Academic literature on the topic 'SnAP-reagents'

Saturated nitrogen heterocycles can be found with increasing abundance in bioactive molecules despite a limited number of methods to access these scaffolds. However, the coupling of recently introduced SnAP [tin (Sn) amine protocol] reagents with a wide range of aldehydes and ketones has proven to be a reliable, practical, and versatile one-step approach to saturated N-heterocycles. While effective, the lack of mechanistic understanding limits efforts to develop new catalytic and enantioselective variants. To distinguish between a polar or radical mechanism, we assessed Lewis and Brønsted acids, radical trapping experiments, and radical clock SnAP reagents reinforcing the current understanding of the SnAP protocol as a radical cyclization.

We report the first set of selenium-containing SnAP reagents for the direct synthesis of C-substituted selenomorpholines and 1,4-selenazepanes and the biological evaluation of these elusive N-heterocycles.

Antibodies are indispensable reagents in basic research, and those raised against tags constitute a useful tool for the evaluation of the biochemistry and biology of novel proteins. In this paper, we describe the isolation and characterization of a single-domain recombinant antibody (VHH) specific for the SNAP-tag, using Twist2 as a test-protein. The antibody was efficient in western blot, immunoprecipitation, immunopurification, and immunofluorescence. The sequence corresponding to the anti-SNAP has been subcloned for large-scale expression in vectors that allow its fusion to either a 6xHis-tag or the Fc domain of rabbit IgG2 taking advantage of a new plasmid that was specifically designed for VHH antibodies. The two different fusion antibodies were compared in immunopurification and immunofluorescence experiments, and the recombinant protein SNAP-Twist2 was accurately identified by the anti-SNAP Fc-VHH construct in the nuclear/nucleolar subcellular compartment. Furthermore, such localization was confirmed by direct Twist2 identification by means of anti-Twisit2 VHH antibodies recovered after panning of the same naïve phage display library used to isolate the anti-SNAP binders. Our successful localization of Twist2 protein using the SNAP-tag-based approach and the anti-Twist2-specific recombinant single-domain antibodies opens new research possibilities in this field.

2017 - 2018
In the last few years, computational chemistry has played an important role in disclosing novel compounds with relevant biological activity. Inflammation and cancer processes have been recently linked, and the identification of new molecular entities able to interfere with biological targets involved in these pathologies is strongly needed. The analysis of ligand-macromolecule interactions and the evaluation of possible “binding modes” are the starting points in the design and the identification of new and more powerful drugs. Also, in silico Virtual Screening campaigns of large libraries of compounds on a specific target allow the selection of the most promising, leading the identification of new hits. Moreover, the coupling between versatile synthetic approaches and computational protocols is a powerful tool to obtain optimal results with time optimization. Thus, in this thesis both topics are applied at the same time, as they are connected to each other. The research work was mainly focused on mPGES-1 (microsomal Prostaglandin E2 Synthase) as a promising target for the treatment of the pathologies above. This enzyme is a homotrimeric membrane protein involved in the arachidonic acid cascade and it acts as downstream synthase in the cyclooxygenase pathway, catalyzing the conversion of the unstable peroxidic intermediate prostaglandin H2 (PGH2) in prostaglandin E2 (PGE2). Among the three different isoforms of the enzyme, selective inhibition of the inducible mPGES-1 may be considered a valid therapeutic approach to interfere with inflammation-induced PGE2 formation, avoiding to block the biosynthesis of constitutive prostanoids. Also, it is over-expressed in tumor pathologies. In light of this, in order to identify novel molecular platforms able to inhibit the activity of the enzyme strongly, a structure-based multi-step computational protocol was applied starting from selected privileged scaffolds coupled to a synthetic chemical route. Specifically, new libraries of 2-aminobenzothiazole, 2-aminothiadiazole and 2-carboxamidepyrrole-based molecules were generated, and they were docked onto the 3D structure of mPGES-1 (PDB code: 4BPM) crystallized in 2014. Using the interactions with the receptor counterpart as a qualitative filter, a collection of compounds for each library was selected, synthesized and submitted to biological investigation. Finally, cell-free and cell line assays confirmed some of them (benzothiazole derivatives 1, 3, 6, 9 and 13, thiadiazole derivatives 18-20 and 22, pyrrole derivatives 45 and 47) as novel promising mPGES-1 inhibitors. Furthermore, the same computational approach focused on mPGES-1 was applied on substituted saturated N-heterocycles, whose synthesis was performed at the Department of Chemistry and Applied Biosciences at ETH (Zurich). In detail, the libraries were docked onto the crystal structure co-crystallized with the inhibitor 6PW (PDB code: 5K0I), leading to the selection of 21 compounds (62-82). The synthesis was performed using the SnAP (Stannyl Amine Protocol) chemistry, which consists of a reaction between an aminotributylstannane and an aldehyde to form an imine as the first step, followed by an intramolecular cyclization. Biological investigations are in progress on the synthesized compounds. In order to deeply combine computational tools and this versatile and suitable synthetic approach, a large database of about 1,300,000 synthetically accessible compounds was created in silico starting from iSnAP (Iterative SnAP) reagents, a new generation of SnAP reagents bearing a further functional group. The prepared database was then submitted to virtual screening studies on pharmacologically promising targets (mPGES-1 up to now), in order to select the best candidates for the synthesis and the biological evaluation. Finally, the application of multi-step computational protocols including both ligand and structure based approaches took place in the identification of two novel 3-hydroxy-3-pyrrolin-2-one-based hits (compounds 87 and 88) as promising mPGES-1 inhibitors, starting from a large library of commercially available compounds. A second research work regarded Hsp90, a molecular chaperone involved in the development, survival and proliferation of cancer cells, regulating the homeostasis of oncoproteins. Most of the developed Hsp90 inhibitors interact with the N-terminal domain, but this type of modulation induces toxicity issues connected to the induction of the deleterious heat shock response (HSR). Contrariwise, since C-terminus inhibitors do not produce this effect and only a few of them have been developed so far, an aim of this research work consisted of the individuation of novel C-terminus binders. Thus, a biological screening on a small library of 48 commercially available compounds was performed and two novel inhibitors were identified (compounds 100 and 103) able to interact selectively with the C-terminal domain. Starting from these results, a computational rationalization was performed, applying Induced Fit Docking studies and Molecular Dynamic Simulations. In conclusion, in order to perform an optimization campaign, three large libraries of derivatives of compound 103 were generated using the multi-step computational protocol above, and a total number of 21 molecules have been selected for the synthesis and the biological evaluation. [edited by Author]
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