Structure of Adenovirus Type 21 Knob in Complex with CD46 Reveals Key Differences in Receptor Contacts among Species B Adenoviruses

Author:

Cupelli Karolina1,Müller Steffen1,Persson B. David1,Jost Marco1,Arnberg Niklas2,Stehle Thilo13

Affiliation:

1. Interfaculty Institute for Biochemistry, University of Tübingen, D-72076 Tübingen, Germany

2. Division of Virology, Department of Clinical Microbiology, Laboratory for Molecular Infection Medicine in Sweden, Umeå University, SE-901 85 Umeå, Sweden

3. Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, Tennessee 37232

Abstract

ABSTRACT The complement regulation protein CD46 is the primary attachment receptor for most species B adenoviruses (Ads). However, significant variability exists in sequence and structure among species B Ads in the CD46-binding regions, correlating with differences in affinity. Here, we report a structure-function analysis of the interaction of the species B Ad21 knob with the two N-terminal repeats SCR1 and SCR2 of CD46, CD46-D2. We have determined the structures of the Ad21 knob in its unliganded form as well as in complex with CD46-D2, and we compare the interactions with those observed for the Ad11 knob-CD46-D2 complex. Surface plasmon resonance measurements demonstrate that the affinity of Ad21 knobs for CD46-D2 is 22-fold lower than that of the Ad11 knob. The superposition of the Ad21 and Ad11 knob structures in complex with CD46-D2 reveals a substantially different binding mode, providing an explanation for the weaker binding affinity of the Ad21 knob for its receptor. A critical difference in both complex structures is that a key interaction point, the DG loop, protrudes more in the Ad21 knob than in the Ad11 knob. Therefore, the protruding DG loop does not allow CD46-D2 to approach the core of the Ad21 knob as closely as in the Ad11 knob-CD46-D2 complex. In addition, the engagement of CD46-D2 induces a conformational change in the DG loop in the Ad21 knob but not in the Ad11 knob. Our results contribute to a more profound understanding of the CD46-binding mechanism of species B Ads and have relevance for the design of more efficient gene delivery vectors.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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