Education, Youth and Sports, Czech Republic
PubMed
28688084
DOI
10.1007/s00299-017-2174-4
PII: 10.1007/s00299-017-2174-4
Knihovny.cz E-zdroje
- Klíčová slova
- Affinity purification, Chemical proteomics, Cytokinin, Molecular target identification, Plant proteomics, Wheat,
- MeSH
- benzylové sloučeniny metabolismus MeSH
- chromatografie kapalinová MeSH
- cytokininy metabolismus MeSH
- elektroforéza v polyakrylamidovém gelu MeSH
- jedlá semena metabolismus MeSH
- proteom metabolismus MeSH
- proteomika metody MeSH
- pšenice metabolismus MeSH
- puriny metabolismus MeSH
- rostlinné proteiny metabolismus MeSH
- tandemová hmotnostní spektrometrie MeSH
- vazba proteinů MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- benzylaminopurine MeSH Prohlížeč
- benzylové sloučeniny MeSH
- cytokininy MeSH
- proteom MeSH
- puriny MeSH
- rostlinné proteiny MeSH
An affinity-based chemical proteomic technique enabled direct identification of BAP-interacting proteins in wheat, including the well-known cytokinin-binder, cytokinin-binding protein 1. In this work, we show the development of a chemical proteomic technique for the identification of proteins binding to natural aromatic cytokinins (CKs). 6-benzylaminopurine (BAP) and documented CK-binder, wheat germ-allocated cytokinin-binding protein 1 (CBP-1), were suggested as an ideal proof-of concept affinity pair. Therefore, wheat grains were chosen as a model plant material. The BAP affinity beads were prepared by the immobilization of synthesized BAP-derived ligand to a commercial, pre-activated resin and used to isolate target proteins. The proteomic analysis of complex plant extracts is often complicated by the presence of highly abundant background proteins; in this case, the omnipresent alpha-amylase inhibitors (AAIs). To cope with this problem, we included SDS-PAGE, in-gel trypsin digestion and fraction pooling prior to shotgun analysis, which brought about an obvious drop in the signals belonging to the obstructing proteins. This was accompanied by a sharp increase in the number of identified BAP targets in comparison to a conventional in-solution digestion approach. To distinguish specific CK-binding proteins from those having a general affinity for nucleotide-like compounds, competitive pull-downs with natural nucleotides and free BAP were included in every affinity experiment. By this approach, we were able to identify a group of BAP-interacting proteins, which were subsequently found to be related to biological processes affected by CKs. Moreover, the selected affinity enrichment strategy was verified by the detection of the aforementioned CK-interacting protein, CBP-1. We propose that the developed method represents a promising tool for appealing research of as yet unknown CK molecular partners in plants.
Zobrazit více v PubMed
Nat Chem Biol. 2010 Apr;6(4):291-9 PubMed
Eur J Biochem. 2002 Jan;269(2):397-412 PubMed
BMC Genomics. 2006 Sep 08;7:229 PubMed
Nature. 1970 Aug 15;227(5259):680-5 PubMed
J Proteome Res. 2006 Jun;5(6):1435-47 PubMed
Nat Biotechnol. 2011 Mar;29(3):255-65 PubMed
Dev Cell. 2011 Oct 18;21(4):796-804 PubMed
Nat Protoc. 2006;1(6):2856-60 PubMed
Nat Protoc. 2007;2(8):1896-906 PubMed
Plant J. 2016 Jan;85(1):134-47 PubMed
Science. 1995 Dec 22;270(5244):1986-8 PubMed
Nucleic Acids Res. 2007 Jan;35(Database issue):D846-51 PubMed
J Proteome Res. 2010 Nov 5;9(11):6033-43 PubMed
Physiol Plant. 2010 Mar;138(3):249-55 PubMed
Front Plant Sci. 2012 Jan 31;3:8 PubMed
Electrophoresis. 2004 May;25(9):1327-33 PubMed
Biochim Biophys Acta. 2016 Aug;1864(8):1003-15 PubMed
Physiol Plant. 2003 Apr;117(4):453-458 PubMed
J Exp Bot. 2015 Aug;66(16):4863-71 PubMed
Plant J. 2006 Mar;45(6):1028-36 PubMed
ChemMedChem. 2010 Nov 8;5(11):1927-36 PubMed
J Proteome Res. 2006 Sep;5(9):2283-93 PubMed
Curr Opin Biotechnol. 2003 Feb;14(1):87-95 PubMed
Mol Cell Proteomics. 2005 Dec;4(12):2010-21 PubMed
Curr Opin Plant Biol. 2009 Oct;12(5):527-38 PubMed
Plant Cell Environ. 2009 Sep;32(9):1147-60 PubMed
Plant Physiol. 1985 Nov;79(3):706-10 PubMed
Front Plant Sci. 2013 Nov 19;4:451 PubMed
J Exp Bot. 2008;59(10):2659-72 PubMed
Mol Biosyst. 2009 May;5(5):472-82 PubMed
J Exp Bot. 2011 Jan;62(3):921-37 PubMed
J Proteome Res. 2009 Oct;8(10):4753-65 PubMed
Nat Chem Biol. 2009 Sep;5(9):616-24 PubMed
Proteome Sci. 2011 Feb 11;9:10 PubMed
J Proteome Res. 2013 Sep 6;12(9):4005-17 PubMed
J Exp Bot. 2012 Apr;63(7):2825-32 PubMed
Plant Physiol. 1981 Jan;67(1):156-62 PubMed
Unique organization of photosystem II supercomplexes and megacomplexes in Norway spruce