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1.
Nucleic Acids Res ; 51(5): 2011-2032, 2023 03 21.
Artículo en Inglés | MEDLINE | ID: mdl-36617428

RESUMEN

Transfer RNA (tRNA) molecules are essential to decode messenger RNA codons during protein synthesis. All known tRNAs are heavily modified at multiple positions through post-transcriptional addition of chemical groups. Modifications in the tRNA anticodons are directly influencing ribosome decoding and dynamics during translation elongation and are crucial for maintaining proteome integrity. In eukaryotes, wobble uridines are modified by Elongator, a large and highly conserved macromolecular complex. Elongator consists of two subcomplexes, namely Elp123 containing the enzymatically active Elp3 subunit and the associated Elp456 hetero-hexamer. The structure of the fully assembled complex and the function of the Elp456 subcomplex have remained elusive. Here, we show the cryo-electron microscopy structure of yeast Elongator at an overall resolution of 4.3 Å. We validate the obtained structure by complementary mutational analyses in vitro and in vivo. In addition, we determined various structures of the murine Elongator complex, including the fully assembled mouse Elongator complex at 5.9 Å resolution. Our results confirm the structural conservation of Elongator and its intermediates among eukaryotes. Furthermore, we complement our analyses with the biochemical characterization of the assembled human Elongator. Our results provide the molecular basis for the assembly of Elongator and its tRNA modification activity in eukaryotes.


The multi-subunit Elongator complex mediates the addition of a carboxymethyl group to wobble uridines in eukaryotic tRNAs. This tRNA modification is crucial to preserve the integrity of cellular proteomes and to protects us against severe neurodegenerative diseases. Elongator is organized in two distinct modules (i) the larger Elp123 subcomplex that binds and modifies the suitable tRNA substrate and (ii) the smaller Elp456 subcomplex that assists the release of the modified tRNA. The presented cryo-EM structures of Elongator show that the assemblies are very dynamic and undergo conformational rearrangements at consecutive steps of the process. Last but not least, the study provides a detailed reaction scheme and shows that the architecture of Elongator is highly conserved from yeast to mammals.


Asunto(s)
Complejos Multiproteicos , Extensión de la Cadena Peptídica de Translación , Proteínas de Unión al ARN , Saccharomyces cerevisiae , Animales , Humanos , Ratones , Microscopía por Crioelectrón , Histona Acetiltransferasas/metabolismo , Unión Proteica , ARN de Transferencia/metabolismo , Saccharomyces cerevisiae/genética , Saccharomyces cerevisiae/metabolismo , Proteínas de Saccharomyces cerevisiae/metabolismo , Complejos Multiproteicos/química , Complejos Multiproteicos/ultraestructura
2.
Molecules ; 26(12)2021 Jun 10.
Artículo en Inglés | MEDLINE | ID: mdl-34200976

RESUMEN

In this article, the results of computational structural studies on Al-containing zeolites, via periodic DFT + D modelling and FDM (Finite Difference Method) to solve the Schrödinger equation (FDMNES) for XAS simulations, corroborated by EXAFS (Extended X-ray Absorption Fine Structure) spectroscopy and PXRD (powder X-ray diffractometry), are presented. The applicability of Radial Distribution Function (RDF) to screen out the postulated zeolite structure is also discussed. The structural conclusions are further verified by HR-TEM imaging.

3.
Nat Commun ; 15(1): 4094, 2024 May 15.
Artículo en Inglés | MEDLINE | ID: mdl-38750017

RESUMEN

tRNA modifications affect ribosomal elongation speed and co-translational folding dynamics. The Elongator complex is responsible for introducing 5-carboxymethyl at wobble uridine bases (cm5U34) in eukaryotic tRNAs. However, the structure and function of human Elongator remain poorly understood. In this study, we present a series of cryo-EM structures of human ELP123 in complex with tRNA and cofactors at four different stages of the reaction. The structures at resolutions of up to 2.9 Å together with complementary functional analyses reveal the molecular mechanism of the modification reaction. Our results show that tRNA binding exposes a universally conserved uridine at position 33 (U33), which triggers acetyl-CoA hydrolysis. We identify a series of conserved residues that are crucial for the radical-based acetylation of U34 and profile the molecular effects of patient-derived mutations. Together, we provide the high-resolution view of human Elongator and reveal its detailed mechanism of action.


Asunto(s)
Microscopía por Crioelectrón , ARN de Transferencia , Humanos , ARN de Transferencia/metabolismo , ARN de Transferencia/química , ARN de Transferencia/genética , Uridina/química , Uridina/metabolismo , Mutación , Acetilcoenzima A/metabolismo , Acetilcoenzima A/química , Modelos Moleculares , Acetilación , Histona Acetiltransferasas/metabolismo , Histona Acetiltransferasas/química , Histona Acetiltransferasas/genética , Unión Proteica
4.
Sci Adv ; 9(2): eadd9688, 2023 01 13.
Artículo en Inglés | MEDLINE | ID: mdl-36638176

RESUMEN

Plants use solar energy to power cellular metabolism. The oxidation of plastoquinol and reduction of plastocyanin by cytochrome b6f (Cyt b6f) is known as one of the key steps of photosynthesis, but the catalytic mechanism in the plastoquinone oxidation site (Qp) remains elusive. Here, we describe two high-resolution cryo-EM structures of the spinach Cyt b6f homodimer with endogenous plastoquinones and in complex with plastocyanin. Three plastoquinones are visible and line up one after another head to tail near Qp in both monomers, indicating the existence of a channel in each monomer. Therefore, quinones appear to flow through Cyt b6f in one direction, transiently exposing the redox-active ring of quinone during catalysis. Our work proposes an unprecedented one-way traffic model that explains efficient quinol oxidation during photosynthesis and respiration.


Asunto(s)
Citocromos b , Plastocianina , Citocromos b/metabolismo , Plastocianina/metabolismo , Microscopía por Crioelectrón , Complejo de Citocromo b6f/química , Complejo de Citocromo b6f/metabolismo , Oxidación-Reducción , Fotosíntesis , Plantas/metabolismo , Quinonas , Transporte de Electrón
5.
Nanoscale ; 14(8): 3224-3233, 2022 Feb 24.
Artículo en Inglés | MEDLINE | ID: mdl-35156989

RESUMEN

The increasing interest in virus-like particles (VLPs) has been reflected by the growing number of studies on their assembly and application. However, the formation of complete VLPs is a complex phenomenon, making it difficult to rationally design VLPs with desired features de novo. In this paper, we describe VLPs assembled in vitro from the recombinant capsid protein of brome mosaic virus (BMV). The analysis of VLPs was performed by Cryo-EM reconstructions and allowed us to visualize a few classes of VLPs, giving insight into the VLP self-assembly process. Apart from the mature icosahedral VLP practically identical with native virions, we describe putative VLP intermediates displaying non-icosahedral arrangements of capsomers, proposed to occur before the final disorder-order transition stage of icosahedral VLP assembly. Some of the described VLP classes show a lack of protein shell continuity, possibly resulting from too strong interaction with the cargo (in this case tRNA) with the capsid protein. We believe that our results are a useful prerequisite for the rational design of VLPs in the future and lead the way to the effective production of modified VLPs.


Asunto(s)
Bromovirus , Cápside/química , Proteínas de la Cápside/química , Microscopía por Crioelectrón , Virión/química , Ensamble de Virus
6.
EMBO Mol Med ; 14(7): e15608, 2022 07 07.
Artículo en Inglés | MEDLINE | ID: mdl-35698786

RESUMEN

The highly conserved Elongator complex is a translational regulator that plays a critical role in neurodevelopment, neurological diseases, and brain tumors. Numerous clinically relevant variants have been reported in the catalytic Elp123 subcomplex, while no missense mutations in the accessory subcomplex Elp456 have been described. Here, we identify ELP4 and ELP6 variants in patients with developmental delay, epilepsy, intellectual disability, and motor dysfunction. We determine the structures of human and murine Elp456 subcomplexes and locate the mutated residues. We show that patient-derived mutations in Elp456 affect the tRNA modification activity of Elongator in vitro as well as in human and murine cells. Modeling the pathogenic variants in mice recapitulates the clinical features of the patients and reveals neuropathology that differs from the one caused by previously characterized Elp123 mutations. Our study demonstrates a direct correlation between Elp4 and Elp6 mutations, reduced Elongator activity, and neurological defects. Foremost, our data indicate previously unrecognized differences of the Elp123 and Elp456 subcomplexes for individual tRNA species, in different cell types and in different key steps during the neurodevelopment of higher organisms.


Asunto(s)
ARN de Transferencia , Proteínas de Saccharomyces cerevisiae , Animales , Ratones , Subunidades de Proteína/química , Subunidades de Proteína/genética , Subunidades de Proteína/metabolismo , ARN de Transferencia/química , ARN de Transferencia/genética , ARN de Transferencia/metabolismo , Proteínas de Saccharomyces cerevisiae/química , Proteínas de Saccharomyces cerevisiae/metabolismo
7.
Materials (Basel) ; 14(16)2021 Aug 11.
Artículo en Inglés | MEDLINE | ID: mdl-34443036

RESUMEN

In our study, the comparison of the automatically detected precipitates in L-PBF Inconel 625, with experimentally detected phases and with the results of the thermodynamic modeling was used to test their compliance. The combination of the complementary electron microscopy techniques with the microanalysis of chemical composition allowed us to examine the structure and chemical composition of related features. The possibility of automatic detection and identification of precipitated phases based on the STEM-EDS data was presented and discussed. The automatic segmentation of images and identifying of distinguishing regions are based on the processing of STEM-EDS data as multispectral images. Image processing methods and statistical tools are applied to maximize an information gain from data with low signal-to-noise ratio, keeping human interactions on a minimal level. The proposed algorithm allowed for automatic detection of precipitates and identification of interesting regions in the Inconel 625, while significantly reducing the processing time with acceptable quality of results.

8.
Nanoscale ; 11(1): 89-97, 2018 Dec 20.
Artículo en Inglés | MEDLINE | ID: mdl-30226243

RESUMEN

Reduced titanium oxide structures are regarded as promising materials for various catalytic and optoelectronic applications. There is thus an urgent need for developing methods of controllable formation of crystalline nanostructures with tunable oxygen nonstoichiometry. We introduce the Extremely Low Oxygen Partial Pressure (ELOP) method, employing an oxygen getter in close vicinity to an oxide during thermal reduction under vacuum, as an effective bottom-up method for the production of nanowires arranged in a nanoscale metallic network on a SrTiO3 perovskite surface. We demonstrate that the TiO nanowires crystallize in a highly ordered cubic phase, where single nanowires are aligned along the main crystallographic directions of the SrTiO3 substrate. The dimensions of the nanostructures are easily tunable from single nanometers up to the mesoscopic range by varying the temperature of reduction. The interface between TiO and SrTiO3 (metal and insulator) was found to be atomically sharp providing the unique possibility of the investigation of electronic states, especially since the high conductivity of the TiO nanostructures is maintained after room temperature oxidation. According to the growth model we propose, TiO nanowire formation is possible due to the incongruent sublimation of strontium and crystallographic shearing, triggered by the extremely low oxygen partial pressure (ELOP). The controlled formation of conductive nanowires on a perovskite surface holds technological potential for implementation in memristive devices, organic electronics, or for catalytic applications, and provides insight into the mechanism of nanoscale phase transformations in metal oxides. We believe that the ELOP mechanism of suboxide formation is suitable for the formation of reduced suboxides on other perovskite oxides and for the broader class of transition metal oxides.

9.
Beilstein J Nanotechnol ; 5: 1463-71, 2014.
Artículo en Inglés | MEDLINE | ID: mdl-25247129

RESUMEN

By using scanning tunnelling potentiometry we characterized the lateral variation of the electrochemical potential µec on the gold-induced Ge(001)-c(8 × 2)-Au surface reconstruction while a lateral current flows through the sample. On the reconstruction and across domain boundaries we find that µec shows a constant gradient as a function of the position between the contacts. In addition, nanoscale Au clusters on the surface do not show an electronic coupling to the gold-induced surface reconstruction. In combination with high resolution scanning electron microscopy and transmission electron microscopy, we conclude that an additional transport channel buried about 2 nm underneath the surface represents a major transport channel for electrons.

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