J. Richard McIntosh is a Distinguished Professor Emeritus in Molecular, Cellular, and Developmental Biology at the University of Colorado Boulder. McIntosh first graduated from Harvard with a BA in Physics in 1961, and again with a Ph.D. in Biophysics in 1968. He began his teaching career at Harvard but has spent most of his career at the University of Colorado Boulder. At the University of Colorado Boulder, McIntosh taught biology courses at both the undergraduate and graduate levels. Additionally, he created an undergraduate course in the biology of cancer towards the last several years of his teaching career. McIntosh's research career looks at a variety of things, including different parts of mitosis, microtubules, and motor proteins.
Research interests
Mitosis Most of McIntosh's work focuses on the process of mitosis in the cell. Mitosis is the process of cell division that includes distinct movements of chromosomes in the cell and formation of mitotic spindles. Additionally, McIntosh is very interested in the role of microtubules and motor proteins in this process. Mitotic spindles, composed of microtubules and other proteins, ensure that each of the two new cells during cell division both get one copy of every chromosome. After the chromosomes are separated, then the cells are able to completely separate as well through cytokinesis. In mitosis, there are multiple phases. In prophase, the DNA starts to package itself for division and microtubules reorganize to prepare to form the mitotic spindle. In prometaphase, kinetochores develop where the chromosome will attach to the mitotic spindle. After that, chromosomes move towards the middle of the cell (metaphase plate) and the two copies separate during anaphase. In some of McIntosh's work he looks specifically at the anaphase A portion, which is related to where the chromosome is in relation to the pole it is moving towards. Lastly, in telophase, the cell is wrapping up the stages of mitosis with creating a new nuclear envelope.
Use of electron tomography Additionally, in many of the works outlined below, McIntosh commonly uses electron tomography to image and study the cells. In electron tomography, many different images are put together to create a 3D image of the subject being studied. This technology is best suited to observe extremely complex structures and can image thinner sections of samples than can be physically made to study.
1970s and 1980s One of McIntosh's earlier studies in the field of cell biology is in 1974, where his team published a paper on the structures of flagella of Pyrsonympha, an organism found in termites. In this work, his team described the axostyle, a collection of microtubules, and presented that the axostyle's attachment to other parts of the cell controls its function.
In 1980, McIntosh's curiosity with microtubules continued in "Visualization of the structural polarity of microtubules". The polarity of microtubules is essential to generate the force needed to separate the chromosomes during mitosis, but at the time it was difficult to determine what the polarity is. McIntosh's team uses basal bodies and HeLa cells to study how protofilaments 'hook' onto them—either in right-handedness or left-handedness—in vitro to determine polarity.
A few years later, McIntosh published a study in 1984 on how tubulin moves in mammalian cells with a focus on the cell cycle. To study the movements in tubulin in cells during mitosis and interphase, McIntosh used two imaging methods: labeled (dichlorotriazinyl-aminofluorescein or DTAF-) tubulin and fluorescence redistribution (or recovery) after photobleaching (or FRAP). Using the labeled tubulin, McIntosh observed how quickly the freely-added labeled tubulin was polymerized to the existing microtubule structures in the cell. It was noted that measuring the tubulin addition in interphase was difficult due to the lack of structures, while it was more observable in a mitotic cell. While using FRAP, McIntosh noticed that the tubulin redistributed throughout the cytoplasm in both a rapid phase as well as a slower phase. Overall, the redistribution or movement of the labeled tubulin in cells undergoing mitosis was much faster than the redistribution observed for cells in interphase. The next year, McIntosh's interests started to shift towards motor proteins. Kinesin, a motor protein found to move around vesicles in the cell, was recently discovered on another paper published the same year. Here, McIntosh explored the possibility of kinesin as an important part of mitosis, as it can be found in the mitotic spindle. Some of the possible functions that McIntosh suggested kinesin may have in mitosis are that they move chromosomes down microtubules or move microtubules in different areas within the mitotic spindle.
The next year, McIntosh's interests started to shift towards motor proteins. Kinesin, a motor protein found to move around vesicles in the cell, was recently discovered on another paper published the same year. Here, McIntosh explored the possibility of kinesin as an important part of mitosis, as it can be found in the mitotic spindle. Some of the possible functions that McIntosh suggested kinesin may have in mitosis are that they move chromosomes down microtubules or move microtubules in different areas within the mitotic spindle.
1990s McIntosh's interest in the connection of motor proteins and mitosis continues into the 1990s. In 1990, he published a paper on cytoplasmic dynein and mitosis. Dynein, a protein first found in the flagella, had now been discovered in the cytoplasm as well. It moves towards the minus end, or the slower-growing end, of the microtubules. The research team used antibodies to image the distribution of cytoplasmic dynein in the cell. Dynein was found to be near kinetochores during mitosis, while in interphase they were scattered around the cell. The research team used this finding to suggest that dynein had a role in how chromosomes separate during mitosis due to the spatial differences of dynein during interphase and mitosis.
In contrast to the topics McIntosh had researched so far, in 1996 his team published "Computer Visualization of Three-Dimensional Image Data using IMOD." In this article, his team shared the development of the computer software called IMOD. With IMOD, researchers can study tomographies and data from both electron and light microscopes, and create three-dimensional images to interact with. With these reconstructions, IMOD gives researchers the ability to help visualize their samples digitally. The software is able to create collections of images and uses these collections to make models and measurements for further analysis. One tool, the 'slicer', can help view samples at different angles. Some other tools include zooming and panning (called the Zap window), a Model view window of a contour of the sample, an XYZ window that shows the other planes that cut through the point that is being studied, and the Tilt and Tumbler windows that show different projections that can be made. The software can be downloaded and used for free at http://bio3d.colorado.edu. This technology has been used to visualize cytoplasmic membranes, myofibrils, and the trans-Golgi network.
A few years later in 1999, McIntosh's team published a study using cryofixing and electron tomography to create a 3-dimensional model of the Golgi apparatus. Two of the Golgi apparatus's main functions are to modify proteins and to target them to their next destination. For transport within the Golgi, McIntosh's team proposed evidence that it can be done by vesicles in the cell that fuse with different membranes or by microtubules that are constantly forming and shifting around the Golgi. By cryofixing, or rapidly freezing the cells to be studied, McIntosh's team was able to preserve the cells essentially in time before using an electron microscope to visualize them. In this work, the researchers visualized different coatings on the budding parts of the Golgi. They were able to see the difference between clathrin-coated and non-clathrin-coated vesicles. The buds help molecules in the Golgi be transported from the Golgi to their intended area in the cell. In this work, the researchers describe the different cisternae, buds, vesicles, and coatings and the differences between the cis and trans faces of the Golgi. This visualization technique led them to the conclusion that the different cisternae of the Golgi are not interconnected. There are also many vesicles that surround the Golgi, most of which are not coated with clathrin.
2000s In 2002, McIntosh's team continued his earlier interests in "Chromosome-microtubule interactions during mitosis." This review paper explains how spindle microtubules bind to chromosomes during segregation at places called kinetochores and the description of the Kinetochore-Dependent Checkpoint. This point in the cell will block the segregation of chromosomes until all of the chromosomes are properly connected. It also explains the role of microtubule proteins, motor proteins, and the microtubules themselves in the segregation process. Some of the motor proteins mentioned in the article include those associated with the kinetochore at the plus or minus end or those that help with the disassembly of microtubules. Some motor proteins associate with the chromosomes instead of the kinetochores, including chromokinesins, and some work at the spindle poles.
McIntosh also contributed to a work published in 2004 by many scientists in "A standard kinesin nomenclature". In this work, these scientists helped create a naming structure for kinesin proteins, that are involved in transport in the cell along with microtubules. The kinesin proteins were split into fourteen different families, and given different names such as kinesin-1, kinesin-2, etc. This new structure of naming was created so that the existing kinesins can be easily classified as well as classify new kinesin proteins when they are discovered. The authors recommend using protein sequence alignment based homology search to help classify the kinesins. It also makes specifications on what makes a kinesin recognized. Additionally, this paper also gives guidance on how to address kinesins (and their former names, if applicable) in papers.
In 2005, McIntosh and his team published a study that investigated the link between the depolymerization of microtubules and the generation of force, showing how the chemistry of the tubulin dimers can create mechanical force. The researchers attached glass microbeads to tubulin. By using laser tweezers, McIntosh's team was able to observe that the bead would move, typically towards the minus end, as the microtubules depolymerized off of it. In particular, the bending of the protofilaments would cause the tweezers to pick up the force generated. Here, the researchers applied these findings to chromosome segregation and concluded that the microtubule dynamics create the forces needed during mitosis.
In 2006, McIntosh's team used cyroelecton tomography to image axonemes in sea urchin sperm and Chlamydomonas reinhardtii. Axonemes are structures in cilia and flagella consisting of a specific pattern of microtubules. McIntosh's team was particularly interested in the dynein protein. In this paper, the researchers describe how the different subunits of dynein attach to the microtubules and how they might generate force as well.
2010s