Anton Poliakov
University of Alabama at Birmingham
10 Papers
55 Citations
Anton Poliakov is an academic researcher from University of Alabama at Birmingham. The author has contributed to research in topics: Mass spectrometry & Hydrogen–deuterium exchange. The author has an hindex of 8, co-authored 10 publications. Previous affiliations of Anton Poliakov include University of Alabama.
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Papers
Induction of myeloid-derived suppressor cells by tumor exosomes
Xiaoyu Xiang,Anton Poliakov,Cunren Liu,Yuelong Liu,Zhongbin Deng,Jianhua Wang,Ziqiang Cheng,Spandan V. Shah,Gui-Jun Wang,Liming Zhang,William E. Grizzle,James A. Mobley,Huang-Ge Zhang,Huang-Ge Zhang +13 more
TL;DR: These findings lend themselves to developing specific targetable therapeutic strategies to reduce or eliminate MDSC‐induced immunosuppression and hence enhance host antitumor immunotherapy efficacy.
Adipose Tissue Exosome-Like Vesicles Mediate Activation of Macrophage-Induced Insulin Resistance
Zhongbin Deng,Anton Poliakov,Robert W. Hardy,Ronald H. Clements,Cunren Liu,Yuelong Liu,Jianhua Wang,Xiaoyu Xiang,Shuangqin Zhang,Xiaoying Zhuang,Spandan V. Shah,Dongmei Sun,Sue Michalek,William E. Grizzle,Timothy W Garvey,James A. Mobley,Huang-Ge Zhang +16 more
TL;DR: ELVs released by adipose tissue can act as a mode of communication between adipose tissues and macrophages and insulin resistance requires the TLR4/TRIF pathway.
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Structural heterogeneity and protein composition of exosome-like vesicles (prostasomes) in human semen.
TL;DR: Human seminal fluid contains small exosome‐like vesicles called prostasomes, which play an important role in the process of fertilization by boosting survivability and motility of spermatozoa, in addition to modulating acrosomal reactivity.
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Capsid Size Determination by Staphylococcus aureus Pathogenicity Island SaPI1 Involves Specific Incorporation of SaPI1 Proteins into Procapsids
Anton Poliakov,Jenny R. Chang,Michael S. Spilman,Priyadarshan K. Damle,Gail E. Christie,James A. Mobley,Terje Dokland +6 more
TL;DR: Mass spectrometry on full-length phage proteins showed that the major capsid protein and the scaffolding protein are N-terminally processed in both 80alpha and SaPI1 procapsids.
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Incorporation of scaffolding protein gpO in bacteriophages P2 and P4.
TL;DR: Protein analysis and mass spectroscopy are used to show that P2 and P4 virions as well as procapsids isolated from viral infections contain O(*) and that cleavage occurs between residues 141 and 142 of gpO.
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