TY - JOUR
T1 - A new HPF specimen carrier adapter for the use of high-pressure freezing with cryoscanning electron microscope
T2 - two applications: stearic acid organization in a hydroxypropyl methylcellulose matrix and mice myocardium
AU - Payre, B.
AU - Gontier, E.
AU - Jarray, A.
AU - Martinez, Y.
AU - Laugier, J.P.
AU - Delalleau, A.
AU - Gaillard, B.M.
AU - Anselme, I.
AU - Goudounèche, D.
AU - Fourquaux, I.
AU - Hemati, M.
AU - Gerbaud, V.
AU - Delisle, M.B.
AU - Guilbeau-Frugier, C.
PY - 2018/9
Y1 - 2018/9
N2 - Cryogenic transmission electron microscopy of high-pressure freezing (HPF) samples is a well-established technique for the analysis of liquid containing specimens. This technique enables observation without removing water or other volatile components. The HPF technique is less used in scanning electron microscopy (SEM) due to the lack of a suitable HPF specimen carrier adapter. The traditional SEM cryotransfer system (PP3000T Quorum Laughton, East Sussex, UK; Alto Gatan, Pleasanton, CA, USA) usually uses nitrogen slush. Unfortunately, and unlike HPF, nitrogen slush produces water crystal artefacts. So, we propose a new HPF specimen carrier adapter for sample transfer from HPF system to cryogenic-scanning electronic microscope (Cryo-SEM). The new transfer system is validated using technical two applications, a stearic acid in hydroxypropyl methylcellulose solution and mice myocardium. Preservation of samples is suitable in both cases. Cryo-SEM examination of HPF samples enables a good correlation between acid stearic liquid concentration and acid stearic occupation surface (only for homogeneous solution). For biological samples as myocardium, cytoplasmic structures of cardiomyocyte are easily recognized with adequate preservation of organelle contacts and inner cell organization. We expect this new HPF specimen carrier adapter would enable more SEM-studies using HPF.
AB - Cryogenic transmission electron microscopy of high-pressure freezing (HPF) samples is a well-established technique for the analysis of liquid containing specimens. This technique enables observation without removing water or other volatile components. The HPF technique is less used in scanning electron microscopy (SEM) due to the lack of a suitable HPF specimen carrier adapter. The traditional SEM cryotransfer system (PP3000T Quorum Laughton, East Sussex, UK; Alto Gatan, Pleasanton, CA, USA) usually uses nitrogen slush. Unfortunately, and unlike HPF, nitrogen slush produces water crystal artefacts. So, we propose a new HPF specimen carrier adapter for sample transfer from HPF system to cryogenic-scanning electronic microscope (Cryo-SEM). The new transfer system is validated using technical two applications, a stearic acid in hydroxypropyl methylcellulose solution and mice myocardium. Preservation of samples is suitable in both cases. Cryo-SEM examination of HPF samples enables a good correlation between acid stearic liquid concentration and acid stearic occupation surface (only for homogeneous solution). For biological samples as myocardium, cytoplasmic structures of cardiomyocyte are easily recognized with adequate preservation of organelle contacts and inner cell organization. We expect this new HPF specimen carrier adapter would enable more SEM-studies using HPF.
KW - Cryogenic fracture
KW - Cryogenic freezing
KW - Cryogenic scanning electron microscopy
KW - High-pressure freezing
KW - HPF specimen carrier adapter
U2 - 10.1111/jmi.12713
DO - 10.1111/jmi.12713
M3 - Article
C2 - 29901222
AN - SCOPUS:85051868882
SN - 0022-2720
VL - 271
SP - 255
EP - 265
JO - Journal of Microscopy
JF - Journal of Microscopy
IS - 3
ER -