Kramarska相关文献与解析，生知库 | 链接生命科学的每一步

Identification of cross-reactive vaccine antigen candidates in Gram-positive ESKAPE pathogens through subtractive proteome analysis using opsonic sera.

利用调理血清进行减法蛋白质组分析，鉴定革兰氏阳性 ESKAPE 病原体中的交叉反应疫苗抗原候选物

doi:10.1371/journal.pone.0319933

Sadones OcÃ©ane, Kramarska Eliza, Sainz-MejÃas Maite, Berisio Rita, Huebner Johannes, McClean SiobhÃ¡n, Romero-Saavedra Felipe

其它

发表日期：2025

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Crystal structure and biophysical characterisation of the enterococcal foldase PpiC, a cross-opsonic antigen against gram-positive nosocomial pathogens

肠球菌折叠酶 PpiC 的晶体结构和生物物理特性，一种针对革兰氏阳性医院感染病原体的交叉调理抗原

期刊:

影响因子:

doi:10.1111/febs.70160

Napolitano, Valeria; Kramarska, Eliza; Ghilardi, Ornella; Romero-Saavedra, Felipe; Del Vecchio, Pompea; Squeglia, Flavia; Huebner, Johannes; Berisio, Rita

A rationally designed antigen elicits protective antibodies against multiple nosocomial Gram-positive pathogens

一种经过合理设计的抗原可诱导产生针对多种医院感染革兰氏阳性病原体的保护性抗体。

期刊:NPJ Vaccines

影响因子:6.5

doi:10.1038/s41541-024-00940-x

Kramarska, Eliza; Toumi, Eya; Squeglia, Flavia; Laverde, Diana; Napolitano, Valeria; Frapy, Eric; Autiero, Ida; Sadones, Oceane; Huebner, Johannes; Skurnik, David; Romero-Saavedra, Felipe; Berisio, Rita

Investigation of cross-opsonic effect leads to the discovery of PPIase-domain containing protein vaccine candidate to prevent infections by Gram-positive ESKAPE pathogens

对交叉调理效应的研究发现了一种含有PPIase结构域的蛋白质疫苗候选物，该疫苗可预防革兰氏阳性ESKAPE病原体的感染。

期刊:BMC Microbiology

影响因子:4.2

doi:10.1186/s12866-024-03427-w

Sadones, Océane; Kramarska, Eliza; Laverde, Diana; Berisio, Rita; Huebner, Johannes; Romero-Saavedra, Felipe

A Structural View at Vaccine Development against M. tuberculosis

结核分枝杆菌疫苗研发的结构视角

期刊:Cells

影响因子:5.2

doi:10.3390/cells12020317

Romano, Maria; Squeglia, Flavia; Kramarska, Eliza; Barra, Giovanni; Choi, Han-Gyu; Kim, Hwa-Jung; Ruggiero, Alessia; Berisio, Rita

发表日期：2023

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Klebsiella phage KP34gp57 capsular depolymerase structure and function: from a serendipitous finding to the design of active mini-enzymes against K. pneumoniae

克雷伯氏菌噬菌体 KP34gp57 荚膜解聚酶的结构和功能：从偶然发现到针对肺炎克雷伯氏菌的活性微酶的设计

期刊:mBio

影响因子:5.1

doi:10.1128/mbio.01329-23

Barbara Maciejewska #, Flavia Squeglia #, Agnieszka Latka, Mario Privitera, Sebastian Olejniczak, Paulina Switala, Alessia Ruggiero, Daniela Marasco, Eliza Kramarska, Zuzanna Drulis-Kawa, Rita Berisio

Versatile and Easily Designable Polyester-Laser Toner Interfaces for Site-Oriented Adsorption of Antibodies

多功能且易于设计的聚酯激光碳粉界面，用于抗体的位点吸附

期刊:International Journal of Molecular Sciences

影响因子:0.7

doi:10.3390/ijms23073771

Marcin Drozd, Polina Ivanova, Katarzyna Tokarska, Kamil Żukowski, Aleksandra Kramarska, Adam Nowiński, Ewa Kobylska, Mariusz Pietrzak, Zbigniew Brzózka, Elżbieta Malinowska

发表日期：2022

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PE_PGRS3 ensures provision of the vital phospholipids cardiolipin and phosphatidylinositols by promoting the interaction between M. tuberculosis and host cells

PE_PGRS3 通过促进结核分枝杆菌与宿主细胞之间的相互作用来确保提供重要的磷脂心磷脂和磷脂酰肌醇

期刊:Virulence

影响因子:5.5

doi:10.1080/21505594.2021.1897247

Flavio De Maio, Alessandro Salustri, Basem Battah, Ivana Palucci, Federica Marchionni, Silvia Bellesi, Valentina Palmieri, Massimiliano Papi, Eliza Kramarska, Maurizio Sanguinetti, Michela Sali, Rita Berisio, Giovanni Delogu

PE_PGRS33, an Important Virulence Factor of Mycobacterium tuberculosis and Potential Target of Host Humoral Immune Response

PE_PGRS33是结核分枝杆菌的重要毒力因子，也是宿主体液免疫反应的潜在靶点。

期刊:Cells

影响因子:5.2

doi:10.3390/cells10010161

Kramarska, Eliza; Squeglia, Flavia; De Maio, Flavio; Delogu, Giovanni; Berisio, Rita

A Self-Assembling Cross-Protective Antigen Against Multiple Gram-Positive Nosocomial Pathogens

一种可自组装的、针对多种革兰氏阳性医院感染病原体的交叉保护性抗原

Identification of cross-reactive vaccine antigen candidates in Gram-positive ESKAPE pathogens through subtractive proteome analysis using opsonic sera.

利用调理血清进行减法蛋白质组分析，鉴定革兰氏阳性 ESKAPE 病原体中的交叉反应疫苗抗原候选物

Crystal structure and biophysical characterisation of the enterococcal foldase PpiC, a cross-opsonic antigen against gram-positive nosocomial pathogens

肠球菌折叠酶 PpiC 的晶体结构和生物物理特性，一种针对革兰氏阳性医院感染病原体的交叉调理抗原

A rationally designed antigen elicits protective antibodies against multiple nosocomial Gram-positive pathogens

一种经过合理设计的抗原可诱导产生针对多种医院感染革兰氏阳性病原体的保护性抗体。

Investigation of cross-opsonic effect leads to the discovery of PPIase-domain containing protein vaccine candidate to prevent infections by Gram-positive ESKAPE pathogens

对交叉调理效应的研究发现了一种含有PPIase结构域的蛋白质疫苗候选物，该疫苗可预防革兰氏阳性ESKAPE病原体的感染。

A Structural View at Vaccine Development against M. tuberculosis

结核分枝杆菌疫苗研发的结构视角

Klebsiella phage KP34gp57 capsular depolymerase structure and function: from a serendipitous finding to the design of active mini-enzymes against K. pneumoniae

克雷伯氏菌噬菌体 KP34gp57 荚膜解聚酶的结构和功能：从偶然发现到针对肺炎克雷伯氏菌的活性微酶的设计

Versatile and Easily Designable Polyester-Laser Toner Interfaces for Site-Oriented Adsorption of Antibodies

多功能且易于设计的聚酯激光碳粉界面，用于抗体的位点吸附

PE_PGRS3 ensures provision of the vital phospholipids cardiolipin and phosphatidylinositols by promoting the interaction between M. tuberculosis and host cells

PE_PGRS3 通过促进结核分枝杆菌与宿主细胞之间的相互作用来确保提供重要的磷脂心磷脂和磷脂酰肌醇

PE_PGRS33, an Important Virulence Factor of Mycobacterium tuberculosis and Potential Target of Host Humoral Immune Response

PE_PGRS33是结核分枝杆菌的重要毒力因子，也是宿主体液免疫反应的潜在靶点。