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Andrew D. Ellington

Researcher at University of Texas at Austin

Publications -  599
Citations -  48723

Andrew D. Ellington is an academic researcher from University of Texas at Austin. The author has contributed to research in topics: Aptamer & RNA. The author has an hindex of 96, co-authored 569 publications receiving 43262 citations. Previous affiliations of Andrew D. Ellington include Harvard University & UPRRP College of Natural Sciences.

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Analysis of DNA-guided self-assembly of microspheres using imaging flow cytometry.

TL;DR: The analysis demonstrated that self-assembly of 50 bp microspheres can be driven nearly to completion by stoichiometric excess in a manner similar to Le Chatelier's principle in common chemical equilibrium.
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Analyzing machupo virus-receptor binding by molecular dynamics simulations.

TL;DR: In this paper, the machupo virus (MACV) spike glycoprotein (GP1) was removed from the human transferrin receptor (hTfR1) using the maximum applied force of separation and the area under the force-versus-distance curve.
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A docking and modelling strategy for peptide–RNA complexes: applications to BIV Tat–TAR and HIV Rev–RBE

TL;DR: A general strategy for docking and modelling RNA-protein complexes has been developed and the resulting model of the Rev34-50-RBE complex predicts that although no single arginine sidechain is responsible for complex formation, residues Arg2, Arg5 and Arg11 are more important for binding than the otherArginine residues in the peptide.
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Characteristics of amino acids.

TL;DR: This appendix presents useful basic information, including common abbreviations, useful measurements and data, characteristics of amino acids and nucleic acids, information on radioactivity and the safe use of radioisotopes and other hazardous chemicals, conversions for centrifuges and rotors, characteristics for common detergents, and common conversion factors.
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Expanded Genetic Codes Create New Mutational Routes to Rifampicin Resistance in Escherichia coli

TL;DR: This work explored how Escherichia coli strains that incorporate a 21st nonstandard amino acid at the recoded amber (TAG) stop codon evolve resistance to the antibiotic rifampicin and found that a variety of mutations that lead to substitutions of nsAAs in the essential RpoB protein confer robust rifampsicin resistance.