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Mapping small molecule binding sites with phage display technology / Lee Makowski.

Henry Stewart Biomedical & Life Sciences Collection Available online

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Format:
Video
Author/Creator:
Makowski, Lee, speaker, author.
Series:
Henry Stewart talks. Biomedical & life sciences collection. Chemical biology : the role of chemistry in our fundamental understanding of biology.
Chemical biology : the role of chemistry in our fundamental understanding of biology, 2056-452X
Language:
English
Subjects (All):
Biology.
Chemistry.
Medical Subjects:
Biology.
Chemistry.
Genre:
Video recordings.
Physical Description:
1 online resource (1 streaming video file (39 min.)) : color, sound.
polychrome
Place of Publication:
London : Henry Stewart Talks, 2008.
System Details:
Mode of access: World Wide Web.
video file
Contents:
Contents: How do you identify the molecular target of a small molecule drug?
Flexible regions are key players
P-loop of ATP-binding proteins is an important example
Can display libraries of flexible peptides on proteins select those that bind to the ligand
Selection is through an affinity process called biopanning
Success depends on the diversity of the library
Diversity depends on how many different peptides are in the library and their relative abundance
RELIC can be used to calculate the diversity of a library from the sequences of ~100 peptides
Identification of motifs from a population is easy if the motif is very strong
Taxol-binding peptides were also identified by phage display and those peptides were used to identify the position on tubulin where taxol is bound and to identify Bcl-2 as a taxolbinding protein
Significant data from a variety of sources argue that the taxol-Bcl-2 interaction is important to the clinical efficacy of taxol.
Notes:
Animated audio-visual presentation with synchronized narration.
Title from title frames.
Publisher Number:
1717 Henry Stewart Talks
Access Restriction:
Restricted for use by site license.

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