Dataset:
Potentiometric alkali titration data for the full tripeptide set composed from the combination of Glutamic acid (Glu, E), Glycine (Gly, G) and Histidine (His, H) with Copper (II) ions, measured between pH 3-12
Potentiometric alkali titration data for the full tripeptide set composed from the combination of Glutamic acid (Glu, E), Glycine (Gly, G) and Histidine (His, H) with Copper (II) ions, measured between pH 3-12
dc.contributor.other | Gloria, Danmar | en_US |
dc.contributor.other | Hibbert, Brynn | en_US |
dc.date.accessioned | 2021-11-26T10:32:33Z | |
dc.date.available | 2021-11-26T10:32:33Z | |
dc.date.issued | 2013 | en_US |
dc.description.abstract | Data type: ph Titration CurvesPeptides were purchased from Genosphere, Sigma Aldrich and Bachem companies. All the peptides were chemically synthesised. Aldrich and Bachem supplied the peptides as their Zwitterionic form, Genosphere synthesised the peptides as tri-fluoro acetic salt TFA salts. The peptides were of purity higher than 98% and were used without any further purification.All peptides solutions were prepared at 0.001M concentration in milliQ water, Hydrochloric acid HCl 0.002M in order to have relatively the same initial pH of 2.6 valueThe potentiometric titrations were recorded at 25°C in 10ml conical flask under Nitrogen atmosphere. NaCLO4 sodium perchlorate was used as ino background at 0.1M to maintain relatively a consistent ionic strength during titration. Standardised NaOH 0.1M was the titrant, and it was added as 5µM increment until pH reaches 11. Copper metal ion were initially added to the peptide solution at 0.001M in order to have a ligand metal ration of 1:1. | en_US |
dc.identifier.uri | http://hdl.handle.net/1959.4/004_340 | |
dc.language | English | |
dc.language.iso | EN | en_US |
dc.subject.other | Potentiometric Alkali titration | en_US |
dc.subject.other | Tripeptide acid disccociation constants | en_US |
dc.subject.other | Copper complexation with tripeptides and formation constants | en_US |
dc.subject.other | Tripeptides Glu, Gly, His | en_US |
dc.subject.other | Copper complexes speciation | en_US |
dc.title | Potentiometric alkali titration data for the full tripeptide set composed from the combination of Glutamic acid (Glu, E), Glycine (Gly, G) and Histidine (His, H) with Copper (II) ions, measured between pH 3-12 | en_US |
dc.type | Dataset | en_US |
dcterms.accessRights | metadata only access | |
dcterms.accrualMethod | http://hdl.handle.net/1959.4/004_128 | en_US |
dcterms.rightsHolder | Copyright 2012, University of New South Wales | en_US |
dspace.entity.type | Dataset | en_US |
unsw.accessRights.uri | http://purl.org/coar/access_right/c_14cb | |
unsw.contributor.leadChiefInvestigator | Raffoul Khoury, Rima | en_US |
unsw.contributor.researchDataCreator | Raffoul Khoury, Rima | en_US |
unsw.coverage.temporalFrom | 2009-07-01 | en_US |
unsw.coverage.temporalTo | 2010-12-31 | en_US |
unsw.description.contact | For access to this data, please contact Rima Raffoul Khoury; Room No. 121, Dalton Building, UNSW Australia; Email: rima_khoury2@hotmail.com | en_US |
unsw.description.storageplace | UNSW Australia, Sydney NSW 2052 | en_US |
unsw.identifier.doi | https://doi.org/10.26190/unsworks/1304 | |
unsw.relation.OriginalPublicationAffiliation | Gloria, Danmar, Division of Human Resources, Operations Division, | en_US |
unsw.relation.OriginalPublicationAffiliation | Hibbert, Brynn, School of Chemistry, Faculty of Science, | en_US |
unsw.relation.OriginalPublicationAffiliation | Raffoul Khoury, Rima, School of Chemistry, Faculty of Science, | en_US |
unsw.relation.faculty | Other UNSW | |
unsw.relation.faculty | Science | |
unsw.relation.projectDesc | For the first time, a complete systematic study of the reactions between Cu2+ and tripeptides containing glutamic acid (Glu, E), glycine (Gly, G), and histidine (His, H) is explored and reported in this thesis. This study revealed that the high-order interaction between the peptide residues is the major factor that controls peptide systems. The results of this project have implications in different fields including experimental design, multi-way data analysis, knowledge of peptide and metallo-peptide properties, and peptide-modified bio-sensors for copper sequestration. Potentiometric pH titration and visible spectroscopy were chosen as the most suitable analytical techniques for this purpose. The experiments provided data on acid dissociation constants (pKa), copper-complex formation constants (log?), copper speciation and their spectral parameters (maximum absorption wavelength) for the full tripeptide set. The quantum mechanical modelling method PM6 was used to optimise the geometry of copper complex species with the various tripeptides. The outputs provided information about the copper complex geometries, the peptide’s copper anchoring atoms and thus the copper binding mode. The optimised geometries were mostly distorted structures and varied between tetrahedral (or trigonal planar) and square planar shapes in which the copper was tetra-bound to the peptide via 3 or 4 nitrogen atoms (3N and 4N). The mathematical model generalized multiplicative analysis of variance (GEMANOVA) was used to perform multi-way modelling of the pKa and log? values determined by potentiometry. GEMANOVA generates parsimonious models of high-order interactions. For this reason, GEMANOVA models were used to explain and quantify the effects of the interactions between the positions and the kinds of the tripeptides residues on the magnitude of the pKa and log? values. Principal components analysis (PCA) and multivariate curve resolution–alternating least square (MCR-ALS) methods were used to decompose the spectroscopic data into their pure components. PCA and MCR-ALS were used to confirm the presence or absence of the copper complex species identified in the visible spectra including the bis-complex (metal:ligand 2:1) and dimer species (2:2) that can be formed with tripeptides containing His at N-terminus and central position. | en_US |
unsw.relation.projectEndDate | 2013-12-31 | en_US |
unsw.relation.projectStartDate | 2009-01-01 | en_US |
unsw.relation.projectTitle | Complete systematic study of reactions between copper(II) ions and tripeptides containing glutamic acid, glycine and histidine | en_US |
unsw.relation.school | School of Chemistry | |
unsw.relation.school | School of Chemistry | |
unsw.subject.fieldofresearchcode | 030107 Sensor Technology (Chemical aspects) | en_US |
unsw.subject.fieldofresearchcode | 030199 Analytical Chemistry not elsewhere classified | en_US |
unsw.subject.fieldofresearchcode | 030299 Inorganic Chemistry not elsewhere classified | en_US |
unsw.subject.fieldofresearchcode | 030604 Electrochemistry | en_US |
unsw.subject.fieldofresearchcode | 030799 Theoretical and Computational Chemistry not elsewhere classified | en_US |