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Yi-Feng Shi

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Articles by Yi-Feng Shi

Comparing Non-Covalent and Covalent Docking Simulations of Cyclic Boronate Inhibitors Against KPC Serine Carbapenemase

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By Yi-Feng Shi
| Preprints.org
Submitted: 04 October 2026 You are already at the latest version The spread of carbapenem-resistant Enterobacteriaceae (CRE) has weakened control of severe hospital infections. These strains evade nearly all last-resort antibiotics, making targeted β-lactamase inhibitors indispensable for β-lactam treatment. Existing carbapenem-bicyclic boronate derivative combinations show broad-spectrum activity, with confirmed efficacy against Class A serine carbapenemases represented by KPC-2.
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Ubiquitination of ACSL4 by Parkin Suppresses Ferroptosis and Rescues Glucocorticoid-Induced Bone Loss

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By Li-jiang Han, Yi-Feng Shi, Jian-sen Miao
| Wiley Online Library Verified
1 Introduction Glucocorticoids (GCs) are widely used as anti-inflammatory and immunosuppressive agents in clinical practice for the treatment of various autoimmune diseases, inflammatory disorders, and organ transplant rejection [1]. However, long-term or high-dose GCs use leads to serious skeletal complications, the most typical of which is glucocorticoids-induced osteoporosis (GIOP) [2].
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Exploring PBP2a resistance in MRSA by comparison between molecular covalent docking and non-covalent docking

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By Yi-Feng Shi, Dalian Polytechnic, Ye-Qiang Cao
| BioRxiv
Abstract Background and objectives: The presence of penicillin-binding protein 2a (PBP2a) is the cause of Methicillin-resistant Staphylococcus aureus (MRSA), which is important nosocomial pathogens worldwide and now are also of growing importance in community-acquired infection. The PBP2a resistance depends upon a supplementary peptidoglycan transpeptidase, which continues to function when normal PBPs have been inactivated by beta-lactam antibiotics.
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Non-covalent Linking Antibody to Yeast Using the Cell Surface Display of Staphylococcal Protein A

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By Yi-Feng Shi, Dalian Polytechnic
| BioRxiv
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