Understanding the cell Future views of structural biology

被引:12
|
作者
Beck, Martin [1 ,3 ]
Covino, Roberto [2 ]
Haenelt, Inga [3 ]
Mueller-McNicoll, Michaela [3 ]
机构
[1] Max Planck Inst Biophys, Max von Laue Str 3, D-60438 Frankfurt, Germany
[2] Frankfurt Inst Adv Studies, Ruth Moufang Str 1, D-60438 Frankfurt, Germany
[3] Goethe Univ Frankfurt, Frankfurt, Germany
关键词
LIQUID PHASE-SEPARATION; CRYOELECTRON TOMOGRAPHY; MOLECULAR SOCIOLOGY; PROTEIN FUNCTION; LIPID-BILAYERS; FORCE-FIELD; DYNAMICS; FLUORESCENCE; STATES; MECHANISMS;
D O I
10.1016/j.cell.2023.12.017
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
Determining the structure and mechanisms of all individual functional modules of cells at high molecular detail has often been seen as equal to understanding how cells work. Recent technical advances have led to a flush of high-resolution structures of various macromolecular machines, but despite this wealth of detailed information, our understanding of cellular function remains incomplete. Here, we discuss presentday limitations of structural biology and highlight novel technologies that may enable us to analyze molecular functions directly inside cells. We predict that the progression toward structural cell biology will involve a shift toward conceptualizing a 4D virtual reality of cells using digital twins. These will capture cellular segments in a highly enriched molecular detail, include dynamic changes, and facilitate simulations of molecular processes, leading to novel and experimentally testable predictions. Transferring biological questions into algorithms that learn from the existing wealth of data and explore novel solutions may ultimately unveil how cells work.
引用
收藏
页码:545 / 562
页数:18
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