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马菱蔓
职称:副教授
邮箱:1620174416@cpu.edu.cn
学院:生命科学与技术学院
实验室:江宁校区学院实验楼一期317-1室
招生学科:微生物与生化药学,生物与医药,生物学
办公室:江宁校区学院实验楼一期315室
个人简历

马菱蔓,1987年生,生命科学与技术学院微生物学教研室,一直致力于抗耐药性病原微生物药物作用机制(靶点)的相关研究;同时,具备丰富的多肽结构设计和构效优化经验。主要研究方向:(1病原菌-宿主互作研究;(2)抗耐药细菌感染药物的活性评价及分子机制研究。近年来,主持国家自然科学基金青年项目江苏省自然科学基金青年项目、中国博士后面上/特别资助(站中)项目及江苏省科协青年科技人才托举工程资助培养项目等,同时参与多项国家和省部级科研项目。目前,在相关研究领域的主流期刊上以第一作者或通讯作者发表SCI研究论文20,申请发明专利5

 


研究方向

抗感染药理

 


主持在研项目情况

[1] 国家自然科学基金青年项目,81803591,构效优化的新型抗菌肽MSI-1抗耐甲氧西林金黄色葡萄球菌的机制研究,2019/01-2021/1221.9万元,主持

[2] 江苏省自然科学基金青年项目,BK20180563,新型抗耐药菌多肽MSI-1的活性及机制研究,2018/07-2021/620万元,主持

[3] 中国博士后科学基金第13批特别资助(站中),2020T130723,基于MCR-1靶点的抗菌肽MSI-1mcr-1多粘菌素耐药感染的分子机制,2020/01-2021/1218万元,主持

[4] 中央高校基本业务费(重点项目),2632021ZD07,抗菌肽 MSI-1 通过干预 MCR-1 对细菌 Lipid A 的修饰抑制mcr-1多黏菌素耐药细菌免疫逃逸的机制研究,2021/01-2022/1215万元,主持

[5] 江苏省科协,tj12882020年江苏省科协青年科技人才托举工程资助培养项目,2020/08-2022/063万元,主持

[6] 中国博士后科学基金第62批面上资助,1600010009,基于宿主防御的多肽抗H. pylori感染的机制研究,2018/01-2020/015 万元,主持

[7] 十三五重大新药创制科技重大专项(耐药菌防治药物品种及共性关键技术研发), 2019ZX09721001-004-005I类新药抗真菌多肽PL-18和抗耐药菌多肽Cbf-14临床前研究,2019/01-2021/12244.42万元,骨干成员,划拨经费30万元

[8] 国家自然科学基金面上项目82173863,基于MCR-1修饰LPS介导的细菌免疫逃逸探讨新结构多肽MSI-1抗多黏菌素耐药感染的机制,2022/01-2025/1255 万元,骨干成员,划拨经费25

[9] 国家自然科学基金面上项目,81673483,基于多靶点的多肽抗耐药性细菌感染的机制研究,2017/01-2020/1245万元,骨干成员,划拨经费20万元

近年代表性科研成果

[1] Xinyue Ye, Jian Wang, Pengfei Xu, Xiaoqian Yang, Qixue Shi, Genyan Liu, Zhaoshi Bai, Changlin Zhou*, Lingman Ma*, Peptide MSI- 1 inhibited MCR- 1 and regulated outer membrane vesicles to combat immune evasion of Escherichia coli. Microbial Biotechnology. 2023; 16:1755-1773.

[2] Liping Wang, Mengyuan Liu, Yixin Qi, Jian Wang, Qixue Shi, Xiaolin Xie, Changlin Zhou*, Lingman Ma*. hsdSA regulated extracellular vesicle-associated PLY to protect Streptococcus pneumoniae from macrophage killing via LAPosomes. Microbiol Spectr. 2024 Jan 11;12(1): e0099523.[3] Ye Xinyue#, Huang Ya#, Zhou Chenyu, Liu Xiaoyun, Zhao Wenxuan, Zhao Xiurong, Xie Xiaolin, Wang Liping, Bai Zhaoshi*, Zhou Changlin*, Ma Lingman*. MSI-1 combats drug-resistant S. aureus by affecting bacterial viability and inhibiting carotenoid pigment production. Microbiological Research. 2021 Oct 27; 255: 126909.

[4] Bo Huang, Zhaoshi Bai*, Xinyue Ye, Chenyu Zhou, Xiaolin Xie, Yuejiao Zhong, Kejiang Lin*, Lingman Ma*. Structural analysis and binding sites of inhibitors targeting the CD47/SIRPα interaction in anticancer therapy. Comput Struct Biotechnol J. 2021 Oct 1;19:5494-5503.

[5] Zhaoshi Bai, Qing Zhou, Huayun Zhu, Xinyue Ye, Pingping Wu*, Lingman Ma*. QTMP, a Novel Thiourea Polymer, Causes DNA Damage to Exert Anticancer Activity and Overcome Multidrug Resistance in Colorectal Cancer Cells. Front Oncol. 2021 May 28;11:667689.

[6] Lingman Ma#, Xinyue Ye#, Pengbo Sun, Pengfei Xu, Liping Wang, Zixiang Liu, Xiaowei Huang, Zhaoshi Bai*, Changlin Zhou*, Antimicrobial and antibiofilm activity of the EeCentrocin 1 derived peptide EC1-17KV via membrane disruption, EBioMedicine, 2020, 55: 102775.

[7] Lingman Ma#, Xin Xie#, Hanhan Liu, Ya Huang, Haomin Wu, Meiling Jiang, Pengfei Xu, Xinyue Ye, Changlin Zhou*, Potent antibacterial activity of MSI-1 derived from the magainin 2 peptide against drug-resistant bacteria, Theranostics, 2020, 10(3):1373-1390.

[8] Meiling Jiang, Xiaoqian Yang, Haomin Wu, Ya Huang, Jie Dou, Changlin Zhou*, Lingman Ma*, An active domain HF-18 derived from hagfish intestinal peptide effectively inhibited drug-resistant bacteria in vitro/vivo, Biochemical Pharmacology, 2020, 172: 113746.

[9] Qian Yu#, Minda Zhang#, Qidi Ying, Xin Xie, Shuwen Yue, Qing Wei, Zhaoshi Bai*, Lingman Ma*. Decrease of AIM2 mediated by luteolin contributes to non-small cell lung cancer treatment. Cell Death & Disease. 2019 Mar 4;10(3):218.

[10] Lingman Ma, Yanrong Wang, Mengxiao Wang, Yuwei Tian, Wei Kang, Hanhan Liu, Hui Wang, Jie Dou*, Changlin Zhou*, Effective antimicrobial activity of Cbf-14, derived from a cathelin-like domain, against penicillin-resistant bacteria, Biomaterials, 2016, 87:32-45.