Focus on drug discovery
In This Issue - pv
doi:10.1038/nchembio1206-v
doi:10.1038/nchembio1206-645
Integrating chemistry and biology in the search for the next generation of therapeutics.
Full Text - Frontiers in drug discovery | PDF (76 KB) - Frontiers in drug discovery
Tomi K Sawyer
doi:10.1038/nchembio1206-646
By building on the successes of the past and leveraging both innovative technologies and predictive knowledge, scientists can develop smarter ways to create a molecular armamentarium of chemical and biological medicines.
Full Text - Smart drug discovery leveraging innovative technologies and predictive knowledge | PDF (1,319 KB) - Smart drug discovery leveraging innovative technologies and predictive knowledge
Nathanael S Gray
doi:10.1038/nchembio1206-649
Translational research in academia is extending beyond the traditional involvement in clinical trials to the early phases of the drug discovery process. Examples of successful academic-industrial partnerships illustrate the ways in which they can enable the discovery of new medicines.
Full Text - Drug discovery through industry-academic partnerships | PDF (377 KB) - Drug discovery through industry-academic partnerships
Joanne Kotz
doi:10.1038/nchembio1206-655
Seeking to maintain a supply of effective antibiotics, Stuart Levy combines research in microbiology and antibiotic drug discovery with a strong commitment to public communication.
Catherine Goodman
doi:10.1038/nchembio1206-657
As head of the Office of Orphan Products Development, Marlene Haffner offers a perspective on the immense influence the Orphan Drug Act has had in promoting research on and awareness of rare diseases.
Full Text - Marlene Haffner | PDF (259 KB) - Marlene Haffner
Philip J Hajduk
doi:10.1038/nchembio1206-658
Fragment-based drug design capitalizes on the modular binding of low-molecular-weight, low-affinity ligands. However, the deconstruction of lead-like inhibitors into putative fragments reveals the surprising complexity of dealing with low-affinity leads, thereby challenging oversimplification of these leads and highlighting the richness of their chemical diversity and molecular recognition.
Full Text - Puzzling through fragment-based drug design | PDF (311 KB) - Puzzling through fragment-based drug design
See also: Letter by Babaoglu & Shoichet
Byron R Griffith & Jon S Thorson
doi:10.1038/nchembio1206-659
Chemically synthesizing complex oligosaccharides remains a significant challenge. Through the addition of hydrophobic appendages to 'unnatural' substrates, some oligosaccharide-forming glycosyltransferases can direct the formation of distinct sugar linkages while maintaining stereoselectivity.
Full Text - A sweet success for substrate engineering | PDF (257 KB) - A sweet success for substrate engineering
See also: Letter by Lairson et al.
Jörn Piel
doi:10.1038/nchembio1206-661
Ascidians obtain diverse libraries of cytotoxic compounds by maintaining cyanobacterial symbionts that have combinatorial variants of a natural-product pathway. The biosynthetic flexibility of this route can be used to genetically engineer new substances.
Full Text - Combinatorial biosynthesis in symbiotic bacteria | PDF (152 KB) - Combinatorial biosynthesis in symbiotic bacteria
See also: Letter by Donia et al.
Stephen W Michnick
doi:10.1038/nchembio1206-663
The sheer quantity and complexity of gene expression data can provide extraordinarily accurate descriptions of differences between states of cells, tissues and whole organisms. A compendium of genomic signatures that attempts to describe all biological states has the potential to reveal hidden connections among drugs, genes and diseases.
Full Text - The connectivity map | PDF (240 KB) - The connectivity map
doi:10.1038/nchembio1206-665
Full Text - Research Highlights | PDF (274 KB) - Research Highlights
William Fenical & Paul R Jensen
doi:10.1038/nchembio841
Abstract - Developing a new resource for drug discovery: marine actinomycete bacteria | Full Text - Developing a new resource for drug discovery: marine actinomycete bacteria | PDF (479 KB) - Developing a new resource for drug discovery: marine actinomycete bacteria
Michelle C Y Chang & Jay D Keasling
doi:10.1038/nchembio836
Abstract - Production of isoprenoid pharmaceuticals by engineered microbes | Full Text - Production of isoprenoid pharmaceuticals by engineered microbes | PDF (287 KB) - Production of isoprenoid pharmaceuticals by engineered microbes
Sachdev S Sidhu & Frederic A Fellouse
doi:10.1038/nchembio843
Abstract - Synthetic therapeutic antibodies | Full Text - Synthetic therapeutic antibodies | PDF (2,054 KB) - Synthetic therapeutic antibodies | Supplementary information
Ian Collins & Paul Workman
doi:10.1038/nchembio840
Abstract - New approaches to molecular cancer therapeutics | Full Text - New approaches to molecular cancer therapeutics | PDF (2,647 KB) - New approaches to molecular cancer therapeutics
Adam R Renslo & James H McKerrow
doi:10.1038/nchembio837
Abstract - Drug discovery and development for neglected parasitic diseases | Full Text - Drug discovery and development for neglected parasitic diseases | PDF (314 KB) - Drug discovery and development for neglected parasitic diseases | Supplementary information
David Bumcrot, Muthiah Manoharan, Victor Koteliansky & Dinah W Y Sah
doi:10.1038/nchembio839
Abstract - RNAi therapeutics: a potential new class of pharmaceutical drugs | Full Text - RNAi therapeutics: a potential new class of pharmaceutical drugs | PDF (2,508 KB) - RNAi therapeutics: a potential new class of pharmaceutical drugs
Kerim Babaoglu & Brian K Shoichet
doi:10.1038/nchembio831

First Paragraph - Deconstructing fragment-based inhibitor discovery | Full Text - Deconstructing fragment-based inhibitor discovery | PDF (289 KB) - Deconstructing fragment-based inhibitor discovery | Supplementary information | Chemical compounds
See also: News and Views by Hajduk
Luke L Lairson, Andrew G Watts, Warren W Wakarchuk & Stephen G Withers
doi:10.1038/nchembio828

First Paragraph - Using substrate engineering to harness enzymatic promiscuity and expand biological catalysis | Full Text - Using substrate engineering to harness enzymatic promiscuity and expand biological catalysis | PDF (243 KB) - Using substrate engineering to harness enzymatic promiscuity and expand biological catalysis | Supplementary information | Chemical compounds
See also: News and Views by Griffith & Thorson
Mohamed S Donia, Brian J Hathaway, Sebastian Sudek, Margo G Haygood, M J Rosovitz, Jacques Ravel & Eric W Schmidt
doi:10.1038/nchembio829

First Paragraph - Natural combinatorial peptide libraries in cyanobacterial symbionts of marine ascidians | Full Text - Natural combinatorial peptide libraries in cyanobacterial symbionts of marine ascidians | PDF (364 KB) - Natural combinatorial peptide libraries in cyanobacterial symbionts of marine ascidians | Supplementary information | Chemical compounds
See also: News and Views by Piel
Nature Chemical Biology
ISSN: 1552-4450
EISSN: 1548-7105
