High pressure macromolecular crystallography (HPMX) is an ideal technique to trap high-energy transient conformers of proteins that are essential for biological activity and/or for interaction with partners. Using a diamond anvil cell (DAC) and collecting data at room temperature (RT) ensures that the pressure/temperature of the sample environment is precisely defined and controlled. For proteins, this usually requires large enough crystals to collect a complete data set at high resolution, hopefully radiation damage free. However, growing such crystals remain a challenge. Serial crystallography offers the possibility to collect diffraction data from micron-sized crystals at RT. Indeed, only a single diffraction frame is recorded from a small single crystal, therefore spreading the required X-ray dose to reconstruct a complete dataset over a very large number of micron-sized crystals. we want to evaluate the feasibility to combine SX and DAC techniques to push forward HPMX.