E. J. Mayer, E. McKenna, V. M. Garsky, C. J. Burke, H. Mach, C. R. Middaugh, M. Sardana, J. S. Smith and R.G. Johnson Jr., “Biochemical and Biophysical Comparison of Native and Chemically Synthesized Phospholamban and a Monomeric Phospholamban,” Journal of Biologyi-cal Chemistry, Vol. 271, 1996, pp. 1669-1677. doi10.1074/jbc.271.3.1669 - References

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E. J. Mayer, E. McKenna, V. M. Garsky, C. J. Burke, H. Mach, C. R. Middaugh, M. Sardana, J. S. Smith and R.G. Johnson Jr., “Biochemical and Biophysical Comparison of Native and Chemically Synthesized Phospholamban and a Monomeric Phospholamban,” Journal of Biologyi-cal Chemistry, Vol. 271, 1996, pp. 1669-1677. doi:10.1074/jbc.271.3.1669

has been cited by the following article:

TITLE: Improved Solid-Phase Peptide Synthesis of Wild-Type and Phosphorylated Phospholamban Using a Pseudoproline Dipeptide

AUTHORS: Shadi Abu-Baker, Gary A. Lorigan

KEYWORDS: Solid-State Peptide Synthesis; Pseudoproline Dipeptide; Phospholamban

JOURNAL NAME: Open Journal of Synthesis Theory and Applications, Vol.1 No.2, July 30, 2012

ABSTRACT: In this study, we report that the insertion of a pseudoproline dipeptide for the solid-phase peptide synthesis of wild-type Phospholamban protein (WT-PLB) has two important advantages. First, it disrupts the formation of different secondary structures, which is responsible for poor couplings during the preparation of highly aggregated sequences. Second, it enhances the purities and solubility of crude products leading to easier HPLC purification.