Literature DB >> 19078936

Pressure-polishing pipettes for improved patch-clamp recording.

Brandon E Johnson1, Austin L Brown, Miriam B Goodman.   

Abstract

Pressure-polishing is a method for shaping glass pipettes for patch-clamp recording. We first developed this method for fabricating pipettes suitable for recording from small (<3 m) neuronal cell bodies. The basic principal is similar to glass-blowing and combines air pressure and heat to modify the shape of patch pipettes prepared by a conventional micropipette puller. It can be applied to so-called soft (soda lime) and hard (borosilicate) glasses. Generally speaking, pressure polishing can reduce pipette resistance by 25% without decreasing the diameter of the tip opening (Goodman and Lockery, 2000). It can be applied to virtually any type of glass and requires only the addition of a high-pressure valve and fitting to a microforge. This technique is essential for recording from ultrasmall cells (<5 m) and can also improve single-channel recording by minimizing pipette resistance. The blunt shape is also useful for perforated-patch clamp recording since this tip shape results in a larger membrane bleb available for perforation.

Entities:  

Mesh:

Year:  2008        PMID: 19078936      PMCID: PMC3234038          DOI: 10.3791/964

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  1 in total

1.  Pressure polishing: a method for re-shaping patch pipettes during fire polishing.

Authors:  M B Goodman; S R Lockery
Journal:  J Neurosci Methods       Date:  2000-07-31       Impact factor: 2.390

  1 in total
  7 in total

1.  Tissue mechanics govern the rapidly adapting and symmetrical response to touch.

Authors:  Amy L Eastwood; Alessandro Sanzeni; Bryan C Petzold; Sung-Jin Park; Massimo Vergassola; Beth L Pruitt; Miriam B Goodman
Journal:  Proc Natl Acad Sci U S A       Date:  2015-12-01       Impact factor: 11.205

2.  A pressure-polishing set-up to fabricate patch pipettes that seal on virtually any membrane, yielding low access resistance and efficient intracellular perfusion.

Authors:  Mascia Benedusi; Marco Aquila; Alberto Milani; Giorgio Rispoli
Journal:  Eur Biophys J       Date:  2011-07-15       Impact factor: 1.733

3.  Electrophysiological methods for Caenorhabditis elegans neurobiology.

Authors:  Miriam B Goodman; Theodore H Lindsay; Shawn R Lockery; Janet E Richmond
Journal:  Methods Cell Biol       Date:  2012       Impact factor: 1.441

4.  Serotonin differentially modulates Ca2+ transients and depolarization in a C. elegans nociceptor.

Authors:  Jeffrey A Zahratka; Paul D E Williams; Philip J Summers; Richard W Komuniecki; Bruce A Bamber
Journal:  J Neurophysiol       Date:  2014-11-19       Impact factor: 2.714

5.  GCY-8, PDE-2, and NCS-1 are critical elements of the cGMP-dependent thermotransduction cascade in the AFD neurons responsible for C. elegans thermotaxis.

Authors:  Dong Wang; Damien O'Halloran; Miriam B Goodman
Journal:  J Gen Physiol       Date:  2013-10       Impact factor: 4.086

Review 6.  Advanced real-time recordings of neuronal activity with tailored patch pipettes, diamond multi-electrode arrays and electrochromic voltage-sensitive dyes.

Authors:  Bernd Kuhn; Federico Picollo; Valentina Carabelli; Giorgio Rispoli
Journal:  Pflugers Arch       Date:  2020-10-13       Impact factor: 3.657

7.  Functional subgroups of cochlear inner hair cell ribbon synapses differently modulate their EPSC properties in response to stimulation.

Authors:  Mamiko Niwa; Eric D Young; Elisabeth Glowatzki; Anthony J Ricci
Journal:  J Neurophysiol       Date:  2021-05-05       Impact factor: 2.714

  7 in total

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