Literature DB >> 19334012

An intrinsically fluorescent recognition ligand scaffold based on chaperonin protein and semiconductor quantum-dot conjugates.

Hongzhi Xie1, Yi-Fen Li, Hiromi K Kagawa, Jonathan D Trent, Kumara Mudalige, Mircea Cotlet, Basil I Swanson.   

Abstract

Genetic engineering of a novel protein-nanoparticle hybrid system with great potential for biosensing applications and for patterning of various types of nanoparticles is described. The hybrid system is based on a genetically modified chaperonin protein from the hyperthermophilic archaeon Sulfolobus shibatae. This chaperonin is an 18-subunit double ring, which self-assembles in the presence of Mg ions and ATP. Described here is a mutant chaperonin (His-beta-loopless, HBLL) with increased access to the central cavity and His-tags on each subunit extending into the central cavity. This mutant binds water-soluble semiconductor quantum dots, creating a protein-encapsulated fluorescent nanoparticle. The new bioconjugate has high affinity, in the order of strong antibody-antigen interactions, a one-to-one protein-nanoparticle stoichiometry, and high stability. By adding selective binding sites to the solvent-exposed regions of the chaperonin, this protein-nanoparticle bioconjugate becomes a sensor for specific targets.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19334012     DOI: 10.1002/smll.200801106

Source DB:  PubMed          Journal:  Small        ISSN: 1613-6810            Impact factor:   13.281


  1 in total

1.  Specific Internalisation of Gold Nanoparticles into Engineered Porous Protein Cages via Affinity Binding.

Authors:  David Paramelle; Tao Peng; Paul Free; David G Fernig; Sierin Lim; Nikodem Tomczak
Journal:  PLoS One       Date:  2016-09-13       Impact factor: 3.240

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.