This article is an autobiography or has been extensively edited by the subject or by someone connected to the subject.(April 2019) |
David W. Deamer | |
---|---|
Born | Santa Monica, CA | April 21, 1939
Nationality | American |
Occupation | Biologist |
Awards | Guggenheim Fellow, 1985 |
Academic background | |
Education | Duke University (B.Sc. 1961) Ohio State University (Ph.D. 1965) |
Alma mater | Ohio State University |
Thesis | The effect of alkaline earth ions on fatty acid and phospholipid monolayers (1965) |
Doctoral advisor | David Cornwell |
Academic work | |
Discipline | Biophysicist |
Institutions | University of California,Santa Cruz |
Notable ideas | nanopore sequencing |
David Wilson Deamer (born April 21,1939) is an American biologist and Research Professor of Biomolecular Engineering at the University of California,Santa Cruz. Deamer has made significant contributions to the field of membrane biophysics. His work led to a novel method of DNA sequencing and a more complete understanding of the role of membranes in the origin of life.
He was awarded a Guggenheim Fellowship in 1985,which supported research at the Australian National University in Canberra to investigate organic compounds in the Murchison meteorite. He served as the president of the International Society for the Study of the Origin of Life from 2013 to 2014.[ citation needed ]
Deamer's father,also David,worked at Douglas Aircraft in Santa Monica,California,during and after World War II while his mother Zena cared for Deamer and his two brothers,Richard and John. In 1952,the family moved to Ohio,where the three brothers attended Westerville High School. In 1957,Deamer submitted his research on self-organizing protozoa to the Westinghouse Science Talent Search and was among the 40 winners who were invited to Washington DC that year. He was awarded a full scholarship to Duke University,where he completed a bachelor's degree in chemistry in 1961. [1]
As a young professor at UC Davis,Deamer continued to work with electron microscopy,revealing for the first time particles related to functional ATPase enzymes within the membranes of sarcoplasmic reticulum. [2] After spending sabbaticals in England at the University of Bristol in 1971 and with Alec Bangham in 1975,Deamer became interested in liposomes. Conversations with Bangham inspired his research on the role of membranes in the origin of life,and in 1985 Deamer demonstrated that the Murchison carbonaceous meteorite contained lipid-like compounds that could assemble into membranous vesicles. [3] Deamer described the significance of self-assembly processes in his 2011 book First Life. [4] In collaborative work with Mark Akeson,a post-doctoral student at the time,the two established methods for monitoring proton permeation through ion channels such as gramicidin. [5] In 1989,while returning from a scientific meeting in Oregon,Deamer conceived that it might be possible to sequence single molecules of DNA by using an imposed voltage to pull them individually through a nanoscopic channel. The DNA sequence could be distinguished by the specific modulating effect of the four bases on the ionic current through the channel. In 1993,he and Dan Branton initiated a research collaboration with John Kasianowitz at NIST to explore this possibility with the hemolysin channel,and in 1996 published the first paper demonstrating that nanopore sequencing may be feasible. [6] George Church at Harvard had independently proposed a similar idea,and Church,Branton and Deamer decided to initiate a patent application which was awarded in 1998. [7] Mark Akeson joined the research effort in 1997,and in 1999 published a paper showing that the hemolysin channel,now referred to as a nanopore,could distinguish between purine and pyrimidine bases in single RNA molecules. [8] In 2007,Oxford Nanopore Technologies (ONT) licensed the patents describing the technology [9] and in 2014 released the MinION nanopore sequencing device to selected researchers. The first publications appeared in 2015,one of which used the MinION to sequence E. coli DNA with 99.4% accuracy relative to the established 5.4 million base pair genome. [10] Despite earlier skepticism,nanopore sequencing is now accepted as a viable third generation sequencing method. [11] [12] [13] [14]
Deamer is also the co-author with science writer Wallace Kaufman of a sci-fi novel,The Hunt for FOXP5:A Genomic Mystery Novel (Springer,2016). Through characters in American universities and Kazakhstani science and politics the authors explore the ethical complexity of editing human genes.
A DNA sequencer is a scientific instrument used to automate the DNA sequencing process. Given a sample of DNA,a DNA sequencer is used to determine the order of the four bases:G (guanine),C (cytosine),A (adenine) and T (thymine). This is then reported as a text string,called a read. Some DNA sequencers can be also considered optical instruments as they analyze light signals originating from fluorochromes attached to nucleotides.
A transmembrane protein (TP) is a type of integral membrane protein that spans the entirety of the cell membrane. Many transmembrane proteins function as gateways to permit the transport of specific substances across the membrane. They frequently undergo significant conformational changes to move a substance through the membrane. They are usually highly hydrophobic and aggregate and precipitate in water. They require detergents or nonpolar solvents for extraction,although some of them (beta-barrels) can be also extracted using denaturing agents.
A nanopore is a pore of nanometer size. It may,for example,be created by a pore-forming protein or as a hole in synthetic materials such as silicon or graphene.
Nanopore sequencing is a third generation approach used in the sequencing of biopolymers —specifically,polynucleotides in the form of DNA or RNA.
DNA sequencing is the process of determining the nucleic acid sequence –the order of nucleotides in DNA. It includes any method or technology that is used to determine the order of the four bases:adenine,guanine,cytosine,and thymine. The advent of rapid DNA sequencing methods has greatly accelerated biological and medical research and discovery.
In the mitochondrion,the matrix is the space within the inner membrane. The word "matrix" stems from the fact that this space is viscous,compared to the relatively aqueous cytoplasm. The mitochondrial matrix contains the mitochondrial DNA,ribosomes,soluble enzymes,small organic molecules,nucleotide cofactors,and inorganic ions.[1] The enzymes in the matrix facilitate reactions responsible for the production of ATP,such as the citric acid cycle,oxidative phosphorylation,oxidation of pyruvate,and the beta oxidation of fatty acids.
Gramicidin,also called gramicidin D,is a mix of ionophoric antibiotics,gramicidin A,B and C,which make up about 80%,5%,and 15% of the mix,respectively. Each has 2 isoforms,so the mix has 6 different types of gramicidin molecules. They can be extracted from Brevibacillus brevis soil bacteria. Gramicidins are linear peptides with 15 amino acids. This is in contrast to unrelated gramicidin S,which is a cyclic peptide.
Alpha-toxin,also known as alpha-hemolysin (Hla),is the major cytotoxic agent released by bacterium Staphylococcus aureus and the first identified member of the pore forming beta-barrel toxin family. This toxin consists mostly of beta-sheets (68%) with only about 10% alpha-helices. The hly gene on the S. aureus chromosome encodes the 293 residue protein monomer,which forms heptameric units on the cellular membrane to form a complete beta-barrel pore. This structure allows the toxin to perform its major function,development of pores in the cellular membrane,eventually causing cell death.
The ATP5MC1 gene is one of three human paralogs that encode membrane subunit c of the mitochondrial ATP synthase.
John Hagan Pryce Bayley FRS FLSW is a British scientist,who holds the position of Professor of Chemical Biology at the University of Oxford.
DNA nanotechnology is the design and manufacture of artificial nucleic acid structures for technological uses. In this field,nucleic acids are used as non-biological engineering materials for nanotechnology rather than as the carriers of genetic information in living cells. Researchers in the field have created static structures such as two- and three-dimensional crystal lattices,nanotubes,polyhedra,and arbitrary shapes,and functional devices such as molecular machines and DNA computers. The field is beginning to be used as a tool to solve basic science problems in structural biology and biophysics,including applications in X-ray crystallography and nuclear magnetic resonance spectroscopy of proteins to determine structures. Potential applications in molecular scale electronics and nanomedicine are also being investigated.
Synthetic ion channels are de novo chemical compounds that insert into lipid bilayers,form pores,and allow ions to flow from one side to the other. They are man-made analogues of natural ion channels,and are thus also known as artificial ion channels. Compared to biological channels,they usually allow fluxes of similar magnitude but are
A two-state trajectory is a dynamical signal that fluctuates between two distinct values:ON and OFF,open and closed,,etc. Mathematically,the signal has,for every either the value or .
Magnetic sequencing is a single-molecule sequencing method in development. A DNA hairpin,containing the sequence of interest,is bound between a magnetic bead and a glass surface. A magnetic field is applied to stretch the hairpin open into single strands,and the hairpin refolds after decreasing of the magnetic field. The hairpin length can be determined by direct imaging of the diffraction rings of the magnetic beads using a simple microscope. The DNA sequences are determined by measuring the changes in the hairpin length following successful hybridization of complementary nucleotides.
Oxford Nanopore Technologies plc is a UK-based company which develops and sells nanopore sequencing products for the direct,electronic analysis of single molecules.
Oleg Vladimirovich Krasilnikov was a Soviet-born biophysicist who lived and worked in Uzbekistan and Brazil. His father,Vladimir Sergeyevich Krasilnikov,was a mining engineer who worked in the coal mines of Kyrgyzstan. His mother,Ekatherine Yakovlevna Krasilnikova,was an economist.
Third-generation sequencing is a class of DNA sequencing methods currently under active development.
Cynthia J. Burrows is an American chemist,currently a distinguished professor in the department of chemistry at the University of Utah,where she is also the Thatcher Presidential Endowed Chair of Biological Chemistry. Burrows was the Senior Editor of the Journal of Organic Chemistry (2001-2013) and became Editor-in-Chief of Accounts of Chemical Research in 2014.,,
Aleksandra Radenovic is a Swiss and Croatian biophysicist. Her research focuses on the development of experimental tools to study single-molecule biophysics. She is a professor of biological engineering at the École Polytechnique Fédérale de Lausanne (EPFL) and head of the Laboratory of Nanoscale Biology.
Jens Horst Gundlach is a German physicist.