Literature DB >> 10318849

Photoaffinity labeling and mass spectrometry identify ribosomal protein S3 as a potential target for hybrid polar cytodifferentiation agents.

Y Webb1, X Zhou, L Ngo, V Cornish, J Stahl, H Erdjument-Bromage, P Tempst, R A Rifkind, P A Marks, R Breslow, V M Richon.   

Abstract

The ability of a novel class of hybrid polar compounds (HPCs) to induce differentiation and consequent cessation of proliferation of transformed cells has led to their development as potential chemotherapeutic agents in the treatment of cancer. Suberoylanilide hydroxamic acid (SAHA) is a prototype of a family of hydroxamic acid based compounds (SAHA-like HPCs) that can, at micromolar concentrations, induce a variety of transformed cell lines to differentiate. The mechanism of action of the HPCs is not entirely understood. Searching for a cellular target of the SAHA-like HPCs, we synthesized a photoaffinity labeling reagent structurally based on SAHA, and probed for SAHA-binding proteins in murine erythroleukemia (MEL) cells. Photoaffinity labeling in cell free extracts identified a 32-kDa protein (p32) that was specifically labeled by the photoaffinity reagent. Cell fractionation assays localized p32 to the P100 fraction. p32 was partially purified and identified by mass spectrometry as the 40 S ribosomal protein S3. Expression of epitope-tagged S3 in bacterial lysates followed by photoaffinity labeling confirmed its specific labeling. Identification of a cytodifferentiation agent target may shed light on the mechanism by which the SAHA-like HPCs exert their antitumor effects.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10318849     DOI: 10.1074/jbc.274.20.14280

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  11 in total

1.  A new crosslinker for mass spectrometric analysis of the quaternary structure of protein complexes.

Authors:  J W Back; A F Hartog; H L Dekker; A O Muijsers; L J de Koning; L de Jong
Journal:  J Am Soc Mass Spectrom       Date:  2001-02       Impact factor: 3.109

2.  Identification of a transcriptional repressor related to the noncatalytic domain of histone deacetylases 4 and 5.

Authors:  X Zhou; V M Richon; R A Rifkind; P A Marks
Journal:  Proc Natl Acad Sci U S A       Date:  2000-02-01       Impact factor: 11.205

Review 3.  Photoaffinity labeling combined with mass spectrometric approaches as a tool for structural proteomics.

Authors:  David Robinette; Nouri Neamati; Kenneth B Tomer; Christoph H Borchers
Journal:  Expert Rev Proteomics       Date:  2006-08       Impact factor: 3.940

4.  Activity-based probes for proteomic profiling of histone deacetylase complexes.

Authors:  Cleo M Salisbury; Benjamin F Cravatt
Journal:  Proc Natl Acad Sci U S A       Date:  2007-01-16       Impact factor: 11.205

Review 5.  Chalcone: A Privileged Structure in Medicinal Chemistry.

Authors:  Chunlin Zhuang; Wen Zhang; Chunquan Sheng; Wannian Zhang; Chengguo Xing; Zhenyuan Miao
Journal:  Chem Rev       Date:  2017-05-10       Impact factor: 60.622

6.  Histone deacetylase 4 associates with extracellular signal-regulated kinases 1 and 2, and its cellular localization is regulated by oncogenic Ras.

Authors:  X Zhou; V M Richon; A H Wang; X J Yang; R A Rifkind; P A Marks
Journal:  Proc Natl Acad Sci U S A       Date:  2000-12-19       Impact factor: 11.205

7.  The antitumor histone deacetylase inhibitor suberoylanilide hydroxamic acid exhibits antiinflammatory properties via suppression of cytokines.

Authors:  Flavio Leoni; Andrea Zaliani; Giorgio Bertolini; Giulia Porro; Paolo Pagani; Pietro Pozzi; Giancarlo Donà; Gianluca Fossati; Silvano Sozzani; Tania Azam; Philip Bufler; Giamila Fantuzzi; Igor Goncharov; Soo-Hyun Kim; Benjamin J Pomerantz; Leonid L Reznikov; Britta Siegmund; Charles A Dinarello; Paolo Mascagni
Journal:  Proc Natl Acad Sci U S A       Date:  2002-02-26       Impact factor: 11.205

8.  Efficient identification of photolabelled amino acid residues by combining immunoaffinity purification with MS: revealing the semotiadil-binding site and its relevance to binding sites for myristates in domain III of human serum albumin.

Authors:  Kohichi Kawahara; Akihiko Kuniyasu; Katsuyoshi Masuda; Masaji Ishiguro; Hitoshi Nakayama
Journal:  Biochem J       Date:  2002-04-15       Impact factor: 3.857

9.  A photoactive isoprenoid diphosphate analogue containing a stable phosphonate linkage: synthesis and biochemical studies with prenyltransferases.

Authors:  Amanda J DeGraw; Zongbao Zhao; Corey L Strickland; A Huma Taban; John Hsieh; Michael Jefferies; Wenshuang Xie; David K Shintani; Colleen M McMahan; Katrina Cornish; Mark D Distefano
Journal:  J Org Chem       Date:  2007-05-04       Impact factor: 4.354

Review 10.  Photoaffinity labeling in target- and binding-site identification.

Authors:  Ewan Smith; Ian Collins
Journal:  Future Med Chem       Date:  2015       Impact factor: 3.808

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.