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一种生物相容性的缩合反应,可用于在活细胞中控制纳米结构的组装。

A biocompatible condensation reaction for controlled assembly of nanostructures in living cells.

机构信息

Molecular Imaging Program at Stanford, Department of Radiology, Stanford University, 1201 Welch Road, Stanford, California 94305-5484, USA.

出版信息

Nat Chem. 2010 Jan;2(1):54-60. doi: 10.1038/nchem.480. Epub 2009 Dec 17.

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 either pH, disulfide reduction or enzymatic cleavage. In vitro, the size and shape of the condensation products, and the 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.

摘要

通过受控合成和分子组装,生物系统能够将分子组织成执行复杂过程的超分子结构。尽管化学家已经报道了一些在水中进行超分子组装的例子,但在体内对大分子和结构进行可控的共价合成仍然具有挑战性。在这里,我们报告了在 pH 值、二硫键还原或酶切控制下,1,2-氨硫醇与 2-氰基苯并噻唑之间的缩合反应在体外和活细胞中发生的情况。在体外,缩合产物的大小和形状以及随后组装的纳米结构在每种情况下都不同,因此可以通过调节单体的结构来控制。直接对细胞中获得的产物进行成像,揭示了它们的位置——在酶切控制下靠近高尔基体——证明了在活细胞中进行可控和局部反应的可行性。这种细胞内缩合过程使我们能够对弗林蛋白酶的蛋白水解活性进行成像。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7765/3196337/e8c78fe6d742/nihms159164f1.jpg

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