Garth L. Nicolson

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Garth L. Nicolson
Born (1943-10-01) October 1, 1943 (age 80)
Alma mater University of California, Los Angeles (BS)
University of California, San Diego (PhD)
Known for Fluid Mosaic Model
Gulf War syndrome
SpouseNancy L. Nicolson
Scientific career
Fields Biochemistry
Cell biology
Institutions Salk Institute for Biological Studies
University of California, Irvine
University of Texas
Texas A&M University
The Institute for Molecular Medicine
Website www.immed.org

Garth L. Nicolson (born October 1, 1943) [1] is an American biochemist who made a landmark scientific model for cell membrane, known as the fluid mosaic model. He is the founder of The Institute for Molecular Medicine at California, and he serves as the president, chief scientific officer and emeritus professor of molecular pathology. He is also a conjoint professor in the Faculty of Science and Technology, University of Newcastle, Australia.

Contents

During the outbreak of the Gulf War syndrome, he was the leading authority on the study of the cause, treatment and prevention of the disease. He was appointed chairman of the Medical-Scientific Panel for the Persian Gulf War Veterans Conference. [2] On suspicion of the bacterium that caused the disease as a product of biological warfare, he made extensive scientific investigations and served as authority to the United States House of Representatives. [3] For his service he was conferred honorary Colonel of the US Army Special Forces and honorary US Navy SEAL. [4]

With S.J. Singer, Nicolson published a paper titled "The Fluid Mosaic Model of the Structure of Cell Membranes" in 1972, [5] which is now regarded as a classic paper in cell biology. [6] [7] [8]

With over 600 scientific papers, the majority of Nicolson's research is in cancer biology and cellular properties related to aging.

Biography

Nicolson was born in Los Angeles, California. He graduated from the University of California, Los Angeles in 1965 with a major in chemistry. He joined research in biochemistry at the University of California, San Diego, from where he earned his PhD in 1970. He was a USPHS Predoctoral Fellow from 1967 to 1970. During 1970–1971 he worked as senior research associate in the Armand Hammer Cancer Centre of the Cancer Council Laboratory at the Salk Institute for Biological Studies, La Jolla. He became head of the Cancer Council Laboratory, as well as director of Electron Microscopy Laboratory in 1972. In 1974 he took the chair of the department of cancer biology, the post he held till 1976. In 1975 he was appointed professor in the Department of Developmental and Cell Biology at the University of California, Irvine. In 1978 he additionally became professor in the department of physiology and biophysics at the College of Medicine, University of California, Irvine. In 1980 he was conferred the post Florence M. Thomas Professor of Cancer Research at the University of Texas M. D. Anderson Cancer Center, Houston, where he worked for seven years. Between 1980 and 1996 he was also professor at the Graduate School of Biomedical Sciences, the University of Texas Health Science Center; as well as David Bruton Jr. Chair in Cancer Research, professor and chairman of tumor biology at The University of Texas M. D. Anderson Cancer Center. He was also professor in the department of pathology and laboratory medicine at the University of Texas Medical School from 1982 to 1998. During 1981–1998 he was adjunct professor in the department of pathology at the school of veterinary medicine, Texas A & M University. From 1989 to 1999 he was professor in the department of internal medicine at the University of Texas Medical School. [1] In 1996 he founded The Institute for Molecular Medicine at Huntington Beach in 1996. [9] He became its president, chief scientific officer and research professor of molecular pathology. He also serves as professor of integrative medicine at Capitol University of Integrative Medicine. Since 2003 he is also the conjoint professor in the faculty of science and technology at the University of Newcastle, Australia. [2] [3] He is a founding editor of the editorial board of the Cancer and Metastasis Reviews. [10]

Contributions

Fluid mosaic model of cell membrane

While working as research associate at the Salk Institute for Biological Studies, Nicolson collaborated with S.J. Singer at the University of California, San Diego. They made a seminal model for the structure of cell membranes, which they named the Fluid Mosaic Model, and published in a 12-page paper in the February 18, 1972, issue of Science . [5] It was the first model in cell biology to be based on thermodynamics properties. Earlier descriptions of the cell membrane had serious inconsistencies with observed properties of the lipid bilayer. [11] According to the Fluid Mosaic Model, in contrast to other models, the cell membrane is composed of a single lipid bilayer which is associated with two groups of proteins. Peripheral proteins are located on the surface, while integral proteins are embedded the lipid layer. The proteins are highly varied, thus, creating a mosaic pattern. Majority of the membrane is composed of phospholipids, which exhibit fluidity like oil. The phospholids are not just stationary, but are able to move, and the proteins can move in the fluid lipid layer. These properties give the membrane flexibility. [12] The model turned out to be the foundation of modern understanding of cell membrane structure and functions. Although its basic assumptions are still true, the dynamic nature has been underestimated, and more information have been incorporated with new discoveries. [6] [7] [8] [13] [14] [15] [16] [17]

Gulf War syndrome and controversy

After the Gulf War of 1990–1991, a number of war veterans suffered from similar illness, popularly dubbed Gulf War syndrome. [18] They indicated symptoms like chronic fatigue, headaches, memory loss, muscle pain, nausea, gastrointestinal problems, joint pain, lymph node pain, increased chemical sensitivities and other signs and symptoms. Nicolson became one of the leading experts in the investigation of the cause and cure of the disease. [19] Initially the US government disregarded the illnesses as the aftermath of the Gulf War, such as exposure to biological or chemical warfare. Nicolson and his wife Nancy became the main voice to raise the problem. [20] They identified the causal pathogen as Mycoplasma fermentans , which was a different strain from the natural pathogen, raising the possibility that it was man-made biological weapon. [21] They successfully treated patients with multiple courses of specific antibiotics, such as doxycycline, ciprofloxacin, azithromycin, clarithromycin or minocycline. [22] Nicolson's "Written Testimony" to the US Senate in 1998 states that: "We consider it quite likely that many of the Desert Storm veterans suffering from the GWI signs and symptoms may have been exposed to chemical/biological toxins (exogenous or endogenous sources of these agents) containing slowly proliferating microorganisms ( Mycoplasma , Brucella , Coxiella , etc.), and such infections, although not usually fatal, can produce various chronic signs and symptoms long after exposure." [23] While other researchers found negative results for Mycoplasma infection, [24] [25] Nicolson's team found definite high prevalence of Mycoplasma infections. [26]

Awards and recognitions

Related Research Articles

<span class="mw-page-title-main">Biological membrane</span> Enclosing or separating membrane in organisms acting as selective semi-permeable barrier

A biological membrane, biomembrane or cell membrane is a selectively permeable membrane that separates the interior of a cell from the external environment or creates intracellular compartments by serving as a boundary between one part of the cell and another. Biological membranes, in the form of eukaryotic cell membranes, consist of a phospholipid bilayer with embedded, integral and peripheral proteins used in communication and transportation of chemicals and ions. The bulk of lipids in a cell membrane provides a fluid matrix for proteins to rotate and laterally diffuse for physiological functioning. Proteins are adapted to high membrane fluidity environment of the lipid bilayer with the presence of an annular lipid shell, consisting of lipid molecules bound tightly to the surface of integral membrane proteins. The cell membranes are different from the isolating tissues formed by layers of cells, such as mucous membranes, basement membranes, and serous membranes.

<span class="mw-page-title-main">Phospholipid</span> Class of lipids

Phospholipids are a class of lipids whose molecule has a hydrophilic "head" containing a phosphate group and two hydrophobic "tails" derived from fatty acids, joined by an alcohol residue. Marine phospholipids typically have omega-3 fatty acids EPA and DHA integrated as part of the phospholipid molecule. The phosphate group can be modified with simple organic molecules such as choline, ethanolamine or serine.

<span class="mw-page-title-main">Fluid mosaic model</span> Describe the fluid mosaic model of plasma membrane

The fluid mosaic model explains various characteristics regarding the structure of functional cell membranes. According to this biological model, there is a lipid bilayer in which protein molecules are embedded. The phospholipid bilayer gives fluidity and elasticity to the membrane. Small amounts of carbohydrates are also found in the cell membrane. The biological model, which was devised by Seymour Jonathan Singer and Garth L. Nicolson in 1972, describes the cell membrane as a two-dimensional liquid that restricts the lateral diffusion of membrane components. Such domains are defined by the existence of regions within the membrane with special lipid and protein cocoon that promote the formation of lipid rafts or protein and glycoprotein complexes. Another way to define membrane domains is the association of the lipid membrane with the cytoskeleton filaments and the extracellular matrix through membrane proteins. The current model describes important features relevant to many cellular processes, including: cell-cell signaling, apoptosis, cell division, membrane budding, and cell fusion. The fluid mosaic model is the most acceptable model of the plasma membrane. In this definition of the cell membrane, its main function is to act as a barrier between the contents inside the cell and the extracellular environment.

Mycoplasma pneumoniae is a very small cell wall-less bacterium in the class Mollicutes. It is a human pathogen that causes the disease mycoplasma pneumonia, a form of atypical bacterial pneumonia related to cold agglutinin disease. M. pneumoniae is characterized by the absence of a peptidoglycan cell wall and resulting resistance to many antibacterial agents. The persistence of M. pneumoniae infections even after treatment is associated with its ability to mimic host cell surface composition.

<span class="mw-page-title-main">Lipid raft</span> Combination in the membranes of cells

The plasma membranes of cells contain combinations of glycosphingolipids, cholesterol and protein receptors organised in glycolipoprotein lipid microdomains termed lipid rafts. Their existence in cellular membranes remains controversial. Indeed, Kervin and Overduin imply that lipid rafts are misconstrued protein islands, which they propose form through a proteolipid code. Nonetheless, it has been proposed that they are specialized membrane microdomains which compartmentalize cellular processes by serving as organising centers for the assembly of signaling molecules, allowing a closer interaction of protein receptors and their effectors to promote kinetically favorable interactions necessary for the signal transduction. Lipid rafts influence membrane fluidity and membrane protein trafficking, thereby regulating neurotransmission and receptor trafficking. Lipid rafts are more ordered and tightly packed than the surrounding bilayer, but float freely within the membrane bilayer. Although more common in the cell membrane, lipid rafts have also been reported in other parts of the cell, such as the Golgi apparatus and lysosomes.

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References

  1. 1 2 "Curriculum Vitae GARTH L. NICOLSON". The Institute for Molecular Medicine. February 20, 2010. Archived from the original on August 8, 2021. Retrieved August 6, 2014.
  2. 1 2 "Professor Emeritus Garth L. Nicolson" (PDF). The Institute for Molecular Medicine. Archived from the original (PDF) on January 23, 2019. Retrieved August 7, 2014.
  3. 1 2 Nicolson, Garth L; Nicolson, Nancy L. "About the authors". Project Day Lily. Archived from the original on August 12, 2014. Retrieved August 6, 2014.
  4. "IMM – Faculty and Associate Faculty". The Institute for Molecular Medicine. Retrieved August 7, 2014.
  5. 1 2 Singer, S. J.; Nicolson, G. L. (1972). "The Fluid Mosaic Model of the Structure of Cell Membranes". Science. 175 (4023): 720–731. Bibcode:1972Sci...175..720S. doi:10.1126/science.175.4023.720. JSTOR   1733071. PMID   4333397. S2CID   83851531.
  6. 1 2 Cherry, Richard (1991). New Techniques of Optical Microscopy and Microspectroscopy. Boca Raton, Florida: CRC Press, Inc. p. 199. ISBN   978-0-8493-7117-2. ISSN   0265-4377.{{cite book}}: |journal= ignored (help)
  7. 1 2 Luckey, Mary (2014). Membrane Structural Biology: With Biochemical and Biophysical Foundations (2 ed.). Cambridge (UK): Cambridge University Press. p. 6. ISBN   978-1-107-72933-9.
  8. 1 2 Jacobson, K; Sheets, E.; Simson, R (1995). "Revisiting the fluid mosaic model of membranes". Science. 268 (5216): 1441–1442. Bibcode:1995Sci...268.1441J. doi:10.1126/science.7770769. PMID   7770769.
  9. "Garth Nicolson Prof". iHealthTube. February 7, 2013. Retrieved August 6, 2014.
  10. "Cancer and Metastasis Reviews".
  11. Martin, Laura. "The Fluid Mosaic Model of the Cell Membrane – The Mosaic". oepnstax cnx. Retrieved August 7, 2014.
  12. Ash, Michael (August 28, 2012). "A Special Note from Garth Nicolson PhD Why Lipid Replacement Therapy(LRT®) is Key to our Health". Clinical Education. Nutri-Link Ltd. Retrieved August 7, 2014.
  13. Wiśniewska, A; Draus, J; Subczynski, WK (2003). "Is a fluid-mosaic model of biological membranes fully relevant? Studies on lipid organization in model and biological membranes". Cellular & Molecular Biology Letters. 8 (1): 147–159. PMID   12655369.
  14. Engelman, Donald M. (2005). "Membranes are more mosaic than fluid". Nature. 438 (7068): 578–580. Bibcode:2005Natur.438..578E. doi: 10.1038/nature04394 . PMID   16319876. S2CID   4416823.
  15. Kusumi, Akihiro; Fujiwara, Takahiro K.; Chadda, Rahul; Xie, Min; Tsunoyama, Taka A.; Kalay, Ziya; Kasai, Rinshi S.; Suzuki, Kenichi G.N. (2012). "Dynamic organizing principles of the plasma membrane that regulate signal transduction: commemorating the fortieth anniversary of Singer and Nicolson's fluid-mosaic model". Annual Review of Cell and Developmental Biology. 28 (1): 215–250. doi:10.1146/annurev-cellbio-100809-151736. PMID   22905956.
  16. Nicolson, Garth (2013). "Update of the 1972 Singer-Nicolson Fluid-Mosaic Model of Membrane Structure". Discoveries. 1 (1): e3. doi: 10.15190/d.2013.3 . PMC   7159824 . PMID   32309537.
  17. Nicolson, Garth L. (2014). "The Fluid—Mosaic Model of Membrane Structure: Still relevant to understanding the structure, function and dynamics of biological membranes after more than 40 years". Biochimica et Biophysica Acta (BBA) - Biomembranes. 1838 (6): 1451–1466. doi: 10.1016/j.bbamem.2013.10.019 . PMID   24189436.
  18. Nicolson, GL; Nicolson, NL (1997). "The eight myths of Operation 'Desert Storm' and Gulf War syndrome". Medicine, Conflict, and Survival. 13 (2): 140–6. doi:10.1080/13623699708409329. PMID   9178600.
  19. Nicolson, GL; Bruton DM, Jr; Nicolson, NL (1996). "Chronic fatigue illness and Operation Desert Storm". Journal of Occupational and Environmental Medicine. 38 (1): 14–6. doi: 10.1097/00043764-199601000-00003 . PMID   8871324.
  20. Nicolson, GL; Nicolson, NL (1997). "The eight myths of Operation 'Desert Storm' and Gulf War syndrome". Medicine, Conflict, and Survival. 13 (2): 140–146. doi:10.1080/13623699708409329. PMID   9178600.
  21. Blair, Mike (July 3, 1995). "The Government Is Lying To You -- And Ill Veterans -- About Gulf War Syndrome". The Spotlight. Archived from the original on February 24, 2016. Retrieved August 9, 2014.
  22. Nicolson, G (2001). "Continuing research into Gulf War illness". Science. 292 (5518): 853b–853. doi:10.1126/science.292.5518.853b. PMID   11341275. S2CID   19886150.
  23. Nicolson, Garth L (November 19, 1998). "WRITTEN TESTIMONY OF Dr. Garth L. Nicolson Special Oversight Board for Department of Defense Investigations of Gulf War Chemical and Biological Incidents". U. S. Senate Hart Office Building SH-216. Retrieved August 9, 2014.
  24. Gray, GC; Kaiser, KS; Hawksworth, AW; Watson, HL (1999). "No serologic evidence of an association found between Gulf War service and Mycoplasma fermentans infection". The American Journal of Tropical Medicine and Hygiene. 60 (5): 752–7. doi:10.4269/ajtmh.1999.60.752. PMID   10344648. S2CID   32534013.
  25. Lo, SC; Levin, L; Ribas, J; Chung, R; Wang, RY; Wear, D; Shih, JW (2000). "Lack of serological evidence for Mycoplasma fermentans infection in army Gulf War veterans: a large scale case-control study". Epidemiology and Infection. 125 (3): 609–16. doi:10.1017/s0950268800004891. PMC   2869645 . PMID   11218212.
  26. Nicolson, Garth L.; Nasralla, Marwan Y.; Haier, Joerg; Pomfret, John (2002). "High frequency of systemic mycoplasmal infections in Gulf War veterans and civilians with Amyotrophic Lateral Sclerosis (ALS)". Journal of Clinical Neuroscience. 9 (5): 525–529. doi:10.1054/jocn.2001.1075. PMID   12383408. S2CID   24870742.