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


LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21