TY - JOUR
T1 - Flattening and shrinkage of bacteriophage T7 after preparation for electron microscopy by negative staining
AU - Serwer, Philip
N1 - Funding Information:
For valuable criticism during the course of this work, I thank John Ruark~ Dr. Darrell R. Jackson, and Dr. J. P. Revel. I also thank Dr. J. Vinograd for allowing me access to the computer and microcom-parator used in this study and Patrick F. Koen for advice on technical matters concerning the electron microscope. Support was received from an American Cancer Society Postdoctoral Fellowship, a grant to Dr. W. B. Wood from the U.S. Public Health Service (AI 02938), an NSF grant to Dr. Robert M. Stroud (BMS 75-04105), and an NSF grant to Dr. J. P. Revel (06965).
PY - 1977/3
Y1 - 1977/3
N2 - A technique for using stereo electron microscopy to determine the degree of flattening and volume of particles embedded in negative stain is developed. Using this technique, it is shown that bacteriophage T7 particles, which have been prepared for electron microscopy by negative staining with uranyl acetate, are considerably flattened. The edge-to-edge diameter of negatively stained phage is 545 ± 20 . Some fields in negatively stained specimens contain T7 phage whose DNA is positively stained, which are surrounded by little or no negative stain. These positively stained phage particles are shown to be less flattened than the negatively stained phage and consequently have a smaller edge-to-edge diameter (457 ± 17 ). The volumes of negatively and positively stained phage (excluding the phage tail) are equal within experimental error to the anhydrous phage volume (4.99 ± 0.15 × 10-17 ml) and are significantly less than the hydrated phage volume (1.14 ± .02 × 10-16 ml, (Ref. 1). Thus, both negatively and positively stained T7 phage have undergone a decrease in volume during preparation for electron microscopy.
AB - A technique for using stereo electron microscopy to determine the degree of flattening and volume of particles embedded in negative stain is developed. Using this technique, it is shown that bacteriophage T7 particles, which have been prepared for electron microscopy by negative staining with uranyl acetate, are considerably flattened. The edge-to-edge diameter of negatively stained phage is 545 ± 20 . Some fields in negatively stained specimens contain T7 phage whose DNA is positively stained, which are surrounded by little or no negative stain. These positively stained phage particles are shown to be less flattened than the negatively stained phage and consequently have a smaller edge-to-edge diameter (457 ± 17 ). The volumes of negatively and positively stained phage (excluding the phage tail) are equal within experimental error to the anhydrous phage volume (4.99 ± 0.15 × 10-17 ml) and are significantly less than the hydrated phage volume (1.14 ± .02 × 10-16 ml, (Ref. 1). Thus, both negatively and positively stained T7 phage have undergone a decrease in volume during preparation for electron microscopy.
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U2 - 10.1016/S0022-5320(77)90015-6
DO - 10.1016/S0022-5320(77)90015-6
M3 - Article
C2 - 66322
AN - SCOPUS:0017625998
SN - 0022-5320
VL - 58
SP - 235
EP - 243
JO - Journal of Ultrasructure Research
JF - Journal of Ultrasructure Research
IS - 3
ER -