36
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      A biocompatible condensation reaction for controlled assembly of nanostructures in live cells

      research-article
      1 , 1 , 1 , *
      Nature chemistry

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Through controlled synthesis and molecular assembly, biological systems are able to organize molecules into supramolecular structures that carry out sophisticated processes. Although chemists have reported a few examples of supramolecular assembly in water, the controlled covalent synthesis of large molecules and structures in vivo has remained challenging. Here we report a condensation reaction between 1,2-aminothiol and 2-cyanobenzothiazole that occurs in vitro and in living cells under the control of pH, disulfide reduction and enzymatic cleavage. In vitro, the size and shape of the condensation products, and nanostructures subsequently assembled, were different in each case and could thus be controlled by tuning the structure of the monomers. Direct imaging of the products obtained in the cells revealed their locations – near the Golgi bodies under enzymatic cleavage control – demonstrating the feasibility of a controlled and localized reaction in living cells. This intracellular condensation process enabled the imaging of the proteolytic activity of furin.

          Related collections

          Most cited references38

          • Record: found
          • Abstract: not found
          • Article: not found

          Click Chemistry: Diverse Chemical Function from a Few Good Reactions

            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Molecular self-assembly and nanochemistry: a chemical strategy for the synthesis of nanostructures

            Molecular self-assembly is the spontaneous association of molecules under equilibrium conditions into stable, structurally well-defined aggregates joined by noncovalent bonds. Molecular self-assembly is ubiquitous in biological systems and underlies the formation of a wide variety of complex biological structures. Understanding self-assembly and the associated noncovalent interactions that connect complementary interacting molecular surfaces in biological aggregates is a central concern in structural biochemistry. Self-assembly is also emerging as a new strategy in chemical synthesis, with the potential of generating nonbiological structures with dimensions of 1 to 10(2) nanometers (with molecular weights of 10(4) to 10(10) daltons). Structures in the upper part of this range of sizes are presently inaccessible through chemical synthesis, and the ability to prepare them would open a route to structures comparable in size (and perhaps complementary in function) to those that can be prepared by microlithography and other techniques of microfabrication.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Cell surface engineering by a modified Staudinger reaction.

              Selective chemical reactions enacted within a cellular environment can be powerful tools for elucidating biological processes or engineering novel interactions. A chemical transformation that permits the selective formation of covalent adducts among richly functionalized biopolymers within a cellular context is presented. A ligation modeled after the Staudinger reaction forms an amide bond by coupling of an azide and a specifically engineered triarylphosphine. Both reactive partners are abiotic and chemically orthogonal to native cellular components. Azides installed within cell surface glycoconjugates by metabolism of a synthetic azidosugar were reacted with a biotinylated triarylphosphine to produce stable cell-surface adducts. The tremendous selectivity of the transformation should permit its execution within a cell's interior, offering new possibilities for probing intracellular interactions.
                Bookmark

                Author and article information

                Journal
                101499734
                35773
                Nat Chem
                Nature chemistry
                1755-4330
                1755-4349
                2 October 2011
                January 2010
                18 October 2011
                : 2
                : 1
                : 54-60
                Affiliations
                [1 ]Molecular Imaging Program at Stanford, Departments of Radiology and Chemistry, Stanford University, 1201 Welch Road, Stanford, California 94305-5484, USA
                Author notes
                [* ]Correspondence should be addressed to J. R. ( jrao@ 123456stanford.edu )
                Article
                nihpa159164
                10.1038/nchem.480
                3196337
                21124381
                b8f4ba3c-7f72-454d-80b5-e729c5773405
                History
                Funding
                Funded by: National Institute of General Medical Sciences : NIGMS
                Award ID: R01 GM086196-01 || GM
                Categories
                Article

                Chemistry
                Chemistry

                Comments

                Comment on this article