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Type: Journal article
Title: Rapid optimization of a peptide inhibitor of malaria parasite invasion by comprehensive N-methyl scanning
Author: Harris, K.
Casey, J.
Coley, A.
Karas, J.
Sabo, J.
Tan, Y.
Dolezal, O.
Norton, R.
Hughes, A.
Scanlon, D.
Foley, M.
Citation: Journal of Biological Chemistry, 2009; 284(14):9361-9371
Publisher: Amer Soc Biochemistry Molecular Biology Inc
Issue Date: 2009
ISSN: 0021-9258
Statement of
Karen S. Harris, Joanne L. Casey, Andrew M. Coley, John A. Karas, Jennifer K. Sabo, Yen Yee Tan, Olan Dolezal, Raymond S. Norton, Andrew B. Hughes, Denis Scanlon, and Michael Foley
Abstract: Apical membrane antigen 1 (AMA1) of the malaria parasite Plasmodium falciparum has been implicated in the invasion of host erythrocytes and is an important vaccine candidate. We have previously described a 20-residue peptide, R1, that binds to AMA1 and subsequently blocks parasite invasion. Because this peptide appears to target a site critical for AMA1 function, it represents an important lead compound for anti-malarial drug development. However, the effectiveness of this peptide inhibitor was limited to a subset of parasite isolates, indicating a requirement for broader strain specificity. Furthermore, a barrier to the utility of any peptide as a potential therapeutic is its susceptibility to rapid proteolytic degradation. In this study, we sought to improve the proteolytic stability and AMA1 binding properties of the R1 peptide by systematic methylation of backbone amides (N-methylation). The inclusion of a single N-methyl group in the R1 peptide backbone dramatically increased AMA1 affinity, bioactivity, and proteolytic stability without introducing global structural alterations. In addition, N-methylation of multiple R1 residues further improved these properties. Therefore, we have shown that modifications to a biologically active peptide can dramatically enhance activity. This approach could be applied to many lead peptides or peptide therapeutics to simultaneously optimize a number of parameters.
Keywords: Animals; Plasmodium falciparum; Peptides; Antimalarials; Nuclear Magnetic Resonance, Biomolecular; Surface Plasmon Resonance; Amino Acid Sequence; Substrate Specificity; Methylation; Time Factors; Molecular Sequence Data
Rights: © 2009 by The American Society for Biochemistry and Molecular Biology, Inc.
RMID: 0020106229
DOI: 10.1074/jbc.M808762200
Appears in Collections:Medical Sciences publications

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