The accomplices: Heparan sulfates and N-glycans foster SARS-CoV-2 spike:ACE2 receptor binding and virus priming DOI Creative Commons
Giulia Paiardi, Matheus Ferraz, Marco Rusnati

и другие.

bioRxiv (Cold Spring Harbor Laboratory), Год журнала: 2024, Номер unknown

Опубликована: Фев. 5, 2024

Abstract Although it is well established that the SARS-CoV-2 spike glycoprotein binds to host cell ACE2 receptor initiate infection, far less known about tissue tropism and susceptibility virus. Differential expression across different types of heparan sulfate (HS) proteoglycans, with variably sulfated glycosaminoglycans (GAGs), their synergistic interactions viral N-glycans may contribute susceptibility. Nevertheless, contribution remains unclear since HS evade experimental characterization. We, therefore, carried out microsecond-long all-atom molecular dynamics simulations, followed by random acceleration fully glycosylated spike:ACE2 complex without highly GAG chains bound. By considering model GAGs as surrogates for expressed in lung cells, we identified key novel entry mechanisms SARS-CoV-2. We find promotes structural energetic stabilization active conformation binding domain (RBD) reorientation toward N-terminal same subunit RBD. Spike exert effects, promoting better packing, strengthening protein:protein interaction, prolonging residence time complex. trigger rearrangement S2’ functional protease cleavage site through allosteric interdomain communication. These results thus show has a multifaceted role facilitating infection they provide mechanistic basis development derivatives anti-SARS-CoV-2 potential. Significance Statement A blocking understand why infects some more than others. Heparan proteoglycans are differentially on surface cells and, receptors, an route Here, used computer simulations investigate how glycosaminoglycans, lungs, impact interaction between virus ACE2. The indicate HS, together N-glycans, stabilizes triggers changes, including cleavage, contributing mechanism. This study lays understanding cell-specificity developing strategies inhibiting infection.

Язык: Английский

Role of N343 glycosylation on the SARS-CoV-2 S RBD structure and co-receptor binding across variants of concern DOI Creative Commons
Callum M. Ives, Linh Nguyen, Carl A. Fogarty

и другие.

eLife, Год журнала: 2024, Номер 13

Опубликована: Март 27, 2024

Glycosylation of the SARS-CoV-2 spike (S) protein represents a key target for viral evolution because it affects both evasion and fitness. Successful variations in glycan shield are difficult to achieve though, as glycosylation is also critical folding structural stability. Within this framework, identification sites that structurally dispensable can provide insight into evolutionary mechanisms inform immune surveillance. In work, we show through over 45 μs cumulative sampling from conventional enhanced molecular dynamics (MD) simulations, how structure immunodominant S receptor binding domain (RBD) regulated by N -glycosylation at N343 glycan’s role changes WHu-1, alpha (B.1.1.7), beta (B.1.351), delta (B.1.617.2), omicron (BA.1 BA.2.86) variants. More specifically, find amphipathic nature -glycan instrumental preserve integrity RBD hydrophobic core loss triggers specific consistent conformational change. We change allosterically regulates conformation motif (RBM) alpha, RBDs, but not variants, due mutations reinforce architecture. support these findings, monosialylated ganglioside co-receptors highly dependent on RBD, affinity significantly across VoCs. Ultimately, functional work reinforces our understanding function allows us identify constraints within which site become hotspot shield.

Язык: Английский

Процитировано

4

The accomplices: Heparan sulfates and N-glycans foster SARS-CoV-2 spike:ACE2 receptor binding and virus priming DOI Creative Commons
Giulia Paiardi, Matheus Ferraz, Marco Rusnati

и другие.

Proceedings of the National Academy of Sciences, Год журнала: 2024, Номер 121(43)

Опубликована: Окт. 14, 2024

Although it is well established that the SARS-CoV-2 spike glycoprotein binds to host cell ACE2 receptor initiate infection, far less known about tissue tropism and susceptibility virus. Differential expression across different types of heparan sulfate (HS) proteoglycans, with variably sulfated glycosaminoglycans (GAGs), their synergistic interactions viral N-glycans may contribute susceptibility. Nevertheless, contribution remains unclear since HS evade experimental characterization. We, therefore, carried out microsecond-long all-atom molecular dynamics simulations, followed by random acceleration fully glycosylated spike:ACE2 complex without highly GAG chains bound. By considering model GAGs as surrogates for expressed in lung cells, we identified key entry mechanisms SARS-CoV-2. We find promotes structural energetic stabilization active conformation receptor-binding domain (RBD) reorientation toward N-terminal same subunit RBD. Spike exert effects, promoting better packing, strengthening protein:protein interaction, prolonging residence time complex. binding trigger rearrangement S2’ functional protease cleavage site through allosteric interdomain communication. These results thus show has a multifaceted role facilitating they provide mechanistic basis development derivatives anti-SARS-CoV-2 potential.

Язык: Английский

Процитировано

4

Many Roles of Carbohydrates: A Computational Spotlight on the Coronavirus S Protein Binding DOI Creative Commons
Suman Maity, Atanu Acharya

ACS Applied Bio Materials, Год журнала: 2023, Номер 7(2), С. 646 - 656

Опубликована: Март 22, 2023

Glycosylation is one of the post-translational modifications with more than 50% human proteins being glycosylated. The exact nature and chemical composition glycans are inaccessible to X-ray or cryo-electron microscopy imaging techniques. Therefore, computational modeling studies molecular dynamics must be used as a "computational microscope". spike (S) protein SARS-CoV-2 heavily glycosylated, few play functional role "beyond shielding". In this mini-review, we discuss investigations roles specific S-protein ACE2 in overall ACE2-S binding. We highlight different functions demonstrated myriad models simulations context virus binding receptor. also interactions between glycocalyx S protein, which may utilized design prophylactic polysaccharide-based therapeutics targeting protein. addition, underline recent emergence coronavirus variants their impact on its glycans.

Язык: Английский

Процитировано

9

Can ChatGPT pass Glycobiology? DOI

Devin Ormsby Williams,

Elisa Fadda

Glycobiology, Год журнала: 2023, Номер 33(8), С. 606 - 614

Опубликована: Авг. 1, 2023

The release of text-generating applications based on interactive Large Language Models (LLMs) in late 2022 triggered an unprecedented and ever-growing interest worldwide. almost instantaneous success LLMs stimulated lively discussions public media academic fora alike not only the value potentials such tools all areas knowledge information acquisition distribution but also dangers posed by their uncontrolled indiscriminate use. This conversation is now particularly active higher education sector, where are seen as a potential threat to integrity at levels, from facilitating cheating students assignments plagiarizing writing case researchers administrators. Within this framework, we interested testing boundaries LLM ChatGPT (www.openai.com) our scientific expertise analyzing results different perspectives, i.e. final year BSc student, research scientist, lecturer education. To end, paper, present discuss systematic evaluation how addresses progressively complex tasks exam-type questions Carbohydrate Chemistry Glycobiology. project allowed us gain insight on: (i) strengths limitations model provide relevant (most importantly) correct information, (ii) format(s) complexity query required obtain desired output, (iii) strategies integrate teaching learning.

Язык: Английский

Процитировано

9

SARS-CoV-2 spike protein in infectivity DOI
Alaa Muayad Altaie, Rania Hamdy,

Mohamed I. Husseiny

и другие.

Elsevier eBooks, Год журнала: 2025, Номер unknown, С. 21 - 56

Опубликована: Янв. 1, 2025

Язык: Английский

Процитировано

0

Subtle Changes at the RBD/hACE2 Interface During SARS-CoV-2 Variant Evolution: A Molecular Dynamics Study DOI Creative Commons
Aria Gheeraert, Vincent Leroux, Dominique Mias‐Lucquin

и другие.

Biomolecules, Год журнала: 2025, Номер 15(4), С. 541 - 541

Опубликована: Апрель 7, 2025

The SARS-CoV-2 Omicron variants show different behavior compared to the previous variants, especially with respect Delta variant, which promotes a lower morbidity despite being much more contagious. In this perspective, we performed molecular dynamics (MD) simulations of spike RBD/hACE2 complexes corresponding WT, and four variants. Carrying out comprehensive analysis residue interactions within between two partners allowed us draw profile each variant by using complementary methods (PairInt, hydrophobic potential, contact PCA). PairInt calculations highlighted residues most involved in electrostatic interactions, make strong contribution binding highly stable RBD hACE2. Apolar contacts made substantial detection patches. Contact networks cross-correlation matrices were able detect subtle changes at point mutations as S375F mutation occurring all is likely confer an advantage stability. This study brings new highlights on dynamic hACE2, may explain final persistence over Delta.

Язык: Английский

Процитировано

0

Mechanisms of allostery at the viral surface through the eyes of molecular simulation DOI Creative Commons
Firdaus Samsudin, Lorena Zuzic, Jan K. Marzinek

и другие.

Current Opinion in Structural Biology, Год журнала: 2023, Номер 84, С. 102761 - 102761

Опубликована: Дек. 23, 2023

Язык: Английский

Процитировано

8

The role ofN-glycosylation in spike antigenicity for the SARS-CoV-2 Gamma variant DOI Open Access
Cassandra L. Pegg, Naphak Modhiran, Rhys Parry

и другие.

bioRxiv (Cold Spring Harbor Laboratory), Год журнала: 2023, Номер unknown

Опубликована: Апрель 7, 2023

Abstract The emergence of SARS-CoV-2 variants alters the efficacy existing immunity towards viral spike protein, whether acquired from infection or vaccination. Mutations that impact N -glycosylation may be particularly important in influencing antigenicity, but their consequences are difficult to predict. Here, we compare glycosylation profiles and antigenicity recombinant ancestral Wu-1 Gamma strain, which has two additional sites due amino acid substitutions N-terminal domain (NTD). We found a mutation at residue 20 threonine asparagine within NTD caused loss NTD-specific antibody binding. Glycan site-occupancy analyses revealed resulted switching new sequon N20 native N17 site. Site-specific demonstrated distinct glycoform differences between Wu-1, Gamma, selected variant proteins, these did not affect Finally, evaluated specificity proteins against convalescent COVID-19 sera reduced cross-reactivity some mutants, compared Wuhan spike. Our results illustrate divergence on binding profiles.

Язык: Английский

Процитировано

6

Stabilization of the Metastable Pre-Fusion Conformation of the SARS-CoV-2 Spike Glycoprotein through N-Linked Glycosylation of the S2 Subunit DOI Creative Commons

Fuwen Zan,

Yao Zhou, Ting Chen

и другие.

Viruses, Год журнала: 2024, Номер 16(2), С. 223 - 223

Опубликована: Янв. 31, 2024

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the novel responsible for disease 2019 (COVID-19) pandemic, represents a serious threat to public health. The spike (S) glycoprotein of SARS-CoV-2 mediates viral entry into host cells and is heavily glycosylated. In this study, we systemically analyzed roles 22 putative N-linked glycans in S protein expression, membrane fusion, entry, stability. Using α-glycosidase inhibitors castanospermine NB-DNJ, confirmed that disruption glycosylation blocked maturation protein, leading impairment protein-mediated fusion. Single-amino-acid substitution each sites with glutamine revealed 9 out were critical folding maturation. Thus, at these resulted reduced cell–cell fusion entry. Notably, N1074Q mutation markedly affected stability induced significant receptor-independent syncytium (RIS) formation HEK293T/hACE2-KO cells. Additionally, removal furin cleavage site partially compensated instability by mutation. Although corresponding SARS-CoV (N1056Q) did not induce RIS HEK293T cells, N669Q N1080Q mutants exhibited increased fusogenic activity Therefore, N-glycans on S2 subunits are highly important maintaining pre-fusion state protein. This study stability, information has implications design vaccines antiviral strategies.

Язык: Английский

Процитировано

2

Deep learning-based automatic segmentation of COVID-19 in chest X-ray images using ensemble neural net sentinel algorithm DOI Creative Commons

R. Catherine Junia,

K Selvan

Measurement Sensors, Год журнала: 2024, Номер 33, С. 101117 - 101117

Опубликована: Март 26, 2024

COVID-19 has affected billions of people worldwide and serious public health effects. Automatic image segmentation is crucial to improve clinical decision-making for full assessments illness management as well monitoring. It plays a part in detecting, diagnosing, tracking diseases by allowing the exact or accurate diseased regions. classifying medical images remains most difficult obstacle diagnosis, however, because lack annotated images. In this article, we propose Ensemble Neural Net Sentinel Algorithm (ENNSA), unique deep learning (DL) method classification COVID-19. Chest X-ray dataset first collected from Kaggle preprocessed. The features processed are retrieved using Insistent Grey Level Co-occurrence Matrix (IGLCM). suggested ENNSA outperforms current techniques terms accuracy (99.25), precision (100), recall (43), F1 score (61) regardless unbalanced datasets, indicating its promise diagnostic tool respiratory diseases. addition, approach used separate chosen chest investigational outcomes demonstrate that our proposed strategy currently methods

Язык: Английский

Процитировано

2