Literature DB >> 18929455

The molecular descriptor logSumAA and its alternatives in QSRR models to predict the retention of peptides.

K Bodzioch1, T Baczek, R Kaliszan, Y Vander Heyden.   

Abstract

The use of the experimental molecular descriptor logSum(AA) and some possible alternatives were evaluated in the QSRR analysis of peptides. To quantitatively characterize the structure of analytes in a previously proposed QSRR the following three structural descriptors were applied: the logarithm of the sum of gradient retention times of the amino acids composing the individual peptide, logSum(AA); the logarithm of the peptide's van der Waals volume, logVDW(Vol); and the logarithm of its theoretically calculated n-octanol-water partition coefficient, clogP. Taking into consideration that most amino acids were hardly retained in the different RP-HPLC systems on which the peptides retention was measured, the contribution of most amino acids to the logSum(AA) descriptor is rather constant. Therefore, to enlarge the variability of the descriptor and the amino acids contributions for a given series of peptides, in a first instance, it was evaluated whether, by changing the chromatographic conditions, the retention differences between the amino acids could be increased, while maintaining their mutual selectivity. It was not evident to find such conditions. Secondly, it was also investigated whether the experimental descriptor logSum(AA) can be replaced by a theoretical, either based on a simple or on a weighted counting of the amino acids composing the peptide. The weighting factor for the retained amino acids was determined by their experimental gradient retention times measured on different systems. The predictive abilities of the new QSRR models (applying the alternative descriptors) were assessed using the leave-one-out cross-validation procedure and compared to that of the initial model. Finally, a descriptor was defined for which the retention measurement of only a limited number of amino acids is required. It resulted in QSRR models with similar predictive properties as those with logSum(AA), but with a reduced workload.

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Year:  2008        PMID: 18929455     DOI: 10.1016/j.jpba.2008.09.004

Source DB:  PubMed          Journal:  J Pharm Biomed Anal        ISSN: 0731-7085            Impact factor:   3.935


  3 in total

1.  Reversed-phase fused-core HPLC modeling of peptides.

Authors:  Matthias D'Hondt; Bert Gevaert; Sofie Stalmans; Sylvia Van Dorpe; Evelien Wynendaele; Kathelijne Peremans; Christian Burvenich; Bart De Spiegeleer
Journal:  J Pharm Anal       Date:  2012-11-30

2.  QSRR Modeling for Metabolite Standards Analyzed by Two Different Chromatographic Columns Using Multiple Linear Regression.

Authors:  Chrysostomi Zisi; Ioannis Sampsonidis; Stella Fasoula; Konstantinos Papachristos; Michael Witting; Helen G Gika; Panagiotis Nikitas; Adriani Pappa-Louisi
Journal:  Metabolites       Date:  2017-02-09

3.  Correctness of protein identifications of Bacillus subtilis proteome with the indication on potential false positive peptides supported by predictions of their retention times.

Authors:  Katarzyna Macur; Tomasz Baczek; Roman Kaliszan; Caterina Temporini; Federica Corana; Gabriella Massolini; Jolanta Grzenkowicz-Wydra; Michał Obuchowski
Journal:  J Biomed Biotechnol       Date:  2009-12-23
  3 in total

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