TY - JOUR
T1 - Antimicrobial peptides in frog skin secretions.
AU - Conlon, J. Michael
AU - Sonnevend, Agnes
PY - 2010
Y1 - 2010
N2 - Skin secretions from many species of anurans (frogs and toads) are a rich source of peptides with broad-spectrum antimicrobial activities that may be developed into agents with therapeutic potential, particularly for topical applications. This chapter describes the use of norepinephrine (injection or immersion) to stimulate peptide release from granular glands in the skin in procedures that do not appear to cause distress to the animals. The peptide components in the secretions are separated using reversed-phase HPLC on octadecylsilyl-silica (C(18)) columns after partial purification on Sep-Pak C(18) cartridges. Peptides with antimicrobial activity are then identified by demonstration of their abilities to inhibit growth of Gram-negative (Escherichia coli) and Gram-positive (Staphylococcus aureus) bacteria in liquid phase microtiter plate assays. Individual peptides with activity are purified to near homogeneity by further chromatography on butylsilyl-(C(4)) and diphenylmethylsilyl-silica columns and characterized structurally by automated Edman degradation and mass spectrometry.
AB - Skin secretions from many species of anurans (frogs and toads) are a rich source of peptides with broad-spectrum antimicrobial activities that may be developed into agents with therapeutic potential, particularly for topical applications. This chapter describes the use of norepinephrine (injection or immersion) to stimulate peptide release from granular glands in the skin in procedures that do not appear to cause distress to the animals. The peptide components in the secretions are separated using reversed-phase HPLC on octadecylsilyl-silica (C(18)) columns after partial purification on Sep-Pak C(18) cartridges. Peptides with antimicrobial activity are then identified by demonstration of their abilities to inhibit growth of Gram-negative (Escherichia coli) and Gram-positive (Staphylococcus aureus) bacteria in liquid phase microtiter plate assays. Individual peptides with activity are purified to near homogeneity by further chromatography on butylsilyl-(C(4)) and diphenylmethylsilyl-silica columns and characterized structurally by automated Edman degradation and mass spectrometry.
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U2 - 10.1007/978-1-60761-594-1_1
DO - 10.1007/978-1-60761-594-1_1
M3 - Article
C2 - 20094854
AN - SCOPUS:77950471557
SN - 1064-3745
VL - 618
SP - 3
EP - 14
JO - Methods in molecular biology (Clifton, N.J.)
JF - Methods in molecular biology (Clifton, N.J.)
ER -