Literature DB >> 18295503

Optimized sample preparation for MALDI mass spectrometry analysis of protected synthetic peptides.

Audrey M Schaiberger1, Jason A Moss.   

Abstract

The recent development and commercialization of Fuzeon (enfuvirtide) demonstrated that a convergent strategy comprised of both solid- and solution-phase synthetic methodologies presents a viable route for peptide manufacturing on a multi-ton scale. In this strategy, the target sequence is prepared by stepwise solid-phase synthesis of protected peptide fragments, which are then coupled together in the solution-phase to give the full-length sequence. These synthetic methodologies pose a unique challenge for mass spectrometry (MS), as protected peptide intermediates are often marked by poor solubility, structural lability, and low ionization potential. Matrix-assisted laser desorption/ionization (MALDI) MS is uniquely suited to such analytes; however, generalized protocols for MALDI analysis of protected peptides have yet to be demonstrated. Herein, we report an operationally simple sample preparation method for MALDI analysis of protected peptides, which greatly facilitates the collection and interpretation of MS data. In this method, the difficulty in MS analysis of protected peptides has been greatly diminished by use of dithranol as a matrix and CsCl as an additive, giving rise to intentionally-formed Cs(+) adducts. With greatly reduced fragmentation, better crystalline morphology, and easier data interpretation, we anticipate that these findings will find utility in peptide process development and manufacturing settings for reaction monitoring, troubleshooting, and quality control.

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Year:  2008        PMID: 18295503     DOI: 10.1016/j.jasms.2008.01.010

Source DB:  PubMed          Journal:  J Am Soc Mass Spectrom        ISSN: 1044-0305            Impact factor:   3.109


  16 in total

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Journal:  Anal Chem       Date:  2001-10-15       Impact factor: 6.986

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4.  Evaluation of matrix-assisted laser desorption ionization mass spectrometry for polymer characterization.

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Journal:  J Am Soc Mass Spectrom       Date:  1996-01       Impact factor: 3.109

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Authors:  S F Macha; P A Limbach; S D Hanton; K G Owens
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3.  Polymer End Group Control through a Decarboxylative Cobalt-Mediated Radical Polymerization: New Avenues for Synthesizing Peptide, Protein, and Nanomaterial Conjugates.

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