Building up PtII−Thiosemicarbazone−Lysine−sC18 Conjugates

Three chiral tridentate N^N^S coordinating pyridine‐carbaldehyde (S)‐N4‐(α‐methylbenzyl)thiosemicarbazones (HTSCmB) were synthesised along with lysine‐modified derivatives. One of them was selected and covalently conjugated to the cell‐penetrating peptide sC18 by solid‐phase peptide synthesis. The H...

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Vydané v:Chembiochem : a European journal of chemical biology Ročník 22; číslo 4; s. 694 - 704
Hlavní autori: Haseloer, Alexander, Lützenburg, Tamara, Strache, Joss Pepe, Neudörfl, Jörg, Neundorf, Ines, Klein, Axel
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: WEINHEIM Wiley 15.02.2021
Wiley Subscription Services, Inc
John Wiley and Sons Inc
Predmet:
Antiproliferative
Biochemistry & Molecular Biology
Biological activity
Cell lines
Cell viability
cell-penetrating peptides
Chemistry, Medicinal
Conjugates
Coordination compounds
Derivatives
Infrared spectroscopy
Labeling
Life Sciences & Biomedicine
Ligands
Lysine
NMR
Nuclear magnetic resonance
Nuclear medicine
Peptide synthesis
Peptides
Pharmacology & Pharmacy
platinum
Pyridines
Radioisotopes
Science & Technology
System effectiveness
thiosemicarbazone
Antiproliferative
ANTIPROLIFERATIVE ACTIVITY
PLATINUM(II) COMPLEXES
CRYSTAL-STRUCTURE
ANTITUMOR-ACTIVITY
CYTOTOXIC ACTIVITY
PEPTIDE
PALLADIUM(II) COMPLEXES
platinum
conjugates
cell-penetrating peptides
BIS(THIOSEMICARBAZONE) COMPLEXES
thiosemicarbazone
BASIS-SETS
ISSN:1439-4227, 1439-7633, 1439-7633
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Popis
Shrnutí:Three chiral tridentate N^N^S coordinating pyridine‐carbaldehyde (S)‐N4‐(α‐methylbenzyl)thiosemicarbazones (HTSCmB) were synthesised along with lysine‐modified derivatives. One of them was selected and covalently conjugated to the cell‐penetrating peptide sC18 by solid‐phase peptide synthesis. The HTSCmB model ligands, the HTSCLp derivatives and the peptide conjugate rapidly and quantitatively form very stable PtII chlorido complexes [Pt(TSC)Cl] when treated with K2PtCl4 in solution. The Pt(CN) derivatives were obtained from one TSCmB model complex and the peptide conjugate complex through Cl−→CN− exchange. Ligands and complexes were characterised by NMR, IR spectroscopy, HR‐ESI‐MS and single‐crystal XRD. Intriguingly, no decrease in cell viability was observed when testing the biological activity of the lysine‐tagged HdpyTSCLp, its sC18 conjugate HdpyTSCL‐sC18 or the PtCl and Pt(CN) conjugate complexes in three different cell lines. Thus, given the facile and effective preparation of such Pt‐TSC‐peptide conjugates, these systems might pave the way for future use in late‐stage labelling with Pt radionuclides and application in nuclear medicine. Late‐stage labelling: Chiral pyridine‐carbaldehyde (S)‐N4‐(α‐methylbenzyl)thiosemicarbazones were lysine modified (TSCLp) and covalently conjugated to the cell‐penetrating peptide sC18 by SPPS. Very stable PtII complexes [Pt(TSC)X] (X=Cl or CN) were synthesised, and the biological activity of the TSCLp, conjugate TSCL‐sC18, or Pt conjugate complexes was studied.
Bibliografia:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ISSN:1439-4227
1439-7633
1439-7633
DOI:10.1002/cbic.202000564