Structure and dynamics of an α-fucosidase reveal a mechanism for highly efficient IgG transfucosylation.

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作者： Erik H,Klontz ^[1] ; Chao,Li ^[2] ; Kyle,Kihn ^[3] ; James K,Fields ^[4] ; Dorothy,Beckett ^[5] ; Greg A,Snyder ^[1] ; Patrick L,Wintrode ^[2] ; Daniel,Deredge ^[3] ; Lai-Xi,Wang ^[4] ; Eric J,Sundberg ^[1]

作者单位： Institute of Human Virology, University of Maryland School of Medicine, Baltimore, MD, 21201, USA. ^[1] Department of Microbiology & Immunology, University of Maryland School of Medicine, Baltimore, MD, 21201, USA. ^[2] Program in Molecular Microbiology & Immunology, University of Maryland School of Medicine, Baltimore, MD, 21201, USA. ^[3] Department of Chemistry and Biochemistry, University of Maryland, College Park, MD, 20742, USA. ^[4] Department of Pharmaceutical Sciences, University of Maryland School of Pharmacy, College Park, MD, 21201, USA. ^[5] Institute of Human Virology, University of Maryland School of Medicine, Baltimore, MD, 21201, USA. eric.sundberg@emory.edu. ^[6] Department of Microbiology & Immunology, University of Maryland School of Medicine, Baltimore, MD, 21201, USA. eric.sundberg@emory.edu. ^[7] Department of Medicine, University of Maryland School of Medicine, Baltimore, MD, 21201, USA. eric.sundberg@emory.edu. ^[8] Department of Biochemistry, Emory University School of Medicine, Atlanta, GA, 30322, USA. eric.sundberg@emory.edu. ^[9]