Friday, February 15, 2013

Nature Chemical Biology Contents: March 2013 Volume 9 Number 3, pp 135 - 192

Nature Chemical Biology

TABLE OF CONTENTS

March 2013 Volume 9, Issue 3

Editorial
Correspondence
Research Highlights
News and Views
Review
Brief Communications
Articles
Addendum
Corrigendum
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Nature Reprint Collection on Epigenetics

This collection of articles focuses on histone methylation, its links to human disease and the development of chemical modulators of histone methylation states as leads for chromatin-targeted drug discovery.

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Editorial

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Authors on the record   p135
doi:10.1038/nchembio.1201
Publication of a paper initiates the process of scientific exchange that requires the ongoing participation of authors.

Correspondence

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Chaetocin is a nonspecific inhibitor of histone lysine methyltransferases   pp136 - 137
Fanny L Cherblanc, Kathryn L Chapman, Robert Brown and Matthew J Fuchter
doi:10.1038/nchembio.1187

See also: Correspondence by Greiner et al.

Reply to "Chaetocin is a nonspecific inhibitor of histone lysine methyltransferases"   p137
Dorothea Greiner, Tiziana Bonaldi, Ragnhild Eskeland, Ernst Roemer and Axel Imhof
doi:10.1038/nchembio.1188

See also: Correspondence by Cherblanc et al.

Research Highlights

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Cancer: Priority targets | Synthesis: A radical way of thinking | Photosynthesis: Elusive reductase found | Enzymes: Specificity swap | Antibiotic mechanisms: PAS is doubly poisonous | Pluripotency: Oleate dependency | Neurobiology: A pain paradox | Metabolism: AMPing up life

News and Views

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Receptors: Chemical courtship in mice   pp140 - 141
Charles W Luetje
doi:10.1038/nchembio.1180
Physiologically relevant ligands for mammalian odorant receptors have been elusive. A mouse odorant receptor-based bioassay has now been used to guide purification and identification of a natural ligand that mediates attraction of female mice to male urine.

See also: Brief Communication by Yoshikawa et al.

Protein-protein interactions: A PUMA mechanism unfolds   pp141 - 143
Loren D Walensky
doi:10.1038/nchembio.1177
PUMA is a BCL-2 family protein that transmits stress signals to promote apoptosis. Upon DNA damage, a unique binding determinant within PUMA triggers partial unfolding of BCL-XL, resulting in the release of sequestered p53 and commitment to p53-dependent cell death.

See also: Article by Follis et al.

Metalloenzymes: Cage redesign explains assembly   pp143 - 144
Elizabeth C Theil and Paola Turano
doi:10.1038/nchembio.1182
Control of protein self-assembly and disassembly, which is central to metabolism and engineering applications, remains challenging. Here, a perspicacious redesign of interfaces in the multisubunit ferritin protein cage provides single, modifiable subunits that assemble with Cu2+ templating and give insights into the cage assembly code.

See also: Article by Huard et al.

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Review

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Essential nontranslational functions of tRNA synthetases   pp145 - 153
Min Paul and Paul Schimmel
doi:10.1038/nchembio.1158



Beyond their canonical functions of charging tRNAs with amino acids for protein translation, tRNA synthetases have numerous nontranslational roles that regulate signaling, immunity and development.

Brief Communications

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A conserved asparagine has a structural role in ubiquitin-conjugating enzymes   pp154 - 156
Christopher E Berndsen, Reuven Wiener, Ian W Yu, Alison E Ringel and Cynthia Wolberger
doi:10.1038/nchembio.1159



Ubiquitin-conjugating (E2) enzymes contain a conserved asparagine that has been proposed to stabilize an oxyanion intermediate. Structural and biochemical studies of Ubc13 suggest that this residue has a structural role in stabilizing the E2 active site.

The sequence of the enterococcal cytolysin imparts unusual lanthionine stereochemistry   pp157 - 159
Weixin Tang and Wilfred A van der Donk
doi:10.1038/nchembio.1162



Heterologous expression of the two components of enterococcal cytolysin with a lanthionine synthetase enables the structural determination of this antimicrobial and hemolytic pair, revealing unexpected stereochemistry in one of the lanthionine bridges that is driven by peptide sequence.

An unsaturated aliphatic alcohol as a natural ligand for a mouse odorant receptor   pp160 - 162
Keiichi Yoshikawa, Hiroaki Nakagawa, Naoki Mori, Hidenori Watanabe and Kazushige Touhara
doi:10.1038/nchembio.1164



A natural aliphatic alcohol ligand of the mouse orphan odorant receptor Olfr288 from the male preputial gland is regulated by testosterone and affects attractiveness to female mice.
Chemical compounds
See also: News and Views by Luetje

Articles

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PUMA binding induces partial unfolding within BCL-xL to disrupt p53 binding and promote apoptosis   pp163 - 168
Ariele Viacava Follis, Jerry E Chipuk, John C Fisher, Mi-Kyung Yun, Christy R Grace, Amanda Nourse, Katherine Baran, Li Ou, Lie Min, Stephen W White, Douglas R Green and Richard W Kriwacki
doi:10.1038/nchembio.1166



π-stacking interactions unique between residues of PUMA and Bcl-xL, which lead to the unfolding of Bcl-xL via an allosteric mechanism, are required to disrupt p53–Bcl-xL interaction and induce apoptosis. This is the first example of regulated protein unfolding for signal transmission.

See also: News and Views by Walensky

Re-engineering protein interfaces yields copper-inducible ferritin cage assembly   pp169 - 176
Dustin J E Huard, Kathleen M Kane and F Akif Tezcan
doi:10.1038/nchembio.1163



A new protein engineering approach inserts metal-coordination motifs to stabilize natural protein interfaces while other favorable contacts are removed, yielding metal-inducible protein-protein interactions that have allowed the study of a self-assembling protein cage and the chemical labeling of its interior.

See also: News and Views by Theil & Turano

A new structural paradigm in copper resistance in Streptococcus pneumoniae    pp177 - 183
Yue Fu, Ho-Ching Tiffany Tsui, Kevin E Bruce, Lok-To Sham, Khadine A Higgins, John P Lisher, Krystyna M Kazmierczak, Michael J Maroney, Charles E Dann III, Malcolm E Winkler and David P Giedroc
doi:10.1038/nchembio.1168



Structural analyses reveal that CopA and CupA share a binuclear Cu(I) ion binding motif and that copper is trafficked from a low-affinity site on CupA to a high-affinity site in CopA, making CupA the first membrane-bound copper chaperone important in copper resistance.

Discovery of a chemical probe for the L3MBTL3 methyllysine reader domain   pp184 - 191
Lindsey I James, Dalia Barsyte-Lovejoy, Nan Zhong, Liubov Krichevsky, Victoria K Korboukh, J Martin Herold, Christopher J MacNevin, Jacqueline L Norris, Cari A Sagum, Wolfram Tempel, Edyta Marcon, Hongbo Guo, Cen Gao, Xi-Ping Huang, Shili Duan, Andrew Emili, Jack F Greenblatt, Dmitri B Kireev, Jian Jin, William P Janzen, Peter J Brown, Mark T Bedford, Cheryl H Arrowsmith and Stephen V Frye
doi:10.1038/nchembio.1157



Methylation of lysine residues regulates chromatin function in part by recruiting readers to these marks. UNC1215, a selective antagonist of the methyllysine reader L3MBTL3 with a polyvalent mode of interaction, reveals BCLAF1 as a methyllysine-dependent interaction partner for L3MBTL3.
Chemical compounds

Addendum

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Chemical inhibitor of nonapoptotic cell death with therapeutic potential for ischemic brain injury   p192
Alexei Degterev, Zhihong Huang, Michael Boyce, Yaqiao Li, Prakash Jagtap, Noboru Mizushima, Gregory D Cuny, Timothy J Mitchison, Michael A Moskowitz and Junying Yuan
doi:10.1038/nchembio0313-192a

Corrigendum

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Conformational stabilization of ubiquitin yields potent and selective inhibitors of USP7   p192
Yingnan Zhang, Lijuan Zhou, Lionel Rouge, Aaron H Phillips, Cynthia Lam, Peter Liu, Wendy Sandoval, Elizabeth Helgason, Jeremy M Murray, Ingrid E Wertz and Jacob E Corn
doi:10.1038/nchembio0313-192b

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1 comment:

Unknown said...

UNC1215 is a potent, selective antagonist of L3MBTL3 with cellular activity. UNC1215 has an IC50 of 20 nM and > 100-fold selectivity over 13 HMTs and selected representativ UNC1215