Lulu Qian

Last updated
Lulu Qian
Born
Alma mater Nanjing Railway University
Shanghai Jiao Tong University
Scientific career
Institutions California Institute of Technology
Academic advisors Erik Winfree

Lulu Qian is a Chinese-American biochemist who is a professor at the California Institute of Technology. Her research uses DNA-like molecules to build artificial machines.

Contents

Early life and education

Qian is from China. She completed her bachelor's degree in biomedical engineering at Southeast University in Nanjing. [1] Qian moved to Shanghai for her doctoral research, where she worked at Shanghai Jiao Tong University on biochemistry. [2] She then moved to the California Institute of Technology as a postdoctoral fellow. [3] At Caltech, she worked alongside Erik Winfree on biochemical circuits. She used a reversible strand displacement process to create a simple DNA-based building block for a biochemical logic circuit. [4]

Research and career

Qian joined the faculty at Caltech in 2013. She was promoted to professor in 2019. [5] Her research considers molecular robotics and the self-assembly of nanostructures from DNA. These molecular robots can explore biologically relevant surfaces at the nanoscale, picking up molecules and transporting them to specific locations. [6] In 2011, she created the world's largest DNA circuit, which included over seventy DNA molecules. [7]

Qian has also created complex DNA origami. [8] She created two-dimensional images from DNA origami tiles. [8] She used DNA to create an artificial neural network. [9] The network consisted of a DNA gate architecture that can be scaled up into multi-layer circuits. [9] [10]

Awards and honors

Selected publications

Related Research Articles

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<span class="mw-page-title-main">John Hopfield</span> American scientist (born 1933)

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<span class="mw-page-title-main">DNA origami</span> Folding of DNA to create two- and three-dimensional shapes at the nanoscale

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<span class="mw-page-title-main">Nucleic acid secondary structure</span>

Nucleic acid secondary structure is the basepairing interactions within a single nucleic acid polymer or between two polymers. It can be represented as a list of bases which are paired in a nucleic acid molecule. The secondary structures of biological DNAs and RNAs tend to be different: biological DNA mostly exists as fully base paired double helices, while biological RNA is single stranded and often forms complex and intricate base-pairing interactions due to its increased ability to form hydrogen bonds stemming from the extra hydroxyl group in the ribose sugar.

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<span class="mw-page-title-main">Barbara Wold</span> Professor of Molecular Biology

Barbara J. Wold is the Bren Professor of Molecular Biology, the principal investigator of the Wold Lab at the California Institute of Technology (Caltech) and the principal investigator of the Functional Genomics Resource Center at the Beckman Institute at Caltech. Wold was director of the Beckman Institute at Caltech from 2001 to 2011.

<span class="mw-page-title-main">Toehold mediated strand displacement</span>

Toehold mediated strand displacement (TMSD) is an enzyme-free molecular tool to exchange one strand of DNA or RNA (output) with another strand (input). It is based on the hybridization of two complementary strands of DNA or RNA via Watson-Crick base pairing (A-T/U and C-G) and makes use of a process called branch migration. Although branch migration has been known to the scientific community since the 1970s, TMSD has not been introduced to the field of DNA nanotechnology until 2000 when Yurke et al. was the first who took advantage of TMSD. He used the technique to open and close a set of DNA tweezers made of two DNA helices using an auxiliary strand of DNA as fuel. Since its first use, the technique has been modified for the construction of autonomous molecular motors, catalytic amplifiers, reprogrammable DNA nanostructures and molecular logic gates. It has also been used in conjunction with RNA for the production of kinetically-controlled ribosensors. TMSD starts with a double-stranded DNA complex composed of the original strand and the protector strand. The original strand has an overhanging region the so-called “toehold” which is complementary to a third strand of DNA referred to as the “invading strand”. The invading strand is a sequence of single-stranded DNA (ssDNA) which is complementary to the original strand. The toehold regions initiate the process of TMSD by allowing the complementary invading strand to hybridize with the original strand, creating a DNA complex composed of three strands of DNA. This initial endothermic step is rate limiting and can be tuned by varying the strength (length and sequence composition e.g. G-C or A-T rich strands) of the toehold region. The ability to tune the rate of strand displacement over a range of 6 orders of magnitude generates the backbone of this technique and allows the kinetic control of DNA or RNA devices. After the binding of the invading strand and the original strand occurred, branch migration of the invading domain then allows the displacement of the initial hybridized strand (protector strand). The protector strand can possess its own unique toehold and can, therefore, turn into an invading strand itself, starting a strand-displacement cascade. The whole process is energetically favored and although a reverse reaction can occur its rate is up to 6 orders of magnitude slower. Additional control over the system of toehold mediated strand displacement can be introduced by toehold sequestering.

TectoRNAs are modular RNA units able to self-assemble into larger nanostructures in a programmable fashion. They are generated by rational design through an approach called RNA architectonics, which make use of RNA structural modules identified in natural RNA molecules to form pre-defined 3D structures spontaneously.

References

  1. "Lulu Qian | Caltech Directory". directory.caltech.edu. Retrieved 2023-03-05.
  2. "Introducing ISNSCE Vice President Lulu Qian". ISNSCE. 2021-12-11. Retrieved 2023-03-05.
  3. "Programming DNA for Molecular Robots: An Interview with Lulu Qian – Pasadena Now". www.pasadenanow.com. Retrieved 2023-03-05.
  4. Qian, Lulu; Winfree, Erik (2011-06-03). "Scaling Up Digital Circuit Computation with DNA Strand Displacement Cascades". Science. 332 (6034): 1196–1201. Bibcode:2011Sci...332.1196Q. doi:10.1126/science.1200520. ISSN   0036-8075. PMID   21636773. S2CID   10053541.
  5. "Lulu Qian's CV" (PDF).
  6. Major, Mario L. (2017-09-16). "Scientists Build DNA Robots That Could One Day Deliver Medicine Inside Your Body". interestingengineering.com. Retrieved 2023-03-04.
  7. "Caltech researchers build largest biochemical circuit out of small synthetic DNA molecules". EurekAlert!. Retrieved 2023-03-04.
  8. 1 2 Andy Extance2017-12-07T14:30:00+00:00. "DNA origami makes it big". Chemistry World. Retrieved 2023-03-04.{{cite web}}: CS1 maint: numeric names: authors list (link)
  9. 1 2 Qian, Lulu; Winfree, Erik; Bruck, Jehoshua (July 2011). "Neural network computation with DNA strand displacement cascades". Nature. 475 (7356): 368–372. doi:10.1038/nature10262. ISSN   1476-4687. PMID   21776082. S2CID   1735584.
  10. Mehar, Pranjal (2018-07-10). "Scientists created AI from DNA". Tech Explorist. Retrieved 2023-03-04.
  11. "Foresight Institute Awards 2019 Feynman Prizes in Nanotechnology to Qian, Galli; awards presented by Nobelist, Sir Fraser Stoddart". PRWeb. Retrieved 2023-03-04.
  12. "Two Professors Receive Caltech's Highest Honors for Teaching and Mentorship". California Institute of Technology. 2023-02-21. Retrieved 2023-03-04.