ForceGen: End-to-end de novo protein generation based on nonlinear mechanical unfolding responses using a language diffusion model

被引:19
作者
Ni, Bo [1 ]
Kaplan, David L. [2 ]
Buehler, Markus J. [1 ,3 ]
机构
[1] MIT, Lab Atomist & Mol Mech LAMM, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[2] Tufts Univ, Dept Biomed Engn, Medford, MA 02155 USA
[3] MIT, Schwarzman Coll Comp, Ctr Computat Sci & Engn, 77 Massachusetts Ave, Cambridge, MA 02139 USA
关键词
SECONDARY STRUCTURE; NANOMECHANICS; SOLUBILITY; PREDICTION; SILK; DYNAMICS; DESIGN; PORTER; FIELDS;
D O I
10.1126/sciadv.adl4000
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Through evolution, nature has presented a set of remarkable protein materials, including elastins, silks, keratins and collagens with superior mechanical performances that play crucial roles in mechanobiology. However, going beyond natural designs to discover proteins that meet specified mechanical properties remains challenging. Here, we report a generative model that predicts protein designs to meet complex nonlinear mechanical property-design objectives. Our model leverages deep knowledge on protein sequences from a pretrained protein language model and maps mechanical unfolding responses to create proteins. Via full-atom molecular simulations for direct validation, we demonstrate that the designed proteins are de novo, and fulfill the targeted mechanical properties, including unfolding energy and mechanical strength, as well as the detailed unfolding force-separation curves. Our model offers rapid pathways to explore the enormous mechanobiological protein sequence space unconstrained by biological synthesis, using mechanical features as the target to enable the discovery of protein materials with superior mechanical properties.
引用
收藏
页数:15
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