• No results found

Biological nanopores having tunable pore diameters and uses thereof as analytical tools

N/A
N/A
Protected

Academic year: 2021

Share "Biological nanopores having tunable pore diameters and uses thereof as analytical tools"

Copied!
53
0
0

Bezig met laden.... (Bekijk nu de volledige tekst)

Hele tekst

(1)

University of Groningen

Biological nanopores having tunable pore diameters and uses thereof as analytical tools

Huang, Gang; Maglia, Giovanni

IMPORTANT NOTE: You are advised to consult the publisher's version (publisher's PDF) if you wish to cite from

it. Please check the document version below.

Document Version

Publisher's PDF, also known as Version of record

Publication date:

2020

Link to publication in University of Groningen/UMCG research database

Citation for published version (APA):

Huang, G., & Maglia, G. (2020). Biological nanopores having tunable pore diameters and uses thereof as

analytical tools. (Patent No. WO2020055246).

Copyright

Other than for strictly personal use, it is not permitted to download or to forward/distribute the text or part of it without the consent of the author(s) and/or copyright holder(s), unless the work is under an open content license (like Creative Commons).

Take-down policy

If you believe that this document breaches copyright please contact us providing details, and we will remove access to the work immediately and investigate your claim.

Downloaded from the University of Groningen/UMCG research database (Pure): http://www.rug.nl/research/portal. For technical reasons the number of authors shown on this cover page is limited to 10 maximum.

(2)
(3)
(4)
(5)
(6)
(7)
(8)
(9)
(10)
(11)
(12)
(13)
(14)
(15)
(16)
(17)
(18)
(19)
(20)
(21)
(22)
(23)
(24)
(25)
(26)
(27)
(28)
(29)
(30)
(31)
(32)
(33)
(34)
(35)
(36)
(37)
(38)
(39)
(40)
(41)
(42)
(43)
(44)
(45)
(46)
(47)
(48)
(49)
(50)
(51)
(52)
(53)

Referenties

GERELATEERDE DOCUMENTEN

Electro-osmotic capture and ionic discrimination of peptide and protein biomarkers with FraC nanopores 1.. Protein capture with FraC

The Guan group mutated the constriction (M113, T145) of α-hemolysin to tyrosine (Y) and phenylalanine (F) and showed that peptides composed of just a few aromatic amino acids

Finally, angiotensin 1 translocated at all potentials tested (Figure 3e). The dwell time of angiotensin 1 was close to the limit of detection, thus most likely angiotensin

These and several addition lines of evidence (Supplementary note 1, Figure S6) strongly suggest that the three types of FraC nanopores represent nanopores with different

Supported by directed evolution, we precisely engineered the constriction of the nanopore to generate an electroosmotic flow that permitted the efficient capture

More importantly, there should be a correlation between the nanopore ionic current signal and peptides mass if we ought to identify an unknown peptide to make the nanopore

Door de pH te verlagen tot 3.8 hebben we bovendien een correlatie waargenomen tussen de uitgesloten stroom en de peptidemassa voor alle peptiden die we hebben getest.. Met

[r]