-
Something wrong with this record ?
The unraveling of substrate specificity of histone deacetylase 6 domains using acetylome peptide microarrays and peptide libraries
Z. Kutil, L. Skultetyova, D. Rauh, M. Meleshin, I. Snajdr, Z. Novakova, J. Mikesova, J. Pavlicek, M. Hadzima, P. Baranova, B. Havlinova, P. Majer, M. Schutkowski, C. Barinka,
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
30496698
DOI
10.1096/fj.201801680r
Knihovny.cz E-resources
- MeSH
- HEK293 Cells MeSH
- Histone Deacetylase 6 chemistry metabolism MeSH
- Catalytic Domain * MeSH
- Humans MeSH
- Lysine chemistry metabolism MeSH
- Peptide Fragments chemistry metabolism MeSH
- Static Electricity MeSH
- Substrate Specificity MeSH
- Protein Binding MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Histone deacetylase 6 (HDAC6) is a multidomain cytosolic hydrolase acting mostly on nonhistone protein substrates. Investigations of the substrate specificity of HDAC6 are confounded by the presence of 2 catalytically active deacetylase domains (DD1 and DD2). In this study, acetylome peptide microarrays and peptide libraries were used to map the substrate specificity of DD1 and DD2 of human HDAC6. The results show that DD1 is solely responsible for the deacetylation of substrates harboring the acetyllysine at their C terminus, whereas DD2 exclusively deacetylates peptides with an internal acetyllysine residue. Also, statistical analysis of the deacetylation data revealed amino acid preferences at individual positions flanking the acetyllysine, where glycine and arginine residues are favored at positions N-terminal to the central acetyllysine; negatively charged glutamate is strongly disfavored throughout the sequence. Finally, the deacylation activity of HDAC6 was profiled by using a panel of acyl derivatives of the optimized peptide substrate and showed that HDAC6 acts as a proficient deformylase. Our data thus offer a detailed insight into the substrate preferences of the individual HDAC6 domains at the peptide level, and these findings can in turn help in elucidating the biologic roles of the enzyme and facilitate the development of new domain-specific inhibitors as research tools or therapeutic agents.-Kutil, Z., Skultetyova, L., Rauh, D., Meleshin, M., Snajdr, I., Novakova, Z., Mikesova, J., Pavlicek, J., Hadzima, M., Baranova, P., Havlinova, B., Majer, P., Schutkowski, M., Barinka, C. The unraveling of substrate specificity of histone deacetylase 6 domains using acetylome peptide microarrays and peptide libraries.
Institute of Biotechnology of the Czech Academy of Sciences BIOCEV Vestec Czech Republic
Institute of Organic Chemistry and Biochemistry of the CAS Prague Czech Republic
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc20022857
- 003
- CZ-PrNML
- 005
- 20201214124902.0
- 007
- ta
- 008
- 201125s2019 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1096/fj.201801680R $2 doi
- 035 __
- $a (PubMed)30496698
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Kutil, Zsofia $u Institute of Biotechnology of the Czech Academy of Sciences, BIOCEV, Vestec, Czech Republic.
- 245 14
- $a The unraveling of substrate specificity of histone deacetylase 6 domains using acetylome peptide microarrays and peptide libraries / $c Z. Kutil, L. Skultetyova, D. Rauh, M. Meleshin, I. Snajdr, Z. Novakova, J. Mikesova, J. Pavlicek, M. Hadzima, P. Baranova, B. Havlinova, P. Majer, M. Schutkowski, C. Barinka,
- 520 9_
- $a Histone deacetylase 6 (HDAC6) is a multidomain cytosolic hydrolase acting mostly on nonhistone protein substrates. Investigations of the substrate specificity of HDAC6 are confounded by the presence of 2 catalytically active deacetylase domains (DD1 and DD2). In this study, acetylome peptide microarrays and peptide libraries were used to map the substrate specificity of DD1 and DD2 of human HDAC6. The results show that DD1 is solely responsible for the deacetylation of substrates harboring the acetyllysine at their C terminus, whereas DD2 exclusively deacetylates peptides with an internal acetyllysine residue. Also, statistical analysis of the deacetylation data revealed amino acid preferences at individual positions flanking the acetyllysine, where glycine and arginine residues are favored at positions N-terminal to the central acetyllysine; negatively charged glutamate is strongly disfavored throughout the sequence. Finally, the deacylation activity of HDAC6 was profiled by using a panel of acyl derivatives of the optimized peptide substrate and showed that HDAC6 acts as a proficient deformylase. Our data thus offer a detailed insight into the substrate preferences of the individual HDAC6 domains at the peptide level, and these findings can in turn help in elucidating the biologic roles of the enzyme and facilitate the development of new domain-specific inhibitors as research tools or therapeutic agents.-Kutil, Z., Skultetyova, L., Rauh, D., Meleshin, M., Snajdr, I., Novakova, Z., Mikesova, J., Pavlicek, J., Hadzima, M., Baranova, P., Havlinova, B., Majer, P., Schutkowski, M., Barinka, C. The unraveling of substrate specificity of histone deacetylase 6 domains using acetylome peptide microarrays and peptide libraries.
- 650 12
- $a katalytická doména $7 D020134
- 650 _2
- $a HEK293 buňky $7 D057809
- 650 _2
- $a histondeacetylasa 6 $x chemie $x metabolismus $7 D000073864
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a lysin $x chemie $x metabolismus $7 D008239
- 650 _2
- $a peptidové fragmenty $x chemie $x metabolismus $7 D010446
- 650 _2
- $a vazba proteinů $7 D011485
- 650 _2
- $a statická elektřina $7 D055672
- 650 _2
- $a substrátová specifita $7 D013379
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Skultetyova, Lubica $u Institute of Biotechnology of the Czech Academy of Sciences, BIOCEV, Vestec, Czech Republic.
- 700 1_
- $a Rauh, David $u Department of Enzymology, Charles Tanford Protein Center, Institute for Biochemistry and Biotechnology, Martin Luther University, Halle (Saale), Germany; and.
- 700 1_
- $a Meleshin, Marat $u Department of Enzymology, Charles Tanford Protein Center, Institute for Biochemistry and Biotechnology, Martin Luther University, Halle (Saale), Germany; and.
- 700 1_
- $a Snajdr, Ivan $u Institute of Organic Chemistry and Biochemistry of the CAS, Prague, Czech Republic.
- 700 1_
- $a Novakova, Zora $u Institute of Biotechnology of the Czech Academy of Sciences, BIOCEV, Vestec, Czech Republic.
- 700 1_
- $a Mikesova, Jana $u Institute of Biotechnology of the Czech Academy of Sciences, BIOCEV, Vestec, Czech Republic.
- 700 1_
- $a Pavlicek, Jiri $u Institute of Biotechnology of the Czech Academy of Sciences, BIOCEV, Vestec, Czech Republic.
- 700 1_
- $a Hadzima, Martin $u Institute of Organic Chemistry and Biochemistry of the CAS, Prague, Czech Republic.
- 700 1_
- $a Baranova, Petra $u Institute of Biotechnology of the Czech Academy of Sciences, BIOCEV, Vestec, Czech Republic.
- 700 1_
- $a Havlinova, Barbora $u Institute of Biotechnology of the Czech Academy of Sciences, BIOCEV, Vestec, Czech Republic.
- 700 1_
- $a Majer, Pavel $u Institute of Organic Chemistry and Biochemistry of the CAS, Prague, Czech Republic.
- 700 1_
- $a Schutkowski, Mike $u Department of Enzymology, Charles Tanford Protein Center, Institute for Biochemistry and Biotechnology, Martin Luther University, Halle (Saale), Germany; and.
- 700 1_
- $a Barinka, Cyril $u Institute of Biotechnology of the Czech Academy of Sciences, BIOCEV, Vestec, Czech Republic.
- 773 0_
- $w MED00001782 $t FASEB journal : official publication of the Federation of American Societies for Experimental Biology $x 1530-6860 $g Roč. 33, č. 3 (2019), s. 4035-4045
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/30496698 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20201125 $b ABA008
- 991 __
- $a 20201214124902 $b ABA008
- 999 __
- $a ok $b bmc $g 1595176 $s 1113533
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2019 $b 33 $c 3 $d 4035-4045 $e 20181129 $i 1530-6860 $m The FASEB journal $n FASEB J $x MED00001782
- LZP __
- $a Pubmed-20201125