Hauptseite > Publikationsdatenbank > High-affinity binding and catalytic activity of His/Tyr-based sequences: Extending heme-regulatory motifs beyond CP > print |
001 | 889869 | ||
005 | 20210208142356.0 | ||
024 | 7 | _ | |a 10.1016/j.bbagen.2020.129603 |2 doi |
024 | 7 | _ | |a 0304-4165 |2 ISSN |
024 | 7 | _ | |a 1872-8006 |2 ISSN |
024 | 7 | _ | |a 32234408 |2 pmid |
024 | 7 | _ | |a WOS:000536132200008 |2 WOS |
037 | _ | _ | |a FZJ-2021-00477 |
082 | _ | _ | |a 610 |
100 | 1 | _ | |a Syllwasschy, Benjamin Franz |0 P:(DE-HGF)0 |b 0 |
245 | _ | _ | |a High-affinity binding and catalytic activity of His/Tyr-based sequences: Extending heme-regulatory motifs beyond CP |
260 | _ | _ | |a Amsterdam [u.a.] |c 2020 |b Elsevier |
336 | 7 | _ | |a article |2 DRIVER |
336 | 7 | _ | |a Output Types/Journal article |2 DataCite |
336 | 7 | _ | |a Journal Article |b journal |m journal |0 PUB:(DE-HGF)16 |s 1611321128_26190 |2 PUB:(DE-HGF) |
336 | 7 | _ | |a ARTICLE |2 BibTeX |
336 | 7 | _ | |a JOURNAL_ARTICLE |2 ORCID |
336 | 7 | _ | |a Journal Article |0 0 |2 EndNote |
500 | _ | _ | |a Kein Post-print verfügbar |
520 | _ | _ | |a Background & motivationPeptides and proteins can interact with heme through His, Tyr, or Cys in heme-regulatory motifs (HRMs). The Cys-Pro dipeptide is a well investigated HRM, but for His and Tyr such a distinct motif is currently unknown. In addition, many heme-peptide complexes, such as heme-amyloid β, can display a peroxidase-like activity, albeit there is little understanding of how the local primary and secondary coordination environment influences catalytic activity. We thus systematically evaluated a series of His- and Tyr-based peptides to identify sequence features for high-affinity heme binding and their impact on the catalytic activity of heme.MethodsWe employed solid-phase peptide synthesis to produce 58 nonapeptides, which were investigated by UV/vis, resonance Raman, and 2D NMR spectroscopy. A chromogenic assay was used to determine the catalytic activity of the heme-peptide complexes.ResultsHeme-binding affinity and binding mode were found to be dependent on the coordinating amino acid and spacer length between multiple potential coordination sites in a motif. In particular, HXH and HXXXH motifs showed strong heme binding. Analysis of the peroxidase-like activity revealed that some of these peptides and also HXXXY motifs enhance the catalytic activity of heme significantly.ConclusionsWe identify HXH, HXXXH, and HXXXY as potential new HRMs with functional properties. Several peptides displayed a strikingly high peroxidase-like activity.General significanceThe identification of HRMs allows to discover yet unknown heme-regulated proteins, and consequently, enhances our current understanding of pathologies involving labile heme. |
536 | _ | _ | |a 552 - Engineering Cell Function (POF3-552) |0 G:(DE-HGF)POF3-552 |c POF3-552 |f POF III |x 0 |
588 | _ | _ | |a Dataset connected to CrossRef |
700 | 1 | _ | |a Beck, Maximilian Steve |0 P:(DE-HGF)0 |b 1 |
700 | 1 | _ | |a Družeta, Ivona |0 P:(DE-HGF)0 |b 2 |
700 | 1 | _ | |a Hopp, Marie-Thérèse |0 P:(DE-HGF)0 |b 3 |
700 | 1 | _ | |a Ramoji, Anuradha |0 P:(DE-HGF)0 |b 4 |
700 | 1 | _ | |a Neugebauer, Ute |0 P:(DE-HGF)0 |b 5 |
700 | 1 | _ | |a Nozinovic, Senada |0 P:(DE-HGF)0 |b 6 |
700 | 1 | _ | |a Menche, Dirk |0 P:(DE-HGF)0 |b 7 |
700 | 1 | _ | |a Willbold, Dieter |0 P:(DE-Juel1)132029 |b 8 |u fzj |
700 | 1 | _ | |a Ohlenschläger, Oliver |0 P:(DE-HGF)0 |b 9 |
700 | 1 | _ | |a Kühl, Toni |0 P:(DE-HGF)0 |b 10 |
700 | 1 | _ | |a Imhof, Diana |0 P:(DE-HGF)0 |b 11 |e Corresponding author |
773 | _ | _ | |a 10.1016/j.bbagen.2020.129603 |g Vol. 1864, no. 7, p. 129603 - |0 PERI:(DE-600)2209617-6 |n 7 |p 129603 - |t Biochimica et biophysica acta / General subjects |v 1864 |y 2020 |x 0304-4165 |
856 | 4 | _ | |u https://juser.fz-juelich.de/record/889869/files/High-affinity%20binding%20and%20catalytic%20activity%20of%20HisTyr-based%20sequences_Extending%20heme-regulatory%20motifs%20beyond%20CP-1.pdf |y Restricted |
909 | C | O | |o oai:juser.fz-juelich.de:889869 |p VDB |
910 | 1 | _ | |a Forschungszentrum Jülich |0 I:(DE-588b)5008462-8 |k FZJ |b 8 |6 P:(DE-Juel1)132029 |
913 | 1 | _ | |a DE-HGF |b Key Technologies |l BioSoft – Fundamentals for future Technologies in the fields of Soft Matter and Life Sciences |1 G:(DE-HGF)POF3-550 |0 G:(DE-HGF)POF3-552 |3 G:(DE-HGF)POF3 |2 G:(DE-HGF)POF3-500 |4 G:(DE-HGF)POF |v Engineering Cell Function |x 0 |
914 | 1 | _ | |y 2020 |
915 | _ | _ | |a Nationallizenz |0 StatID:(DE-HGF)0420 |2 StatID |d 2020-09-12 |w ger |
915 | _ | _ | |a JCR |0 StatID:(DE-HGF)0100 |2 StatID |b BBA-GEN SUBJECTS : 2018 |d 2020-09-12 |
915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0200 |2 StatID |b SCOPUS |d 2020-09-12 |
915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0300 |2 StatID |b Medline |d 2020-09-12 |
915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0600 |2 StatID |b Ebsco Academic Search |d 2020-09-12 |
915 | _ | _ | |a Peer Review |0 StatID:(DE-HGF)0030 |2 StatID |b ASC |d 2020-09-12 |
915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0199 |2 StatID |b Clarivate Analytics Master Journal List |d 2020-09-12 |
915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)1030 |2 StatID |b Current Contents - Life Sciences |d 2020-09-12 |
915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0160 |2 StatID |b Essential Science Indicators |d 2020-09-12 |
915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)1050 |2 StatID |b BIOSIS Previews |d 2020-09-12 |
915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)1190 |2 StatID |b Biological Abstracts |d 2020-09-12 |
915 | _ | _ | |a WoS |0 StatID:(DE-HGF)0113 |2 StatID |b Science Citation Index Expanded |d 2020-09-12 |
915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0150 |2 StatID |b Web of Science Core Collection |d 2020-09-12 |
915 | _ | _ | |a IF < 5 |0 StatID:(DE-HGF)9900 |2 StatID |d 2020-09-12 |
920 | _ | _ | |l yes |
920 | 1 | _ | |0 I:(DE-Juel1)IBI-7-20200312 |k IBI-7 |l Strukturbiochemie |x 0 |
980 | _ | _ | |a journal |
980 | _ | _ | |a VDB |
980 | _ | _ | |a I:(DE-Juel1)IBI-7-20200312 |
980 | _ | _ | |a UNRESTRICTED |
Library | Collection | CLSMajor | CLSMinor | Language | Author |
---|