Supercomplex

However, is supercomplex 27 the true intermediate As previously mentioned, Sugasawa reported that reaction did not proceed with N,N-dialkyl anilines. Do N,N-dialkylanilines form a similar supercomplex We examined the following three anilines, ArNH2, ArNHMe, and ArNMe2, as shown in Figure 1.3. Under Sugasawa conditions at room temperature, formation of the corresponding supercomplex, respectively (29,30, and 31) was confirmed, based on their NMR analyses (Complex 29 and 31 were derived from toluidine and complex 30 comes from aniline). 

Figure 1.3 Structure of the supercomplex from NH2, NHMe, and NMe2 anilines.

It forms supercomplexes consisting of both the ubiquitinating and the proteolytic machineries. According to this model, the substrate first binds to the CSN, is then ubiquitinated by the associated Ub ligase and finally directly charmeled into the 26S proteasome. Deneddylation, deubiquitination and phosphorylation are necessary to maintain the supercomplex, to protect the intermediates and to stimulate proteolysis. 

Such supercomplexes may serve as models for the transition state of crown-assisted reactions, for example nucleophilic substitutions. The observed stereo-specifity could be caused by locally ordered structures in which the crown ether cation complex could act as the substrate and as the anion, as well. 

The expression and characterization of a recombinant subunit II of the archaebacterial terminal oxidase complex in Sulfolobus acidocaldarius was achieved. The binuclear CuA centre was shown to be correctly inserted. A protonation of one of the coordinating histidines was suggested from the pH-profile.109 The subunit is part of a supercomplex SoxM which also has been isolated in a catalytically competent form for the first time.110 Nitrous oxide reductase (NOR) was prepared from Hyphomicrobium denitrificans and charac-... 

Kargul, J., Nield, J., Barber, J. (2003) Three -dimensional reconstruction of a light-harvesting Complex I-Photosystem I (LHCI-PSI) supercomplex from the green alga Chlamydomonas rein-hardtii., J. Biol. Chem. 278, 16,135-16,141. 

The binding of complex anions of transition metals such as the hexacyanides M(CN)6m yields second-coordination-sphere complexes, supercomplexes, [3.13a] and affects markedly their electrochemical [3.21, 3.22] and photochemical [3.23] properties. 

Table 4.3 Binding constants (log K) for the stepwise formation of supercomplexes between 4.14 (n = 3-5) and [Fe(CN)6 4 according to the reactions shown.20...

Bencini, A., Bianchi, A., Garciaespana, E., et al., Anion coordination chemistry. 2. Electrochemical, thermodynamic, and structural studies on supercomplex formation between large polyammonium cycloalkanes and the 2 complex anions hexacyanoferrate(Ii) and hexacyanocobaltate(Iii). Inorg. Chem. 1987, 26, 3902-3907. 

Advantages of Supercomplexes for Electron Transfer There is growing evidence that mitochondrial Complexes I, II, III, and IV are part of a larger supercomplex. What might be the advantage of having all four complexes within a supercomplex ... 

Answer When electron-carrying complexes are bound together in a supercomplex, electron flow between complexes occurs in a solid state this electron movement is kinetically favored compared with the situation in which electron flow depends on each complex diffusing to and colliding with the next complex in the chain. 

Melkozernov AN, Barber J, Blankenship RE. Light harvesting in photosystem I supercomplexes. Biochemistry 2006 45 331-46. 

Figure 9 The bacterial supercomplexes foimd in purple bacteria (Rhodopseudomonas palustris). A single reaction center complex is surrormded by a nearly circular ring of LHl. In close proximity are additional smaller rings of LHII. A gap exists in the LHl ring in some but not necessarily all cases, presumably for the entry of PufX or some other protein...

In cyanobacteria under conditions of iron limitation leading to iron stress, the phycobilosomes are deconstructed, and a macromolecular supercomplex is synthesized. Iron stress induces the expression of a protein that is very similar in structure to CP43, only lacking the large hydrophilic loop that joins the ends of transmembrane helices 5 and 5, and is called C43 CP43 is encoded by the isiA gene. Another... 

Prochloron didemni, is a symbiont that lives in a layer under the body of a marine ascidian. An 18-subunit ring structure is not formed around PSl, but rather a separate macromolecular complex of ten Pcb subunits and two PSll complexes form a supercomplex. As shown in Figure 10(b), two complexes of PSll make up the core of the supercomplex. Five Pcb subunits hue in a row on either side of the core. It is assumed, based upon sequence and structural homology to CP43, that thirteen chlorophylls bind to each Pcb subunit. 

To overcome the lack of sensitization of the lanthanide emissions for the complex of dendrimers 5 (see above), a supra-molecular approach has been pursued (41). It was known that complexes of Ru containing 2,2 -bipyridine (bpy) and cyanide ligands, that is, [Ru(bpy)2(CN)2] and [Ru(bpy)(CN)4] , are liuni-nescent and can play the role of ligands giving rise to supercomplexes (42,43). Titration of an acetonitrileidichloromethane 1 1 (v/v) solution of [Ru(bpy)2(CN)2] with Nd causes... 

Fe (CN)6] , when included in 17, is involved in an electron transfer reaction with iodide which cannot take place in the absence of the macrocyclic species. In fact, the E°(Fe 7Fe ) value for the hexacyano complex is considerably lower than E°(l2/I ), so that the electron transfer from I to Fe center is thermodynamically disfavored. However, in the presence of 17, in an acidic aqueous solution (e.g., pH = 4.4), the redox potential of Fe /Fe couple inside the supercomplex is increased to such an extent that the reaction (see Eq. 1), which is essentially iso-ergonic, proceeds to an equilibrium situation K = 1 M , at 25 °C). 

Flash irradiation with visible light (2 > 400 nm) of a thermally equilibrated solution gives rise to an instantaneous increase of the I3 concentration, followed by a slow decrease in the dark. Although the extremely short lifetime of the [Fe(CN)6] excited state prevents any type of bimolecular process, a photoinduced electron transfer process is responsible for the increased I3 concentration upon irradiation. The positively charged supercomplex forms an ion pair with the iodide anion, so that a very fast electron transfer process can take place following a imimolecular kinetics. 

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