scholarly article | Q13442814 |
P2093 | author name string | Yongli Zhang | |
P2860 | cites work | Modification of a hydrophobic layer by a point mutation in syntaxin 1A regulates the rate of synaptic vesicle fusion | Q21563602 |
Mechanical unzipping and rezipping of a single SNARE complex reveals hysteresis as a force-generating mechanism | Q22061733 | ||
Direct observation of base-pair stepping by RNA polymerase | Q24540192 | ||
Differential detection of dual traps improves the spatial resolution of optical tweezers | Q24548494 | ||
Alpha-synuclein promotes SNARE-complex assembly in vivo and in vitro | Q24629968 | ||
Membrane fusion: grappling with SNARE and SM proteins | Q24633113 | ||
Conserved structural features of the synaptic fusion complex: SNARE proteins reclassified as Q- and R-SNAREs | Q24656954 | ||
Neurotransmitter release: the last millisecond in the life of a synaptic vesicle | Q26269845 | ||
Lipid-anchored SNAREs lacking transmembrane regions fully support membrane fusion during neurotransmitter release | Q26269847 | ||
SNARE zippering | Q26751424 | ||
Molecular machines governing exocytosis of synaptic vesicles | Q26849286 | ||
A Chemical Controller of SNARE-Driven Membrane Fusion That Primes Vesicles for Ca(2+)-Triggered Millisecond Exocytosis | Q27336160 | ||
Helical extension of the neuronal SNARE complex into the membrane | Q27646399 | ||
Dynamic structure of lipid-bound synaptobrevin suggests a nucleation-propagation mechanism for trans-SNARE complex formation | Q27658206 | ||
A switch between two-, three-, and four-stranded coiled coils in GCN4 leucine zipper mutants | Q27731470 | ||
Crystal structure of a SNARE complex involved in synaptic exocytosis at 2.4 A resolution | Q27765619 | ||
SNAP receptors implicated in vesicle targeting and fusion | Q28131653 | ||
SNAREpins: minimal machinery for membrane fusion | Q28131697 | ||
Mechanical processes in biochemistry | Q28266209 | ||
Structure and conformational changes in NSF and its membrane receptor complexes visualized by quick-freeze/deep-etch electron microscopy | Q28581498 | ||
Synaptotagmin-mediated bending of the target membrane is a critical step in Ca(2+)-regulated fusion | Q28584744 | ||
SNAREs--engines for membrane fusion | Q29547230 | ||
Stretching DNA | Q30040484 | ||
High-resolution optical tweezers for single-molecule manipulation | Q30449157 | ||
Multiple intermediates in SNARE-induced membrane fusion | Q30478481 | ||
In vitro system capable of differentiating fast Ca2+-triggered content mixing from lipid exchange for mechanistic studies of neurotransmitter release | Q30502775 | ||
Interactions between synaptic vesicle fusion proteins explored by atomic force microscopy | Q30960921 | ||
Single-molecule studies of SNARE complex assembly reveal parallel and antiparallel configurations | Q31031114 | ||
Single molecule mechanical probing of the SNARE protein interactions | Q33241577 | ||
Interference model for back-focal-plane displacement detection in optical tweezers. | Q33310600 | ||
Pulling force generated by interacting SNAREs facilitates membrane hemifusion. | Q33519916 | ||
Single Molecule Measurements of Interaction Free Energies Between the Proteins Within Binary and Ternary SNARE Complexes | Q33526994 | ||
Purification of an N-ethylmaleimide-sensitive protein catalyzing vesicular transport | Q33658648 | ||
How could SNARE proteins open a fusion pore? | Q33918609 | ||
Common intermediates and kinetics, but different energetics, in the assembly of SNARE proteins | Q34196813 | ||
Role of the synaptobrevin C terminus in fusion pore formation | Q34276398 | ||
Single reconstituted neuronal SNARE complexes zipper in three distinct stages | Q34294781 | ||
Transmembrane segments of syntaxin line the fusion pore of Ca2+-triggered exocytosis. | Q34305380 | ||
The membrane fusion enigma: SNAREs, Sec1/Munc18 proteins, and their accomplices--guilty as charged? | Q34305507 | ||
Timing of neurotransmission at fast synapses in the mammalian brain | Q34406384 | ||
Direct observation of the three-state folding of a single protein molecule | Q34453219 | ||
Nanomechanical measurements of the sequence-dependent folding landscapes of single nucleic acid hairpins | Q34597333 | ||
Mutant SNAP25B causes myasthenia, cortical hyperexcitability, ataxia, and intellectual disability | Q34777891 | ||
Three αSNAP and 10 ATP molecules are used in SNARE complex disassembly by N-ethylmaleimide-sensitive factor (NSF) | Q35002875 | ||
The RSC chromatin remodelling ATPase translocates DNA with high force and small step size | Q35048885 | ||
Mechanistic insights into the recycling machine of the SNARE complex | Q35058666 | ||
A mutation in the Golgi Qb-SNARE gene GOSR2 causes progressive myoclonus epilepsy with early ataxia | Q35136950 | ||
Multiple conformations of a single SNAREpin between two nanodisc membranes reveal diverse pre-fusion states | Q35532161 | ||
Spring-loaded unraveling of a single SNARE complex by NSF in one round of ATP turnover | Q35636093 | ||
Kinetically coupled folding of a single HIV-1 glycoprotein 41 complex in viral membrane fusion and inhibition | Q35699218 | ||
Single-molecule observation of helix staggering, sliding, and coiled coil misfolding | Q35889460 | ||
Reconstituting Intracellular Vesicle Fusion Reactions: The Essential Role of Macromolecular Crowding | Q36263474 | ||
Regulation of membrane fusion by the membrane-proximal coil of the t-SNARE during zippering of SNAREpins | Q36323855 | ||
v-SNARE transmembrane domains function as catalysts for vesicle fusion | Q42382355 | ||
One SNARE complex is sufficient for membrane fusion | Q42531466 | ||
Phase transition behavior of single phosphatidylcholine bilayers on a solid spherical support studied by DSC, NMR and FT-IR | Q42582995 | ||
Reversible unfolding of single RNA molecules by mechanical force | Q43590684 | ||
SNARE assembly and disassembly exhibit a pronounced hysteresis | Q43851628 | ||
A transient N-terminal interaction of SNAP-25 and syntaxin nucleates SNARE assembly | Q44686474 | ||
Role of an N-ethylmaleimide-sensitive transport component in promoting fusion of transport vesicles with cisternae of the Golgi stack | Q46341560 | ||
On the value of c: can low affinity systems be studied by isothermal titration calorimetry? | Q47357121 | ||
The principle of membrane fusion in the cell (Nobel lecture). | Q48069250 | ||
Fast vesicle fusion in living cells requires at least three SNARE complexes. | Q50541149 | ||
Direct observation of transition paths during the folding of proteins and nucleic acids. | Q53112464 | ||
Synaptotagmin-1 Docks Secretory Vesicles to Syntaxin-1/SNAP-25 Acceptor Complexes | Q56992446 | ||
DNA-Induced Programmable Fusion of Phospholipid Vesicles | Q57365828 | ||
Inhibition of SNARE Complex Assembly Differentially Affects Kinetic Components of Exocytosis | Q57978998 | ||
v-SNARE Actions during Ca2+-Triggered Exocytosis | Q58343442 | ||
N- to C-Terminal SNARE Complex Assembly Promotes Rapid Membrane Fusion | Q63610158 | ||
Activity-dependent changes in partial VAMP complexes during neurotransmitter release | Q73202435 | ||
Energetics and dynamics of SNAREpin folding across lipid bilayers | Q81376037 | ||
Membrane-proximal tryptophans of synaptobrevin II stabilize priming of secretory vesicles | Q85392206 | ||
Membrane interactions of fusogenic coiled-coil peptides: implications for lipopeptide mediated vesicle fusion | Q88050467 | ||
Protein-DNA chimeras for single molecule mechanical folding studies with the optical tweezers | Q40311799 | ||
α-SNAP interferes with the zippering of the SNARE protein membrane fusion machinery | Q40370953 | ||
Exocytosis requires asymmetry in the central layer of the SNARE complex | Q40388114 | ||
α-SNAP Enhances SNARE Zippering by Stabilizing the SNARE Four-Helix Bundle. | Q40408922 | ||
Neurotransmitter release - four years of SNARE complexes | Q41541527 | ||
A conserved membrane attachment site in alpha-SNAP facilitates N-ethylmaleimide-sensitive factor (NSF)-driven SNARE complex disassembly. | Q41868502 | ||
SNARE proteins: one to fuse and three to keep the nascent fusion pore open | Q41920045 | ||
Is assembly of the SNARE complex enough to fuel membrane fusion? | Q42059651 | ||
Synaptobrevin N-terminally bound to syntaxin-SNAP-25 defines the primed vesicle state in regulated exocytosis | Q42176873 | ||
A direct role for the Sec1/Munc18-family protein Vps33 as a template for SNARE assembly | Q42288650 | ||
Structure and function of SNARE and SNARE-interacting proteins | Q36335459 | ||
Close is not enough: SNARE-dependent membrane fusion requires an active mechanism that transduces force to membrane anchors | Q36342484 | ||
The trans-SNARE-regulating function of Munc18-1 is essential to synaptic exocytosis | Q36344941 | ||
Synaptic proteins promote calcium-triggered fast transition from point contact to full fusion | Q36446947 | ||
Structure-Based Derivation of Protein Folding Intermediates and Energies from Optical Tweezers | Q36495463 | ||
Lipid-anchored Synaptobrevin Provides Little or No Support for Exocytosis or Liposome Fusion. | Q36548383 | ||
Munc18-1-regulated stage-wise SNARE assembly underlying synaptic exocytosis | Q36552655 | ||
Exocytotic fusion pores are composed of both lipids and proteins | Q36589148 | ||
Calculating Transition Energy Barriers and Characterizing Activation States for Steps of Fusion | Q36678687 | ||
Snapshot of sequential SNARE assembling states between membranes shows that N-terminal transient assembly initializes fusion | Q36770797 | ||
Overstretching B-DNA: the elastic response of individual double-stranded and single-stranded DNA molecules | Q36798786 | ||
Highly anisotropic stability and folding kinetics of a single coiled coil protein under mechanical tension | Q36897066 | ||
Membrane fusion intermediates via directional and full assembly of the SNARE complex | Q36916260 | ||
Nanodisc-cell fusion: control of fusion pore nucleation and lifetimes by SNARE protein transmembrane domains | Q36970468 | ||
Complexin induces a conformational change at the membrane-proximal C-terminal end of the SNARE complex | Q37052763 | ||
Effects of linker sequences on vesicle fusion mediated by lipid-anchored DNA oligonucleotides | Q37079079 | ||
Recent advances in optical tweezers | Q37096963 | ||
Molecular form follows function: (un)snaring the SNAREs | Q37233520 | ||
Capture and release of partially zipped trans-SNARE complexes on intact organelles | Q37237653 | ||
Kinetic barriers to SNAREpin assembly in the regulation of membrane docking/priming and fusion. | Q37281549 | ||
Complexin-1 enhances the on-rate of vesicle docking via simultaneous SNARE and membrane interactions | Q37370388 | ||
Stability, folding dynamics, and long-range conformational transition of the synaptic t-SNARE complex | Q37514982 | ||
Conflicting views on the membrane fusion machinery and the fusion pore | Q37540115 | ||
A half-zippered SNARE complex represents a functional intermediate in membrane fusion. | Q37701673 | ||
Molecular mechanisms for synchronous, asynchronous, and spontaneous neurotransmitter release | Q38166028 | ||
The molecular machinery of neurotransmitter release (Nobel lecture). | Q38262070 | ||
Control of membrane gaps by synaptotagmin-Ca2+ measured with a novel membrane distance ruler | Q38302250 | ||
SNARE complex formation is triggered by Ca2+ and drives membrane fusion | Q38325384 | ||
SNARE protein analog-mediated membrane fusion. | Q38413709 | ||
SNARE and regulatory proteins induce local membrane protrusions to prime docked vesicles for fast calcium-triggered fusion. | Q38798689 | ||
Chaperoning SNARE assembly and disassembly | Q38865222 | ||
Hidden Markov Modeling with Detailed Balance and Its Application to Single Protein Folding | Q39183266 | ||
Single-Molecule Protein Folding Experiments Using High-Precision Optical Tweezers | Q39187447 | ||
Extension of Helix 12 in Munc18-1 Induces Vesicle Priming. | Q39643764 | ||
P433 | issue | 7 | |
P921 | main subject | optical tweezers | Q1066633 |
P304 | page(s) | 1252-1265 | |
P577 | publication date | 2017-03-08 | |
P1433 | published in | Protein Science | Q7251445 |
P1476 | title | Energetics, kinetics, and pathway of SNARE folding and assembly revealed by optical tweezers | |
P478 | volume | 26 |
Q47210280 | Editorial Overview: Single-Molecule Approaches up to Difficult Challenges in Folding and Dynamics |
Q41540634 | Integrated Method to Attach DNA Handles and Functionally Select Proteins to Study Folding and Protein-Ligand Interactions with Optical Tweezers |
Q92725689 | Mutations in the Neuronal Vesicular SNARE VAMP2 Affect Synaptic Membrane Fusion and Impair Human Neurodevelopment |
Q61806540 | SNARE machinery is optimized for ultrafast fusion |
Q57454615 | Single-Molecule Optical Tweezers Study of Regulated SNARE Assembly |
Q56876830 | Switching of the folding-energy landscape governs the allosteric activation of protein kinase A |
Q64229653 | Symmetrical organization of proteins under docked synaptic vesicles |
Q60951140 | The Complex Conformational Dynamics of Neuronal Calcium Sensor-1: A Single Molecule Perspective |
Q47423503 | Two Disease-Causing SNAP-25B Mutations Selectively Impair SNARE C-terminal Assembly |