8DYK
Room temperature neutron structure of a fluorescent Ag8 cluster templated by a multistranded DNA scaffold
8DYK の概要
エントリーDOI | 10.2210/pdb8dyk/pdb |
関連するPDBエントリー | 6NIZ |
分子名称 | DNA (5'-D(*AP*AP*CP*CP*CP*C)-3'), SILVER ION (3 entities in total) |
機能のキーワード | dna, metal clusters, silver, chromophore |
由来する生物種 | synthetic construct |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 4662.91 |
構造登録者 | |
主引用文献 | David, F.,Setzler, C.,Sorescu, A.,Lieberman, R.L.,Meilleur, F.,Petty, J.T. Mapping H + in the Nanoscale (A 2 C 4 ) 2 -Ag 8 Fluorophore. J Phys Chem Lett, 13:11317-11322, 2022 Cited by PubMed Abstract: When strands of DNA encapsulate silver clusters, supramolecular optical chromophores develop. However, how a particular structure endows a specific spectrum remains poorly understood. Here, we used neutron diffraction to map protonation in (AC)-Ag, a green-emitting fluorophore with a "Big Dipper" arrangement of silvers. The DNA host has two substructures with distinct protonation patterns. Three cytosines from each strand collectively chelate handle-like array of three silvers, and calorimetry studies suggest Ag cross-links. The twisted cytosines are further joined by hydrogen bonds from fully protonated amines. The adenines and their neighboring cytosine from each strand anchor a dipper-like group of five silvers via their deprotonated endo- and exocyclic nitrogens. Typically, exocyclic amines are strongly basic, so their acidification and deprotonation in (AC)-Ag suggest that silvers perturb the electron distribution in the aromatic nucleobases. The different protonation states in (AC)-Ag suggest that atomic level structures can pinpoint how to control and tune the electronic spectra of these nanoscale chromophores. PubMed: 36453924DOI: 10.1021/acs.jpclett.2c03161 主引用文献が同じPDBエントリー |
実験手法 | NEUTRON DIFFRACTION (2.1 Å) |
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