Art in Research

Science is an art, but not all scientists are artists.

That said, we purposefully encourage our Biomedical Engineering students to express their creativity while showcasing their research.

Each fall, students submit images—photographs, micrographs, illustrations, visualizations and renderings—depicting their science, along with a description of how the image was created and how it represents the importance of research in their field. Art in Research is intended to be a record of striking visual qualities and a lens into the science, to be shared with fellow researchers and the general public alike.

A map of neural constellations

Submitted by: Lizzy Frazier

Category: Rendering

Contributors: Megan Lipton

Creation: Two-photon (2P) calcium images of neurons were obtained from the primary visual cortex of awake mice. Images were motion-corrected usingsuite2p. The mean image of neural activity was used as the basis for mapping "neural constellations."

Caption: Just as we map the constellations of the universe, we can map the constellations of the mind. Each neuron is a star, each connection a pathway through the universe of thought.

Cellular Symphony on Hydrogel

Submitted by: Tuba Marjan

Category: Microscopy

Creation: I created this image using fluorescent microscopy to capture mesenchymal stem cells growing on a 2D hydrogel scaffold. The cells were stained with phalloidin that binds to actin filaments which form the internal structure and give shape to the cell causing them to glow bright red. The nuclei were stained with Hoechst making them glow blue. The hydrogel allowed cells to adhere and spread out. This process blends scientific observation with a visual appreciation of cellular architecture where function meets form in a dynamic expression of life.

Endoplasmic reticulum (ER) dynamics at nanoscale

Submitted by: Yue Zheng

Category: Microscopy

Contributors: Li Fang, Maryam Mahmoodi, Hao-Cheng Gao, Fan Xu, Han Zhao & Fang Huang

Creation: Photoactivation localization microscopy (PALM) imaging of a living COS-7 cell stably expressing a HaloTag on reticulum 4(Rtn4) protein stained with PA-JF549-Halo. The raw single molecule blinking data was taken on a custom-built TIRF imaging system using a 405 nm laser for photoactivation and a 561 nm laser for excitation. Data was analyzed and reconstructed using the INSPR algorithm, and the localizations in 80 seconds were plotted through a jet (64) color map.

Caption: The structural changes and fast movements of ER tubules are clearly resolved at the nanometer scale of spatial resolution and seconds level of temporal resolution. The color from blue to red indicates the actual time from 0 to 80 seconds. The scale bar at the lower right is 500 nm.

Highway to the brain

Submitted by: Sergio Martin

Category: Anatomy & Physiology

Contributors: Thejas Vishnu Ramesh

Creation: This render was created from 4D Flow MRI data acquired at the Purdue 3T GE Discovery MR750 scanner. To obtain blood flow of the carotid bifurcation, a custom-made wearable coil was used. 4D flow MRI enables three-directional measurement of blood flow velocities over the cardiac cycle. Streamlines were generated from the MRI velocity field with the software Paraview, and overlaid over the structural image, acquired with time-of-flight MRI.

Caption: The image shows the flow of blood at the right carotid artery bifurcation. This section of the carotid splits from the common carotid artery into the internal and external carotid arteries, supplying blood to the brain, face, and head. 4D flow MRI can measure blood circulation in vivo, and it can be especially useful to assess vascular health and diseases. Custom-made coils for the neck result in a higher signal, improving the acquisitions of flow and resulting in more accurate velocity fields.

Microtubule tracks in neuronal growth cone

Submitted by: Yuan Ren

Category: Microscopy

Contributors: Donghan Ma, Kristi McElmurry, Fang Huang & Daniel M. Suter

Creation: Microtubules in Aplysia growth cone imaged with tubulin immunocytochemistry. DNA-PAINT, and super-resolution microscopy using custom-made single-molecule switching nanoscopy setup.

Caption: This image shows a multitude of parallel microtubules inside a growth cone of a cultured Aplysia neuron. Microtubules are essential for organelle transport, cell division, and cell motility.

Nuclear pore complexes under super-resolution microscope

Submitted by: Hao-Cheng Gao

Category: Microscopy

Contributors: Fan Xu

Creation: Immunolabeled cells was imaged with 4Pi single-molecule localization microscopy (4Pi-SMLM) and reconstruct its ultrastructure with nanometer resolution by using 4Pi-BRAINSPOT platform.

Caption: Nuclear pore complexes are massive protein assemblies embedded in the nuclear envelope that regulate the bidirectional transport of molecules between the nucleus and cytoplasm, playing a crucial role in cellular function and gene expression. Single-molecule localization microscopy (SMLM) surpasses the diffraction limit by precisely determining the positions of individual fluorophores, while 4Pi microscopy enhances achievable resolution through interferometric optical design. Together, 4Pi-SMLM facilitates 3D imaging of proteins with nanometer precision. The color code represents the depth (Z position) of the Nup96 proteins, as indicated by the color bar.

Progression of a Murine Thoracic Aortic Aneurysm

Submitted by: Ethan Kelley

Category: Anatomy & Physiology

Contributors: Courtland Johns

Creation: EKV (EKG-gated Kilohertz Visualization) Ultrasound Imaging

Caption: EKV ultrasound imaging visualizes the progression of a murine thoracic aortic aneurysm through five-time points after the introduction of BAPN (beta-aminopropionitrile) to drinking water. BAPN inhibits collagen replacement around major arteries, causing aneurysms when administered to young mice. Major tick marks indicate millimeters. Images were collected and processed with VisualSonics Vevo3100 and Vevo Lab.

Putting the P in Purdue: Precision Magnetic Bioassembly Using Microrobot Grippers

Submitted by: Madison Howard

Category: Anatomy & Physiology

Contributors: Aaron Davis

Creation: Fluorescent cancer cells and fibroblast spheroids were spatially patterned into a "P" shape using a microrobot gripper and imaged with a fluorescent microscope.

Caption: Cell spheroids were picked and placed in a "P" shape by a wireless, magnetic microrobot gripper.

Starry Night, Cell-estial Edition

Submitted by: Claudia Benito Alston

Category: Microscopy

Contributors: Michael Deines, Madison Howard & Evelyn Nonamaker

Creation: I cultured bone Messenchymal Stem Cells (bMSCs) for 14 days, after which I fixed and stained them with an Alkaline Phosphatase labeling kit.

Caption: Staining cells with alkaline phosphatase (ALP) is commonly used to assess cell differentiation, particularly in studies involving osteogenic (bone-forming) cells. ALP is an early marker of osteoblast differentiation, meaning it is expressed when precursor cells begin to differentiate into bone-forming osteoblasts. By staining cells for ALP, we can visually confirm and quantify the activity of these cells as they progress along the osteogenic pathway.

The Human Operating System

Submitted by: Hammad Khan

Category: Rendering

Creation: Illustrator, Imagej, Device Fabrication, Neural Recordings

Caption: Created from real neural data and biophysical reconstructions of neural connections, this piece represents the next frontier for neurotechnology and physiology. Technological breakthroughs will augment dynamic models between muscles, nerves, and neurons to understand the basis for intelligence.

The Spider-Verse Within You

Submitted by: Makayla Phillips

Category: Microscopy

Contributors: Josh Sexton, Sherry Harbin & Rachel Morrison

Creation: The image was captured using a confocal microscope to analyze an immunofluorescent stained transverse muscle cross-section

Caption: An immunofluorescent laminin stain under a confocal microscope