Literature DB >> 23088155

Studies toward the unique pederin family member psymberin: structure-activity relationships, biochemical studies, and genetics identify the mode-of-action of psymberin.

Cheng-Yang Wu1, Yu Feng, Eduardo R Cardenas, Noelle Williams, Paul E Floreancig, Jef K De Brabander, Michael G Roth.   

Abstract

Psymberin is the only member of the pederin natural product family that contains a dihydroisocoumarin side chain. Structural modifications of psymberin uncoupled inhibition of protein translation from cytotoxicity, suggesting that psymberin has more than one bioactivity. A forward genetic screen in Caenorhabditis elegans was conducted to identify the molecular target(s) of psymberin. Multiple independent psymberin-resistant mutants were isolated, each containing the same point mutation in a gene encoding a ribosomal protein. However, a psymberin-resistant mutant strain bearing this mutation was not cross-resistant to the pederin family member mycalamide A, which binds to the archaeal form of the same protein. Thus, two pederin family members likely differ in how they bind the same molecular target. The accumulation of psymberin in cells was sensitive to the stereochemistry of the amide side chain at C4 or C8 and the presence of the dihydroisocoumarin side chain. The observation that psymberin diastereomers or dihydroisocoumarin-truncated analogs lose all cytotoxic activity while retaining the ability to inhibit protein translation in a cell-free in vitro assay can be explained in the context of these differential cell uptake issues. Finally, we also demonstrate that the blistering activity associated with pederin and other members of the family is not due to their protein synthesis inhibiting activity. Unlike pederin and mycalamide, psymberin does not display irritant or blistering activity.

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Year:  2012        PMID: 23088155      PMCID: PMC3504174          DOI: 10.1021/ja3057002

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  23 in total

1.  Psymberin, a potent sponge-derived cytotoxin from Psammocinia distantly related to the pederin family.

Authors:  Robert H Cichewicz; Frederick A Valeriote; Phillip Crews
Journal:  Org Lett       Date:  2004-06-10       Impact factor: 6.005

2.  The in vitro biological activities of synthetic 18-O-methyl mycalamide B, 10-epi-18-O-methyl mycalamide B and pederin.

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Journal:  J Biol Chem       Date:  1969-08-25       Impact factor: 5.157

Review 4.  Exploring the chemistry of uncultivated bacterial symbionts: antitumor polyketides of the pederin family.

Authors:  Jörn Piel; Daniel Butzke; Nobuhiro Fusetani; Dequan Hui; Matthias Platzer; Gaiping Wen; Shigeki Matsunaga
Journal:  J Nat Prod       Date:  2005-03       Impact factor: 4.050

5.  Mycalamide D, a new cytotoxic amide from the New Zealand marine sponge Mycale species.

Authors:  L M West; P T Northcote; K A Hood; J H Miller; M J Page
Journal:  J Nat Prod       Date:  2000-05       Impact factor: 4.050

Review 6.  Finding function in novel targets: C. elegans as a model organism.

Authors:  Titus Kaletta; Michael O Hengartner
Journal:  Nat Rev Drug Discov       Date:  2006-05       Impact factor: 84.694

7.  Antitumor activity and mechanism of action of the novel marine natural products mycalamide-A and -B and onnamide.

Authors:  N S Burres; J J Clement
Journal:  Cancer Res       Date:  1989-06-01       Impact factor: 12.701

Review 8.  The mouse ear swelling test (MEST) in the 1990s.

Authors:  S C Gad
Journal:  Toxicology       Date:  1994-09-22       Impact factor: 4.221

9.  Studies toward the unique pederin family member psymberin: full structure elucidation, two alternative total syntheses, and analogs.

Authors:  Yu Feng; Xin Jiang; Jef K De Brabander
Journal:  J Am Chem Soc       Date:  2012-10-04       Impact factor: 15.419

10.  Studies on the mechanism of action of pederine.

Authors:  A Brega; A Falaschi; L De Carli; M Pavan
Journal:  J Cell Biol       Date:  1968-03       Impact factor: 10.539

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  8 in total

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2.  Asymmetric Synthesis of the C1-C6 Portion of the Psymberin Using an Evans Chiral Auxiliary.

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Journal:  Tetrahedron Lett       Date:  2013-10-09       Impact factor: 2.415

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4.  Design, Synthesis, and Evaluation of Irciniastatin Analogues: Simplification of the Tetrahydropyran Core and the C(11) Substituents.

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Review 5.  Predominately Uncultured Microbes as Sources of Bioactive Agents.

Authors:  David J Newman
Journal:  Front Microbiol       Date:  2016-11-18       Impact factor: 5.640

Review 6.  Contemporary Strategies for the Synthesis of Tetrahydropyran Derivatives: Application to Total Synthesis of Neopeltolide, a Marine Macrolide Natural Product.

Authors:  Haruhiko Fuwa
Journal:  Mar Drugs       Date:  2016-03-25       Impact factor: 5.118

7.  Targeted inhibitors of P-glycoprotein increase chemotherapeutic-induced mortality of multidrug resistant tumor cells.

Authors:  Amila K Nanayakkara; Courtney A Follit; Gang Chen; Noelle S Williams; Pia D Vogel; John G Wise
Journal:  Sci Rep       Date:  2018-01-17       Impact factor: 4.379

8.  Cu-catalyzed asymmetric addition of alcohols to β,γ-alkynyl-α-imino esters for the construction of linear chiral N,O-ketals.

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Journal:  Nat Commun       Date:  2022-01-20       Impact factor: 14.919

  8 in total

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