ABSTRACT
With the ability to convert external excitation into heat, nanomaterials play an essential role in many biomedical applications. Two modes of nanoparticle (NP) array heating, nanoscale-confined heating (NCH) and macroscale-collective heating (MCH), have been found and extensively studied. Despite this, the resulting biological response at protein level remains elusive. In this study, we developed a computational model to systematically investigate the single-pulsed heating of NP array and corresponding protein denaturation/activation. We found that NCH may lead to targeted protein denaturation, however, nanoparticle heating does not lead to nanoscale selective TRPV1 channel activation. The excitation duration and NP concentration are primary factors that determine a window for targeted protein denaturation, and together with heating power, we defined quantified boundaries for targeted protein denaturation. Our results boost our understandings in the NCH and MCH under realistic physical constraints and provide a robust guidance to customize biomedical platforms with desired NP heating.
Competing Interest Statement
The authors have declared no competing interest.
ABBREVIATIONS
- NP
- nanoparticle;
- TRPV1
- transient receptor potential cation channel subfamily V member 1;
- NCH
- nanoscale-selective heating;
- MCH
- macroscale-collective heating;
- SLM
- spatial light modulation;
- ROS
- reactive oxygen species.
