Literature DB >> 12627437

Physicochemical characterization of phosphinic pseudopeptides by capillary zone electrophoresis in highly acidic background electrolytes.

Dusan Koval1, Václav Kasicka, Jirí Jirácek, Michaela Collinsová.   

Abstract

Phosphinic pseudopeptides (i.e., peptide isosteres with one peptide bond replaced by a phosphinic acid moiety) were analyzed and physicochemically characterized by capillary zone electrophoresis in the pH range of 1.1-3.2, employing phosphoric, phosphinic, oxalic and dichloroacetic acids as background electrolyte (BGE) constituents. The acid dissociation constant (pK(a)) of phosphinate group in phosphinic pseudopeptides and ionic mobilities of these analytes were determined from the pH dependence of their effective electrophoretic mobilities corrected to standard temperature and constant ionic strength of the BGEs. It was shown that these corrections are necessary whenever precise mobility data at very low pH are to be determined. Additionally, it was found that the ionic mobilities of the phosphinic pseudopeptides and pK(a) of their phosphinate group are affected by the BGE constituent used. The variability of migration behavior of the pseudopeptides can be attributed to their ion-pairing formation with the BGE components.

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Year:  2003        PMID: 12627437     DOI: 10.1002/elps.200390097

Source DB:  PubMed          Journal:  Electrophoresis        ISSN: 0173-0835            Impact factor:   3.535


  3 in total

1.  Separation of peptide fragments of a protein kinase C substrate fused to a β-hairpin by capillary electrophoresis.

Authors:  Imola G Zigoneanu; Christopher E Sims; Nancy L Allbritton
Journal:  Anal Bioanal Chem       Date:  2015-10-01       Impact factor: 4.142

2.  S-alkylated homocysteine derivatives: new inhibitors of human betaine-homocysteine S-methyltransferase.

Authors:  Jiri Jiracek; Michaela Collinsova; Ivan Rosenberg; Milos Budesinsky; Eva Protivinska; Hana Netusilova; Timothy A Garrow
Journal:  J Med Chem       Date:  2006-06-29       Impact factor: 7.446

3.  Structure-activity study of new inhibitors of human betaine-homocysteine S-methyltransferase.

Authors:  Václav Vanek; Milos Budesínský; Petra Kabeleová; Miloslav Sanda; Milan Kozísek; Ivona Hanclová; Jana Mládková; Jirí Brynda; Ivan Rosenberg; Markos Koutmos; Timothy A Garrow; Jirí Jirácek
Journal:  J Med Chem       Date:  2009-06-25       Impact factor: 7.446

  3 in total

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