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dc.contributor.authorHolcombe, James A.
dc.contributor.authorStair, Jacqueline
dc.date.accessioned2013-04-08T14:29:39Z
dc.date.available2013-04-08T14:29:39Z
dc.date.issued2005-08
dc.identifier.citationHolcombe , J A & Stair , J 2005 , ' Metal remediation and preconcentration using immobilized short-chain peptides composed of aspartic acid and cysteine ' , Microchemical journal , vol. 81 , no. 1 , pp. 69-80 . https://doi.org/10.1016/j.microc.2005.01.003
dc.identifier.issn0026-265X
dc.identifier.urihttp://hdl.handle.net/2299/10325
dc.description.abstractShort-chain peptides (two and seven residues) consisting of a glycine (Gly) attachment group and various combinations of cysteine (Cys) and/or aspartic acid (Asp) were synthesized by Fmoc solid phase peptide synthesis (SPPS) on Tentagel resin. One selected peptide was synthesized on controlled pore glass (CPG) for comparison. The objective was to evaluate metal binding capacities and selectivities of short-chain peptides when minor alterations in the amino acid sequences were made. Metal binding of Ni2+, Cd2+, CO2+, and Mg2+ to the synthesized peptides was evaluated using breakthrough curves from a packed microcolumn and flame atomic absorption spectrophotometry (FAAS) detection. Peptides composed primarily of Asp showed single metal capacities as large as 720 mu mol metal/g Tentagel resin and 130 mu mol metal/g CPG. Simultaneous elution of a multi-metal solution demonstrated that peptides possessing only two Cys residues and four Asp residues were sufficient to yield selective binding of Cd2+ over Ni2+ and Co2+ similar to the selectivity of a six-Cys residue chain but with 60% more Cd2+ capacity. Interestingly, peptides supported on Tentagel resin appeared to reach equilibrium with metal-containing influent flow rates of at most 2 ml/min (or a linear velocity of 11 cm/s) and is attributed to better mass transport with the resin than with the CPG. Conditional stability constants calculated for the six-Asp residue chain and each metal showed the majority of sites having a log K in the range of 4.6-4.8. The peptides studied were also able to efficiently preconcentrate solutions containing as little as 0.05 mu g/ml Cd2+ or Ni2+ in an artificial seawater matrix. Uniquely, the seven residue peptides showed surprisingly high metal capacities and metal-to-residue binding ratios (reaching similar to 1:2),and are an order of magnitude better than results previously obtained for longer chain polyamino acids (50-70 residues) attached to CPG via silane chemistry. (c) 2005 Elsevier B.V All rights reserved.en
dc.format.extent12
dc.language.isoeng
dc.relation.ispartofMicrochemical journal
dc.subjectsolid phase peptide synthesis
dc.subjectaspartic acid
dc.subjectcysteine
dc.subjectglycine
dc.subjectTentagel resin
dc.subjectcontrolled pore glass
dc.subjection exchange
dc.subjectpreconcentration
dc.subjectremediation
dc.subjectmetal binding peptide
dc.subjectION-EXCHANGE
dc.subjectCOBALT(III) ION
dc.subjectSOLID SUPPORTS
dc.subjectGLUTAMIC ACID
dc.subjectCOMPLEXES
dc.subjectCHELATION
dc.subjectPOLY(L-CYSTEINE)
dc.subjectMETALLOPROTEINS
dc.subjectCOORDINATION
dc.subjectLIBRARIES
dc.titleMetal remediation and preconcentration using immobilized short-chain peptides composed of aspartic acid and cysteineen
dc.contributor.institutionSchool of Life and Medical Sciences
dc.contributor.institutionNanopharmaceutics
dc.contributor.institutionPsychopharmacology, Drug Misuse and Novel Psychoactive Substances Unit
dc.contributor.institutionCentre for Hazard Detection and Protection Research
dc.contributor.institutionCentre for Research in Mechanisms of Disease and Drug Discovery
dc.contributor.institutionDepartment of Clinical, Pharmaceutical and Biological Science
dc.contributor.institutionCentre for Health Services and Clinical Research
dc.description.statusPeer reviewed
rioxxterms.versionofrecord10.1016/j.microc.2005.01.003
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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