Biological Insight from Super-Resolution Microscopy: What We Can Learn from Localization-Based Images

被引:133
作者
Baddeley, David [1 ,2 ]
Bewersdorf, Joerg [1 ,3 ]
机构
[1] Yale Sch Med, Dept Cell Biol, New Haven, CT 06520 USA
[2] Univ Auckland, Auckland Bioengn Inst, Auckland 1010, New Zealand
[3] Yale Univ, Dept Biomed Engn, New Haven, CT 06520 USA
来源
ANNUAL REVIEW OF BIOCHEMISTRY, VOL 87 | 2018年 / 87卷
基金
英国惠康基金; 美国国家卫生研究院;
关键词
single-molecule localization microscopy; nanoscopy; quantitative analysis; PALM; STORM; PAINT; 3-DIMENSIONAL LOCALIZATION; QUANTITATIVE-ANALYSIS; SINGLE MOLECULES; CLUSTER-ANALYSIS; IMAGING REVEALS; RESOLUTION; PROTEINS; TRACKING; NANOSCOPY; ARTIFACTS;
D O I
10.1146/annurev-biochem-060815-014801
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
Super-resolution optical imaging based on the switching and localization of individual fluorescent molecules [photoactivated localization microscopy (PALM), stochastic optical reconstruction microscopy (STORM), etc.] has evolved remarkably over the last decade. Originally driven by pushing technological limits, it has become a tool of biological discovery. The initial demand for impressive pictures showing well-studied biological structures has been replaced by a need for quantitative, reliable data providing dependable evidence for specific unresolved biological hypotheses. In this review, we highlight applications that showcase this development, identify the features that led to their success, and discuss remaining challenges and difficulties. In this context, we consider the complex topic of defining resolution for this imaging modality and address some of the more common analytical methods used with this data.
引用
收藏
页码:965 / 989
页数:25
相关论文
共 110 条
[91]   Wide-field subdiffraction imaging by accumulated binding of diffusing probes [J].
Sharonov, Alexey ;
Hochstrasser, Robin M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (50) :18911-18916
[92]   Super-resolution microscopy reveals that disruption of ciliary transition-zone architecture causes Joubert syndrome [J].
Shi, Xiaoyu ;
Garcia, Galo, III ;
Van De Weghe, Julie C. ;
McGorty, Ryan ;
Pazour, Gregory J. ;
Doherty, Dan ;
Huang, Bo ;
Reiter, Jeremy F. .
NATURE CELL BIOLOGY, 2017, 19 (10) :1178-+
[93]   On spectroscopic resolving power [J].
Sparrow, CM .
ASTROPHYSICAL JOURNAL, 1916, 44 (02) :76-86
[94]   Frontiers in structured illumination microscopy [J].
Strtoehl, Florian ;
Kaminski, Clemens F. .
OPTICA, 2016, 3 (06) :667-677
[95]   Nuclear Pore Scaffold Structure Analyzed by Super-Resolution Microscopy and Particle Averaging [J].
Szymborska, Anna ;
de Marco, Alex ;
Daigle, Nathalie ;
Cordes, Volker C. ;
Briggs, John A. G. ;
Ellenberg, Jan .
SCIENCE, 2013, 341 (6146) :655-658
[96]   Long time-lapse nanoscopy with spontaneously blinking membrane probes [J].
Takakura, Hideo ;
Zhang, Yongdeng ;
Erdmann, Roman S. ;
Thompson, Alexander D. ;
Lin, Yu ;
McNellis, Brian ;
Rivera-Molina, Felix ;
Uno, Shin-nosuke ;
Kamiya, Mako ;
Urano, Yasuteru ;
Rothman, James E. ;
Bewersdorf, Joerg ;
Schepartz, Alanna ;
Toomre, Derek .
NATURE BIOTECHNOLOGY, 2017, 35 (08) :773-780
[97]   A trans-synaptic nanocolumn aligns neurotransmitter release to receptors [J].
Tang, Ai-Hui ;
Chen, Haiwen ;
Li, Tuo P. ;
Metzbower, Sarah R. ;
MacGillavry, Harold D. ;
Blanpied, Thomas A. .
NATURE, 2016, 536 (7615) :210-+
[98]   Precise nanometer localization analysis for individual fluorescent probes [J].
Thompson, RE ;
Larson, DR ;
Webb, WW .
BIOPHYSICAL JOURNAL, 2002, 82 (05) :2775-2783
[99]   New concepts in synaptic biology derived from single-molecule imaging [J].
Triller, Antoine ;
Choquet, Daniel .
NEURON, 2008, 59 (03) :359-374
[100]   Single-particle electron cryo-microscopy: towards atomic resolution [J].
van Heel, M ;
Gowen, B ;
Matadeen, R ;
Orlova, EV ;
Finn, R ;
Pape, T ;
Cohen, D ;
Stark, H ;
Schmidt, R ;
Schatz, M ;
Patwardhan, A .
QUARTERLY REVIEWS OF BIOPHYSICS, 2000, 33 (04) :307-369