Literature DB >> 23975779

Design of transmembrane peptides: coping with sticky situations.

Arianna Rath1, Charles M Deber.   

Abstract

Membrane proteins have central roles in cellular processes ranging from nutrient uptake to cell-cell communication, and are key drug targets. However, research on α-helical integral membrane proteins is in its relative infancy vs. water-soluble proteins, largely because of their water insolubility when extracted from their native membrane environment. Peptides with sequences that correspond to the membrane-spanning segments of α-helical integral membrane proteins, termed transmembrane (TM) peptides, provide valuable tools for the characterization of these molecules. Here we describe in detail protocols for the design of TM peptides from the sequences of natural α-helical integral membrane proteins and outline strategies for their synthesis and for improving their solubility properties.

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Year:  2013        PMID: 23975779     DOI: 10.1007/978-1-62703-583-5_11

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  2 in total

1.  Sensitive Versatile Fluorogenic Transmembrane Peptide Substrates for Rhomboid Intramembrane Proteases.

Authors:  Anežka Tichá; Stancho Stanchev; Jan Škerle; Jakub Began; Marek Ingr; Kateřina Švehlová; Lucie Polovinkin; Martin Růžička; Lucie Bednárová; Romana Hadravová; Edita Poláchová; Petra Rampírová; Jana Březinová; Václav Kašička; Pavel Majer; Kvido Strisovsky
Journal:  J Biol Chem       Date:  2017-01-09       Impact factor: 5.157

2.  The transmembrane domains of the bacterial cell division proteins FtsB and FtsL form a stable high-order oligomer.

Authors:  Ambalika S Khadria; Alessandro Senes
Journal:  Biochemistry       Date:  2013-10-18       Impact factor: 3.162

  2 in total

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