selection of peptides targeting helix 31 of bacterial 16s ribosomal rna by screening m13 phage-display libraries选择针对螺旋肽31筛选细菌16 s rrna的m13噬菌体展示库.pdfVIP
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selection of peptides targeting helix 31 of bacterial 16s ribosomal rna by screening m13 phage-display libraries选择针对螺旋肽31筛选细菌16 s rrna的m13噬菌体展示库
Molecules 2011, 16, 1211-1239; doi:10.3390/molecule
OPEN ACCESS
molecules
ISSN 1420-3049
/journal/molecules
Article
Selection of Peptides Targeting Helix 31 of Bacterial 16S
Ribosomal RNA by Screening M13 Phage-Display Libraries
Tek N. Lamichhane 1,2,‡,†, N. Dinuka Abeydeera 1,§,†, Anne-Cécile E. Duc 1,||,
Philip R. Cunningham 2 and Christine S. Chow 1,*
1 Department of Chemistry, Wayne State University, Detroit, MI 48202, USA
2 Department of Biological Sciences, Wayne State University, Detroit, MI 48202, USA
‡ Current address: Intramural Research Program, NICHD, NIH, Bethesda, MD 20892, USA
§ Current address: Department of Chemistry, Texas AM University, College Station, TX 77843, USA
|| Current address: Immune Cell Development and Host Defense Program, Fox Chase Cancer Center,
333 Cottman Avenue, Philadelphia, PA 19111, USA
† These authors contributed equally to this work.
* Author to whom correspondence should be addressed; E-Mail: csc@;
Tel: +1-313-577-2594; Fax: +1-313-577-8822.
Received: 5 January 2011; in revised form : 24 January 2011 / Accepted: 25 January 2011 /
Published: 28 January 2011
Abstract: Ribosomal RNA is the catalytic portion of ribosomes, and undergoes a variety
of conformational changes during translation. Structural changes in ribosomal RNA can be
facilitated by the presence of modified nucleotides. Helix 31 of bacterial 16S ribosomal
2 5
RNA harbors two modified nucleotides, m G966 and m C967, that are highly conserved
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