LL-37 is a recently described human antibacterial peptide that is constitutively present in human granulocytes and testis and is inducibly synthesized by human keratinocytes. This cationic, 37-amino acid peptide assumes an amphipathic a-helical conformation and is structurally distinct from all other antibacterial peptides heretofore identified in nature. The expression of the gene encoding LL-37 is induced in a number of skin inflammatory disorders and the peptide has been immunochemically localized throughout the epidermis in regions of inflamed but not normal skin(2). Hence, its presence in the epidermis of patients with skin disorders could represent an antimicrobial obstacle that bacterial pathogens would need to overcome to establish an infection. Very limited information is currently available regarding the antibacterial action of LL-37. It is the purpose of this pilot project to ascertain how its structure relates to its antimicrobial function. We will use synthetic peptide chemistry procedures to identify the amino acids of LL-37 needed for its broad-spectrum antibacterial action against two diverse bacterial that cause significant, serious skin infections.

Project Start
1998-03-01
Project End
1999-04-30
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
5
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Emory University
Department
Type
DUNS #
042250712
City
Atlanta
State
GA
Country
United States
Zip Code
30322
Arbiser, Jack L; Bonner, Michael Y; Gilbert, Linda C (2017) Targeting the duality of cancer. NPJ Precis Oncol 1:
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Laidlaw, Kamilla M E; Berhan, Samuel; Liu, Suhu et al. (2016) Cooperation of imipramine blue and tyrosine kinase blockade demonstrates activity against chronic myeloid leukemia. Oncotarget 7:51651-51664
Bhandarkar, Sulochana S; Lanka, Padmavathy; Lanka, Lakshmana Rao et al. (2016) Tuberculosis verrucosa cutis lesions exhibit a greater microvessel count than lupus vulgaris lesions. Exp Dermatol 25:479-80
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Bonner, Michael Y; Karlsson, Isabella; Rodolfo, Monica et al. (2016) Honokiol bis-dichloroacetate (Honokiol DCA) demonstrates activity in vemurafenib-resistant melanoma in vivo. Oncotarget 7:12857-68
Arbiser, Jack L; Bonner, Michael Y (2016) Seborrheic Keratoses: The Rodney Dangerfield of Skin lesions, and Why They Should Get Our Respect. J Invest Dermatol 136:564-566
Arbiser, Jack L (2014) PHIPing out: a genetic basis for tumor ulceration. J Invest Dermatol 134:600-602
Spence-Shishido, Allyson; Carr, Christopher; Bonner, Michael Y et al. (2013) In vivo Gram staining of tinea versicolor. JAMA Dermatol 149:991-2

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