Chapter 15: Light-activated Bioconjugate Complexes
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Published:07 Dec 2011
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Special Collection: 2011 ebook collection , 2011 ebook collection , ECCC Environmental eBooks 1968-2022 , 2011-2015 environmental chemistry subject collectionSeries: Energy and Environment
D. Hvasanov, D. C. Goldstein, and P. Thordarson, in Molecular Solar Fuels, ed. T. J. Wydrzynski and W. Hillier, The Royal Society of Chemistry, 2011, ch. 15, pp. 426-447.
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This Chapter describes the various methods that are available for linking synthetic and biological light-activated or light-harvesting units to electron acceptors. The bioconjugate approaches discussed are divided into classical and non-classical approaches. The classical methods include modification of amine (lysine and α-N-terminus), cysteine, histidine, tyrosine and glutamine residues of the target proteins. Non-classical approaches discussed include recombinant methods for introducing non-natural amino acids, ‘click’ chemistry, carbonyl condensation and Michael addition reactions. Emphasis will be on examples from the literature that describe the bioconjugation of synthetic light-activated chromophores to redox proteins. The Chapter concludes with a few recent examples from the literature on light-activated chromophore-electron acceptor bioconjugates, including cytochrome complexes modified with Ru-organometallic complexes and Photosystem I modified with metallic nanoparticle electron acceptors.