Natural and artificial protein cages: design, structure and therapeutic applications

被引:48
作者
Heddle, Jonathan Gardiner [1 ]
Chakraborti, Soumyananda [1 ]
Iwasaki, Kenji [2 ]
机构
[1] Jagiellonian Univ, Bionanosci & Biochem Lab, Malopolska Ctr Biotechnol, Gronostajowa 7, PL-30387 Krakow, Poland
[2] Osaka Univ, Inst Prot Res, 3-2 Yamadaoka, Suita, Osaka, Japan
关键词
VIRUS-LIKE PARTICLES; BEAM-INDUCED MOTION; CRYOELECTRON MICROSCOPY; CRYO-EM; ELECTRON CRYOMICROSCOPY; BOVINE PAPILLOMAVIRUS; VIRAL NANOPARTICLES; ACCURATE DESIGN; DATA-BANK; VACCINE;
D O I
10.1016/j.sbi.2017.03.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Advanced electron microscopy techniques have been used to solve many viral capsid structures. The resulting detailed structural knowledge contributes to understanding of the mechanisms of self-assembly, maturation pathways and virion-host cell interactions. It also acts as inspiration for design and production of capsid-like artificial protein cages. Both natural and artificial cages have potential uses in medicine including as vaccines and in drug delivery. For vaccines, virus-like particles formed only from outer virion shells, lacking genetic material, offer the simplest basis for development, while encapsulation of target molecules inside protein cages is potentially more challenging. Here we review advances in cryo-electron microscopy with particular reference to viral capsid structures. We then consider why knowledge of these structures is useful, giving examples of their utilization as encapsulation and vaccine agents. Finally we look at the importance of structural techniques including cryo-EM in the rapidly progressing field of designed protein cages.
引用
收藏
页码:148 / 155
页数:8
相关论文
共 54 条
[1]   Paramagnetic viral nanoparticles as potential high-relaxivity magnetic resonance contrast agents [J].
Allen, M ;
Bulte, JWM ;
Liepold, L ;
Basu, G ;
Zywicke, HA ;
Frank, JA ;
Young, M ;
Douglas, T .
MAGNETIC RESONANCE IN MEDICINE, 2005, 54 (04) :807-812
[2]   Accurate design of megadalton-scale two-component icosahedral protein complexes [J].
Bale, Jacob B. ;
Gonen, Shane ;
Liu, Yuxi ;
Sheffler, William ;
Ellis, Daniel ;
Thomas, Chantz ;
Cascio, Duilio ;
Yeates, Todd O. ;
Gonen, Tamir ;
King, Neil P. ;
Baker, David .
SCIENCE, 2016, 353 (6297) :389-394
[3]   The Protein Data Bank [J].
Berman, HM ;
Westbrook, J ;
Feng, Z ;
Gilliland, G ;
Bhat, TN ;
Weissig, H ;
Shindyalov, IN ;
Bourne, PE .
NUCLEIC ACIDS RESEARCH, 2000, 28 (01) :235-242
[4]   Beam-induced motion of vitrified specimen on holey carbon film [J].
Brilot, Axel F. ;
Chen, James Z. ;
Cheng, Anchi ;
Pan, Junhua ;
Harrison, Stephen C. ;
Potter, Clinton S. ;
Carragher, Bridget ;
Henderson, Richard ;
Grigorieff, Nikolaus .
JOURNAL OF STRUCTURAL BIOLOGY, 2012, 177 (03) :630-637
[5]   Oxidative coupling of peptides to a virus capsid containing unnatural amino acids [J].
Carrico, Zachary M. ;
Romanini, Dante W. ;
Mehl, Ryan A. ;
Francis, Matthew B. .
CHEMICAL COMMUNICATIONS, 2008, (10) :1205-1207
[6]   Regulatory features of the trp operon and the crystal structure of the trp RNA-binding attenuation protein from Bacillus stearothermophilus [J].
Chen, XP ;
Antson, AA ;
Yang, M ;
Li, P ;
Baumann, C ;
Dodson, EJ ;
Dodson, GG ;
Gollnick, P .
JOURNAL OF MOLECULAR BIOLOGY, 1999, 289 (04) :1003-1016
[7]  
Chroboczek J, 2014, ACTA BIOCHIM POL, V61, P531
[8]  
Deshayes S, 2014, NANOMEDICINE-UK, V9, P1545, DOI [10.2217/NNM.14.67, 10.2217/nnm.14.67]
[9]   Cryo-EM of viruses and vaccine design [J].
Earl, Lesley A. ;
Subramaniam, Sriram .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2016, 113 (32) :8903-8905
[10]   Protein Calligraphy: A New Concept Begins To Take Shape [J].
Glover, Dominic J. ;
Clark, Douglas S. .
ACS CENTRAL SCIENCE, 2016, 2 (07) :438-444