Biological Nanomachines

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Transcription:

Biological Nanomachines Yann R Chemla Dept. of Physics, University of Illinois at Urbana Champaign Saturday Physics for Everyone, Sept. 14, 2013

Biophysics at Illinois

Part I: WHAT IS BIOPHYSICS?

Physicists doing biology? Q: Why are physicists interested in biology? A: Physicists want to understand the world around us DNA E. coli cells A cat Simple Complex

What is biophysics? Applying techniques or ideas from physics to biological problems Central problems in biology will become accessible to analysis through basic physical laws. A biophysicist s description of biological phenomena aims to be: Quantitative (mathematical) Simple (captures enough detail but not too much) General (applicable to more than one system) Physics in a New Era NRC(2001) Grand challenges: Applying Physics to Biology Understanding Complex Systems

Part II: MOLECULAR NANOMACHINES

The cellular factory The cell =a nano scale factory of molecular machines DNA genetic blueprint to allcomponents of the cell Proteins carry out cellular tasks Molecular machine Drawing courtesy of M. Spies

Molecular machines Molecular machines move cargo around the cell http://www.xvivo.net/the inner life of the cell/

Molecular machines Molecular machines copy the cell s DNA http://www.dnalc.org/resources/3s/03 mechanism of replication basic.html

Molecular machines Molecular machines propel cells

Molecular distances Strand of hair Bacterial cell (E. coli) > > 01mm 0.1 1 micron = 1/100 X Strand of DNA 1 nanometer = 1/100,000 X Limit of light microscope

Molecular forces Weight of a small apple 1 Newton > Force exerted by a molecular nanomachine 1 piconewton (pn) = 1/1,000,000,000,000 X The apple that fell on Newton s head

Molecular energies Gallon of gasoline Calories in apple 100 MegaJoules 50 Calories = 1/1,000 X ATP: fuel of the cell > > 100 pn nm = 1/100,000,000,000,000, 000,000,000,000 X Adenosine Diphosphate Triphosphate (ADP) (ATP) + Phosphate (P i )

Measurement How do you measure anything? Too small to see Forces & energies too small to detect Traditional biochemistry Test lots of molecules together in a test tube

Bulk biochemistry Individual proteins move stochastically (= at random) This is a problem when doing traditional bulk biochemistry This one went slow Ideally, we want to study these This one one molecule paused at a time This one stopped START FINISH

Measurement How do you measure anything? Too small to see Forces & energies too small to detect Single molecule techniques to the rescue! 280 center 240 200 Photons 160 120 width 250 nm 80 Optical traps 40 0 5 10 15 Y axis Sensitive to individual molecules! 20 20 25 25 15 X Data 0 5 10 Single molecule fluorescence

Part II: SINGLE MOLECULE TECHNIQUES

Optical tweezers Gradient force: F = (p E) = α E 2 Linear spring K ~ 0.1pN/nm measure pn, nm Ashkin et al., Opt. Lett. 11, 288 (1986)

The optical trap......a really expensive LEGO set 19

High resolution traps Optical tweezers can access Ångstrom length scales! 1 Ångstrom = 1/10 nanometer CAGT... Temperature controlled, noise free environment GTCA... 1 DNA basepair = 3.4Å 1Å 59 Loomis

Typical geometries Typical trap experiments involve tethering a single molecule & detecting changes to its length: Surface based (kinesin) Visscher et al. Nature (1999) But tthere are many others...

Example experiment Stretching a DNA hairpin : 3 biotin 3 digoxigenin Hairpin DNA handle DNA handle Streptavidin bead Anti digoxigenin bead Hairpin see also: Woodside et al., PNAS (2006)

Traps in action

Gone fishing 24

DNA Hairpin Transition Force ~15 pn Red = stretching Green = relaxing Hairpin protocol: Woodside et al., PNAS (2006) 25

Part III: DNA MOTORS

DNA Helicases Helicases unwind the strands of DNA 3 5 5 Fuel: ATP ADP + P i Uses ATP fuel to move on one strand of DNA Unwinds double stranded DNA ahead Critical role in replication, recombination and repair 3 Review of helicase: Lohman et al., Nat. Rev. Mol. Cell Biol. 2008 27

Repair helicase Helicases are involved in repairing damaged DNA XPDhelicase atomic structure XPB TFIIH RPA XPD Fan et al., Cell (2008) Nucleotide excision repair

Hairpin Assay Monitor unwinding of a DNA hi hairpin i (under constant force) Δx Change (Δx) in tether extension reveals unwinding activity Qi et al., elife 2013

XPD Stepping Dynamics 1 2 3 4 5 14 AT 11 12 13 TA 6 10 AT GC 9 7 TA 8 CG GC GC DNA sequence affects reversals Time (s) Average step size is 1 bp Backstepping is frequent Step size (bp) Qi et al. elife (2013) Step finding: Kerssemakers et al., Nature (2006)

Helicase mechanism Conclusions 5 3 1. XPD unwinds 1 bp at a time 2. Unwinds & slips DNA repetitively 3. Stalling & backstepping related to DNA sequence New model 1. Helicase unwinds by passive mechanism 2. Repetitive mechanism related to role in repair ATP 3 ADP + P i 5 31

Fishing... in the dark Wouldn t it be nice to see what s on the fishing line? 32

Single molecule fluorescence It is possible to see measure light from distances a single with molecule! pairs of fluorescent molecules FRET 280 240 200 Photons 160 120 80 Spectroscopic ruler 40 0 5 10 15 Y axis 20 25 25 20 15 10 X Data 5 0 Courtesy of Paul Selvin Roy, Hohng & Ha, Nat. Meth. (2008)

Fluorescence & Trap Bead 1 Bead 2 Photo ons/s 1 μm Fluor. Comstock et al., Nat. Meth. (2011) 34

UvrD 2B domain orientation Open ON moving? 2B ~160 rotation Closed Off stalled? 2B Low FRET High FRET UvrD helicase atomic structure Conformation switches function? Crystal structure: Closed at junction (presumed unwinding). Biochemistry and single molecule: Open during motion. Closed at junction stalled. FRET + Trap Jia, Lohman et al., JMB 2011. Park, Ha et al., Cell 2010. Lee and Yang, Cell 2006. Singleton et al., Ann. Rev. Biochem. 2007. 35

Measuring UvrD conformation Dual labeled UvrD DNA Unwo ound (bp) Photo ons (khz) 24 21 18 15 12 9 6-3 03 0.5 1 I Donor 0 I Acceptor FR RET Efficien cy Comstock et al., in preparation 1 Closed 0.5 Open 0 48 49 50 51 52 53 54 55 56 Time (s) 36

Conformation & directionality Velociity (bp/s) Correlation between: conformation (closed/open) & directionality (unwinding/annealing) FRET Comstock et al., in preparation

Strand reversal? Conclusions 1. Closed when unwinding hairpin 2. Open when reannealing Open 3 5 Closed New model 5 1. 2B domain remains anchored to dsdna 2. Motor domains switch strands* Open Closed 3 *Dessinges, et. al., PNAS 2004. 38

Part IV: OUTLOOK

Biophysicists wear many hats... Molecular biology Nature of research Experimentalist build instruments Biologist develop the biological system Theorist model the data Optics Data collection and analysis

Take home message Hey You put physics into my biology! No You put biology into my physics! BIOLOGY PHYSICS Quantification of Biological Systems TAKE HOME MESSAGE These advances present new directions for BOTH biology and physics. 41

Acknowledgements XPD Helicase stepping Zhi Qi Maria Spies & Robert Pugh (Univ. of Iowa) UvrD trap & fluorescence: Matt Comstock* Kevin Whitley Taekjip Ha (Univ. of Illinois) Tim Lohman & Haifeng Jia (Washington Univ.) Now at: Columbia Univ. * Michigan State Univ. Funding: