scholarly journals Nano-sandwich composite by kinetic trapping assembly from protein and nucleic acid

2021 ◽  
Vol 49 (17) ◽  
pp. 10098-10105
Author(s):  
Shi Chen ◽  
Li Xing ◽  
Douglas Zhang ◽  
Alba Monferrer ◽  
Thomas Hermann

Abstract Design and preparation of layered composite materials alternating between nucleic acids and proteins has been elusive due to limitations in occurrence and geometry of interaction sites in natural biomolecules. We report the design and kinetically controlled stepwise synthesis of a nano-sandwich composite by programmed noncovalent association of protein, DNA and RNA modules. A homo-tetramer protein core was introduced to control the self-assembly and precise positioning of two RNA–DNA hybrid nanotriangles in a co-parallel sandwich arrangement. Kinetically favored self-assembly of the circularly closed nanostructures at the protein was driven by the intrinsic fast folding ability of RNA corner modules which were added to precursor complex of DNA bound to the protein. The 3D architecture of this first synthetic protein–RNA–DNA complex was confirmed by fluorescence labeling and cryo-electron microscopy studies. The synthesis strategy for the nano-sandwich composite provides a general blueprint for controlled noncovalent assembly of complex supramolecular architectures from protein, DNA and RNA components, which expand the design repertoire for bottom-up preparation of layered biomaterials.

2019 ◽  
Vol 23 (11n12) ◽  
pp. 1308-1325 ◽  
Author(s):  
Elena Prigorchenko ◽  
Lukas Ustrnul ◽  
Victor Borovkov ◽  
Riina Aav

Porphyrins are prominent host molecules which are widely used due to their structural characteristics and directional interaction sites. This review summarizes non-covalently bound ternary complexes of porphyrins, constructed from at least three non-identical species. Progress in supramolecular chemistry allows the creation of complex molecular machinery tools, such as rotors, motors and switches from relatively simple structures in a single self-assembly step. In the current review, we highlight the collection of sophisticated molecular ensembles including sandwich-type complexes, cages, capsules, tweezers, rotaxanes, and supramolecular architectures mediating oxygen-binding and oxidation reactions. These diverse structures have high potential to be applied in sensing, production of new smart materials as well as in medical science.


2009 ◽  
Vol 131 (42) ◽  
pp. 15122-15123 ◽  
Author(s):  
Sampath Srinivasan ◽  
Palathingal A. Babu ◽  
Sankarapillai Mahesh ◽  
Ayyappanpillai Ajayaghosh

2008 ◽  
Vol 879 (1-3) ◽  
pp. 1-6 ◽  
Author(s):  
R. Prajapati ◽  
L. Mishra ◽  
S.J. Grabowski ◽  
G. Govil ◽  
S.K. Dubey

2006 ◽  
Vol 35 (10) ◽  
pp. 1198-1199 ◽  
Author(s):  
Takayuki Chujo ◽  
Yu Gonda ◽  
Yasunori Oumi ◽  
Tsuneji Sano ◽  
Hideaki Yoshitake

ChemPhysChem ◽  
2020 ◽  
Vol 21 (10) ◽  
pp. 1044-1051 ◽  
Author(s):  
Diego Carnevale ◽  
Marcel Hollenstein ◽  
Geoffrey Bodenhausen

Molecules ◽  
2020 ◽  
Vol 25 (7) ◽  
pp. 1733 ◽  
Author(s):  
Ana Miljkovic ◽  
Sonia La Cognata ◽  
Greta Bergamaschi ◽  
Mauro Freccero ◽  
Antonio Poggi ◽  
...  

In this work, we report the synthesis of a new bis(tris(2-aminoethyl)amine) azacryptand L with triphenyl spacers. The binding properties of its dicopper complex for aromatic dicarboxylate anions (as TBA salts) were investigated, with the aim to obtain potential building blocks for supramolecular structures like rotaxanes and pseudo-rotaxanes. As expected, UV-Vis and emission studies of [Cu2L]4+ in water/acetonitrile mixture (pH = 7) showed a high affinity for biphenyl-4,4′-dicarboxylate (dfc2−), with a binding constant of 5.46 log units, due to the best match of the anion bite with the Cu(II)-Cu(II) distance in the cage’s cavity. Compared to other similar bistren cages, the difference of the affinity of [Cu2L]4+ for the tested anions was not so pronounced: conformational changes of L seem to promote a good interaction with both long (e.g., dfc2−) and short anions (e.g., terephthalate). The good affinity of [Cu2L]4+ for these dicarboxylates, together with hydrophobic interactions within the cage’s cavity, may promote the self-assembly of a stable 1:1 complex in water mixture. These results represent a good starting point for the application of these molecular systems as building units for the design of new supramolecular architectures based on non-covalent interactions, which could be of interest in all fields related to supramolecular devices.


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